SUMMARY
Liver-specific knockout of Nrf1 in mice leads to non-alcoholic steatohepatitis with dyslipidemia, and its deterioration results in spontaneous hepatoma, but the underlying mechanism remains elusive. A similar pathological model is herein reconstructed by using human Nrf1α-specific knockout cell lines. We demonstrated that a marked increase of the inflammation marker COX2 in Nrf1α−/− cells. Loss of Nrf1α leads to hyperactivation of Nrf2, which results from substantial decreases in both Keap1 and PTEN in Nrf1α−/− cells. Further investigation of xenograft mice showed that malignant growth of Nrf1α−/−-derived tumor is almost abolished by silencing Nrf2, while Nrf1α+/+-tumor is markedly repressed by inactive Nrf2−/−ΔTA, but unaffected by a priori constitutive activator of caNrf2ΔN. Mechanistic studies unraveled there exist opposing and unifying inter-regulatory cross-talks between Nrf1 and Nrf2. Collectively, Nrf1α manifests a dominant tumor-suppressive effect by confining Nrf2 oncogenicity, while Nrf2 can directly activate the transcriptional expression of Nrf1 to form a negative feedback loop.
HIGHLIGHTS
Opposing and unifying inter-regulatory cross-talks between Nrf1α and Nrf2
Malignant growth of Nrf1α−/−-derived tumor is prevented by silencing Nrf2
Hyper-activation of Nrf2 by Nrf1α−/− results from decreased Keap1 and PTEN
Nrf1α+/+-tumor is repressed by Nrf2−/−ΔTA, but unaltered by its active caNrf2ΔN
INTRODUCTION
The steady-state lipid levels are crucial for maintaining cellular and organismal homeostasis, not only in term of energy metabolism, but also to prevent potential cytotoxity. Conversely, excessive nutrients (and metabolic stress) can culminate in a series of severe diseases such as diabetes, obesity and fatty liver. Notably, non-alcoholic fatty liver disease (NAFLD) affects 25% of global population, up to 80% of obese people having this disease (Corte et al., 2015; Younossi et al., 2018). NAFLD comprises a continuum series of pathological conditions varying in severity of liver injury and exacerbation. Among them, non-alcoholic steatohepatitis (NASH) is defined as a serious process with inflammation and hepatocyte damage, and also hence regarded as a major cause of liver fibrosis, cirrhosis, and even cancer, such as hepatocellular carcinoma (HCC), among those caused by unknown etiologies (Friedman et al., 2018; Michelotti et al., 2013; Rowell and Anstee, 2015; Wong et al., 2018). However, the axiomatic mechanisms underlying development of NASH and malignant transformation into hepatoma remain elusive.
The cumulative evidence obtained from distinct animal models resembling human NASH (Friedman et al., 2018) demonstrates that homeostatic and nutrient-stimulated lipid metabolisms are tightly regulated by multiple layers of diverse signaling to transcription factor networks to monitor precision expression of target genes (Jump et al., 2013; Karagianni and Talianidis, 2015). Among them, SREBP1c (sterol-regulatory element binding protein 1c) is established as a key marker and therapeutic target for hepatosteatosis, because transgenic over-expression of this factor leads to hepatosteatosis, but not hepatoma (Nakayama et al., 2007). Yet, similar hyperactivation of SREBP1c by knockout of GP78, an endoplasmic reticulum (ER) membrane-bound E3 ligase, occurs with age-related obesity, NASH and HCC (Zhang et al., 2015a). Conversely, hepatosteatosis is partially mitigated by the deficiency of SREBP1c (Yahagi et al., 2002), but sufficiently ameliorated by blockage of SREBP processing by deletion of SCAP (SREBP cleavage-activating protein) (Moon et al., 2012). These findings indicate an additive involvement of other factors beyond SREBPs in NASH-associated malignant pathology.
Interestingly, spontaneous NASH with massive hepatomegaly and hepatoma results from the hepatocyte-specific knockout of PTEN (phosphatase and tensin homolog, a well-known tumor repressor) in mice (Horie et al., 2004). Loss of PTEN leads to constitutive activation of the phosphatidylinositol 3-kinases (PI3K)-AKT-mTOR pathway so as to augment expression of metabolic genes regulated by SREBP1c and PPARγ in cancer proliferative cells (Hollander et al., 2011; Lee et al., 2018; Shimano and Sato, 2017). This process is accompanied by nuclear accumulation of Nrf2 (nuclear factor erythroid 2-like 2, also called NFE2L2) in PTEN-deficient cells (Mitsuishi et al., 2012; Sakamoto et al., 2009). Nrf2 and Nrf1 are two principal members of the cap’n’collar (CNC) basic-region leucine zipper (bZIP) family to transactivate antioxidant response element (ARE)-driven genes involved in detoxification, cytoprotection, metabolism and proliferation. Significantly, aberrant accumulation of Nrf2 and activation of target genes are significantly incremented by simultaneous deletion of PTEN (leading to a GSK3β-directed phosphodegron of Nrf2 targeting this CNC-bZIP protein to the β-TrCP-based E3 ubiquitin ligase Cullin 1-mediated proteasomal degradation) and Keap1 (acting as an adaptor targeting Nrf2 to the Cullin 3-mediated proteasomal degradation), resulting in a deterioration of PTEN−/−-leading cancer pathology (Best et al., 2018; Rojo et al., 2014; Taguchi et al., 2014). Conversely, malignant transformation of double PTEN:Keap1 knockout mice is alleviated by additive deletion of Nrf2 (Taguchi et al., 2014), implying Nrf2 promotes carcinogenesis. This is consistent with further observations that activity of Nrf2 is required for oncogenic KRAS-driven tumorigenesis (DeNicola et al., 2011) and its activation by antidiabetic agents accelerates tumor metastasis in xenograft models (Wang et al., 2016). However, non-neoplastic lesions are caused by constitutive active Nrf2 (caNrf2) mutants lacking the Keap1-binding sites in transgenic mice (Schafer et al., 2010; Shanmugam et al., 2017), but their cytoprotection against carcinogenesis is enhanced. Further investigation of a dominant-negative dnNrf2 mutant (also suppresses other CNC-bZIP factors, such as Nrf1) has demonstrated that the basal ARE-driven gene expression, but not their inducible expression, is crucial for anti-tumor chemoprevention against the chemical-induced carcinogenesis (auf dem Keller et al., 2006). Yet, the underlying mechanism by which Nrf2 is determined to exert dual opposing roles in tumor suppression or promotion remains unknown to date.
Significantly, another phenotype of spontaneous NASH and hepatoma is manifested in conditional Nrf1−/− mice, displaying a bulk of lipid drops in the ER with dramatic morphological changes (Ohtsuji et al., 2008; Xu et al., 2005). Global knockout mice of Nrf1−/− die of severe oxidative stress-induced damages and fetal liver hypoplasia during development (Chan et al., 1998; Chen et al., 2003). By contrast, global Nrf2−/− knockout mice are viable and fertile, without any obvious pathological phenotypes occurring during normal growth and development (Itoh et al., 1997). Such facts indicate that Nrf1 is not compensated by Nrf2, although both are widely co-expressed in various tissues and have similar overlapping roles in coordinately regulating ARE-driven genes. Further insights also reveal that Nrf1 exerts unique essential functions, which are distinctive from Nrf2, in maintaining cellular redox, lipid and protein homeostasis, as well as organ integrity, through regulation of distinct target genes (Bugno et al., 2015; Zhang and Xiang, 2016). This is reinforced by further investigation of other organ-specific Nrf1 deficiency or over-activation in mice, which exhibit distinct pathological phenotypes, such as type 2 diabetes, neurodegenerative and cardiovascular disease (Hirotsu et al., 2014; Kobayashi et al., 2011; Lee et al., 2011; Zheng et al., 2015). In addition to functionality of Nrf1 as an indispensable CNC-bZIP transcription factor, it is also identified to act as a directly ER membrane-bound sensor to govern cholesterol homeostasis through the consensus recognition motifs (Widenmaier et al., 2017; Zhang et al., 2014b) and lipid distribution in distinct tissues (Bartelt et al., 2018; Hou et al., 2018). However, it is regrettable to unclearly define which isoforms of Nrf1 are required to execute its unique physio-pathological functions, because almost all isoforms of the factor are disrupted to varying extents in the above-described experimental models.
Upon translation of Nrf1, its N-terminal ER-targeting signal anchor enables the nascent full-length protein Nrf1α to be topologically integrated within and around the membranes, while other domains of the CNC-bZIP protein are partitioned on the luminal or cytoplasmic sides (Zhang et al., 2007b; Zhang et al., 2014b). Subsequently, some luminal-resident domains of Nrf1α are dynamically repositioned across membranes through a p97-driven retrotranslocation pathway (Radhakrishnan et al., 2014; Sha and Goldberg, 2014; Zhang et al., 2015b). In these topovectorial processes of Nrf1α, it is subjected to specific post-translational modifications (e.g. glycosylation, deglycosylation, ubiquitination), and also selective juxtamembrane proteolytic processing of the CNC-bZIP factor so as to yield multiple isoforms with different and opposing activities, during maturation into an activator (Koizumi et al., 2016; Xiang et al., 2018a; Xiang et al., 2018b). In addition, distinct variants of Nrf1, including its long TCF11, short Nrf1β/LCR-F1 and small dominant-negative Nrf1γ/δ, are also generated by alternative translation from various lengths of alternatively-spliced mRNA transcripts (Zhang et al., 2014a). Yet, each Nrf1 isoform-specific physiological function virtually remains obscure.
Notably, specific gene-editing knockout of Nrf1α leads to a significant increase in the malignant proliferation of Nrf1α−/−-derived hepatoma and the tumor metastasis to the liver in xenograft model mice (Ren et al., 2016). This work reveals that Nrf1α may act as a tumor suppressor, but the underlying mechanism remains unclear. Herein, our present work further unravels that Nrf1 and Nrf2 have mutual opposing and unified inter-regulatory cross-talks towards downstream genes. For instance, aberrant hyperactivation of Nrf2 leads to a constitutive increase of its target cycloxygenase-2 (COX2) in Nrf1α−/− cells. Such hyper-activation of Nrf2 by knockout of Nrf1α is accompanied by substantial decreases in both Keap1 and PTEN. The malignant growth of Nrf1α−/−-derived tumor is significantly prevented by knockdown of Nrf2, while Nrf1α+/+-bearing tumor is also markedly suppressed by knockout of Nrf2, but unaffected by a priori constitutive activator of Nrf2 (i.e. caNrf2ΔN). Such distinct phenotypes of animal xenograft tumors are determined by differential expression of different subsets of genes regulated by Nrf1α or Nrf2 alone or both. These collective findings demonstrated that Nrf1α manifests as a dominant tumor-suppressor to confine Nrf2 oncogenicity. Conversely, though Nrf2 acts as a tumor promoter, it directly mediates the transcriptional expression of Nrf1 so as to form a negative feedback loop.
RESULTS
The human Nrf1α−/− -and Nrf2−/−ΔTA-driven cell models are established
Since the phenotypes of liver-specific Nrf1−/− mice resemble human pathogenesis of hepatic steatosis, NASH and HCC (Ohtsuji et al., 2008; Tsujita et al., 2014; Xu et al., 2005), this is thus inferred available for exploring the underlying mechanisms whereby NASH is transformed for the malignant progression towards hepatoma (Figure 1A). However, it is unknown whether human Nrf1α exerts similar effects to those obtained from the aforementioned mouse models. For this end, a similar pathological model was here recapitulated by genome-editing knockout of Nrf1α from human HepG2 cells, aiming to elucidate the mechanism by which a non-resolving NASH-based inflammation is exacerbated. To achieve the genomic locus-specific knockout of Nrf1α, we created a pair of TALEN-directed constructs to yield a specific deletion of Nrf1α-derived isoforms from the single Nfe2l1 gene, but with shorter variants Nrf1β to Nrf1δ unaffected (Figures 1B and S1A). In the parallel experiments, another pair of CRISPR/cas9-mediated constructs were engineered to delete the Nrf2-specific codons (covering its 42-175 amino acids within essential Keap1-binding and most of its transactivation domains) from the Nef2l2 gene to yield an inactive mutant Nrf2−/−ΔTA (Figures 1D, 1E and S1B). Consequently, two monoclonal hepatoma cell lines of Nrf1α−/− and Nrf2−/−ΔTA were, respectively, established and confirmed to be true by sequencing their genomic DNAs, and Western blotting with specific antibodies (Figure 1, B to E). Further real-time qPCRs with specific primers that recognized distinct nucleotide fragments showed that knockout of Nrf1α substantially abolished expression of total Nrf1 mRNAs in Nrf1α−/− cells (Figure 1B, right panel). Similar results were also obtained from other clones of Nrf1α−/− cell lines (Ren et al., 2016). Notably, Nrf2−/−ΔTA cells gave rise to an inactive mutant lacking nt124-526 of Nrf2, but the expression of its DNA-binding domains (DBD)-containing mRNA transcripts was unaltered (Figure 1D, right panel). Therefore, the resulting inactive mutant Nrf2ΔTA polypeptides may still, theoretically, bind Nrf2-target genes, and also circumvent competitive occupancy with other complementary factors, upon loss of the prototypic Nrf2.
A plausible explanation of NASH pathogenesis is preferred to the classic two-hit hypothesis, in which the first hit is hepatosteatosis (caused by the accumulation of cholesterol and lipids), and the second hit is inflammation (induced by oxidative stress) (Friedman et al., 2018; Shimano and Sato, 2017). Such being the case, we next examine whether Nrf1α−/− cells act accordingly. As anticipated, it is illustrated by measuring intracellular hydrogen peroxide as a representative of reactive oxygen species (ROS), that endogenous oxidative stress was strikingly induced in Nrf1α−/− cells, but slightly relieved by inactive Nrf2−/−ΔTA, when compared with wild-type Nrf1/2+/+ progenitor cells (Figure 1F). Subsequently, a significant accumulation of lipids was seen after staining of Nrf1α−/− cells, by comparison with Nrf2−/−ΔTA and Nrf1/2+/+ cells (Figure 1G). With increasing time of oleic acid (OA) treatment to 7 days, the lipid accumulation was significantly incremented in Nrf1α−/− cells to a maximum ∼182-fold estimated. While compared with ∼60-fold accumulation of lipids in Nrf1/2+/+ cells, the overload was substantially alleviated by inactive Nrf2−/−ΔTA to ∼34-fold (Figure 1, G & H).
In addition to lipid metabolic disorders resulting from loss of Nrf1’s function to regulate LPIN1, PGC-1β and other metabolic genes (Hirotsu et al., 2012; Tsujita et al., 2014), NASH has a not-yet-identified characteristic of refractory inflammation. Accordingly, we determined the transcriptional expression of key genes encoding cytokines and relevant receptors involved in putative inflammatory responses. As expected, expression of all nine examined genes encoding IL-1A, IL-1B, IL-1R1, IL-1R2, IL-6, IL-8, IL-10, TGF1α, and TGF1β was significantly elevated in Nrf1α−/− cells (Figure 1I). By contrast with Nrf1/2+/+ cells, mRNA expression of IL-1A, IL-1R2, IL-6 and IL-8 was markedly down-regulated by inactive Nrf2−/−ΔTA, while both IL-1B and IL-10 expression was still marginally up-regulated, but with no changes in other genes (Figure 1I). Collectively, these data demonstrate that the NASH-prone phenotypes are recapitulated by employing human Nrf1α−/−-driven cells, in which Nrf2 may also be critical for this pathogenesis.
The inflammation marker COX2 is up-regulated, while COX1 is down-regulated, in Nrf1α−/− cells
Development of inflammation (e.g. NASH) and malignant transformation into carcinogenesis have a clear relevance to lipid peroxidation, and particularly degradation metabolites of arachidonic acid (AA), such as prostaglandins (PGs), thromboxanes (TXs) and leukotrienes (LTs) (Castellone et al., 2005; Chowdhry et al., 2010; Gupta and Dubois, 2001). In the AA metabolism network, cyclooxygenase 1 (COX1) and COX2 are the rate-limiting enzymes that convert AA into PGs, of which COX2 is considered as a key inflammation marker (Wang and Dubois, 2010) and also identified as a direct target of Nrf2 (Itoh et al., 2004; Sherratt et al., 2003). Since Nrf2 (and Nrf1) can be recruited to directly bind the ARE-containing promoters of COX2 and COX1 before transactivating both genes, it is thereby hypothesized that hyper-expression of the inflammation-related genes in Nrf1α−/− cells is attributable to overstimulation of PG and TX products from the catalyzation by COX2 and COX1 (Figure 1J). To address this, we here examined whether (and how) key rate-limiting enzymes in AA metabolism are influenced by loss of Nrf1α or Nrf2 functions.
As anticipated, a real-time qPCR analysis revealed that mRNA levels of COX1 were almost completely abolished in Nrf1α−/− cells, but obviously increased in Nrf2−/−ΔTA cells by comparison to those obtained from wild-type Nrf1/2+/+ cells (Figure 2A). Contrarily, expression of COX2 was substantially augmented in Nrf1α−/− cells, but almost unaffected by inactive Nrf2−/−ΔTA when compared to the value in Nrf1/2+/+ cells. Furthermore, expression of ALOX5 and FLAP in Nrf1α−/− cells was up-regulated at much higher levels than those measured in Nrf2−/−ΔTA cells at considerable levels (Figure 2A). Next, whether such differences in expression of the AA metabolism genes are attributable to differential and even opposing regulation by Nrf1 and Nrf2 was further examined. Consistently, almost no protein expression of COX1 was detected in Nrf1α−/− cells, while the abundances of COX2 and ALOX5 proteins were significantly increased, when compared with Nrf1/2+/+ cells (Figure 2B). However, COX1 was highly expressed in Nrf2−/−ΔTA cells at a greater level than that obtained from wild-type cells (Figure 2C). Conversely, COX2 was substantially diminished or abolished by the inactive mutant Nrf2−/−ΔTA, whereas ALOX5 was almost unaffected (Figure 2C).
Since COX1 is constitutive essential for normal physiological homeostasis, while COX2 is an inducibly expressed enzyme to be stimulated by inflammatory stress (O’Banion, 1999; Tanabe and Tohnai, 2002), the changing trends of COX2 induction by 12-O-Tetradecanoylphorbol-13-acetate (TPA) stimulation are evaluated. As a result, stimulation of Nrf1/2+/+ cells by TPA caused an obvious induction of COX2 expression to a ∼14-fold maximum at 2 h after treatment; this value was being maintained to 4 h, before being gradually decreased to a ∼5-fold level by 10-h treatment (Figure 2D, 2E). In Nrf1α−/− cells, the constitute up-expression of COX2 was set to 18-fold as its starting point, subsequent incremental abundances of this enzymatic protein were further induced to a maximum of ∼190-fold by 10-h TPA treatment and maintained before the experiment was terminated (Figure 2E,red curve). Relatively, a weak response of COX2 to TPA stimulation of Nrf2−/−ΔTA cells was also observed from 2 h to 8 h, with an inducible peak at 4 h after treatment (Figure 2E, blue curve). Further assays of the luciferase reporter PCOX2-Luc (in which the 2078-bp promoter COX2 gene was constructed) revealed that transcriptional expression of the reporter gene was induced at 4 h after TPA treatment of Nrf1α−/− cells, and the TPA-stimulated increases were continuously maintained until 24 h (Figure S2A, S2B). However, no obvious changes in the PCOX2-Luc activity were detected in TPA-treated Nrf2−/−ΔTA or Nrf1/2+/+ cells. These collective findings imply a striking disparity in Nrf1α-and Nrf2-mediated induction of COX2 by TPA.
Hyper-expression of COX2 results from increased Nrf2 and JNK-mediated AP-1 in Nrf1α−/− cells
Intriguingly, the abundance of COX2, as a well-known direct target of Nrf2, was not decreased, but rather marginally increased by ectopic expression of Nrf1 that had been restored into Nrf1α−/− cells (Figure 2F), in which expression of COS-1 was also rescued, albeit both genes encompass the ARE sites recognized by Nrf1 and Nrf2 (Itoh et al., 2004; Sherratt et al., 2003). These seemingly paradoxical results, along with the above-described data from Nrf1α−/− cells, suggest that Nrf1α may have an ambivalent relationship with Nrf2 in regulating COX1 and COX2 genes. Rather, this confusing but exciting finding arouses our de facto curiosity to explore which possible pathways enable Nrf1 to indirectly regulate COX2 (Figure S3A), albeit this enzyme has been shown to be monitored by CREB, NF-κB, STAT1, FOXM1, ETS1, ELF3 and JNK-regulated AP1 (Ghosh et al., 2007; Grall et al., 2005; Kang et al., 2006; Sharma-Walia et al., 2010; Xu and Shu, 2013; Zhang et al., 2007a). Consequently, the real-time qPCR analysis revealed that mRNA levels of only RELB, but not other members of the NF-κB family (that regulates cellular responses to inflammation), were significantly up-regulated in Nrf1α−/− cells (Figure S3B). This may be coincident with the notion that ablation of an IκB (inhibitor of NF-κB) kinase IKKγ in liver parenchymal cells causes spontaneous NASH and HCC (Luedde et al., 2007). However, Figure S3C showed that the abundance of over-expressed COS2 in Nrf1α−/− cells was unaltered by the caffeic acid phenethyl ester (CAPE, a potent specific inhibitor of NF-κB (Natarajan et al., 1996)), and was also not significantly diminished by JSH-23, a broad spectrum inhibitor of NF-κB (Shin et al., 2004). Thus, it is inferable there implicates an NF-κB-independent pathway to up-regulate expression of COX2 in Nrf1α−/− cells. In addition, it may be not necessary for modest inducible expression of ETS1 (one of the E26 transformation-specific transcription factors), because this was accompanied by substantial down-regulation of another family member ELF3 (Figure S3B).
Further treatments of Nrf1α−/− cells with either of the two CREB inhibitors H-89 and BAPTA-AM (Sharma-Walia et al., 2010; Tymianski et al., 1994) demonstrated that the elevated expression of COX2 was unaffected (Figure S3D). However, it is, to our surprise (Figure S3E), found that the forced abundance of COX2 in Nrf1α−/− cells was sufficiently abolished by a JNK-specific inhibitor SP600125 (Bennett et al., 2001). Further investigations revealed no changes in both mRNA and protein levels of JNK (Figures 2G and S3), but the phosphorylated JNK abundance was significantly increased in Nrf1α−/− cells when compared to those obtained from Nrf1/2+/+ cells (Figure 2G). Therefore, it is initially postulated that Nrf1α−/− cells gave rise to the forced expression of COX2 possibly by activation of JNK signaling. Next, in-depth insights into the signaling of JNK towards downstream target genes unraveled that expression of only c-Jun, but not other examined genes, was significantly elevated in Nrf1α−/− cells (Figures S4B). Further assays of luciferase reporter genes PCOX2-Luc and PTRE-Luc (in which TRE indicates TPA-responsive element inserted within the promoter region) verified that AP-1 (a functional heterodimer of Jun and Fos) is favorably required for the transactivation of COX2 in Nrf1α−/− cells (Figure S4C). By defining distinct AP-1 components (e.g. Jun, Fos, Fra1) at mRNA and protein levels, it is validated that AP-1 was activated in Nrf1α−/− cells, but not in Nrf2−/−ΔTA cells (Figure S4, D to F). In addition, Figure S4G illustrated that hyper-expression of COX2 in Nrf1α−/− cells was not suppressed by AP-1 inhibitor SR11302 (Fanjul et al., 1994). Further knockdown of Jun or Fra1 led to a decrease of COX2, but this was no proportional to the silencing of Jun or Fra1 at lower levels (Figure S4H). All together, AP-1 activation by JNK signaling is involved in, but not essential for making a significant contribution to the reinforced expression of COX2 in Nrf1α−/− cells.
Fortunately, the evidence that expression of Nrf2 and its nuclear translocation are attenuated by JNK inhibitor SP600125 (Ahn et al., 2017; Bak et al., 2016) implicates there exists a direct link between JNK and Nrf2. Consistently, the abundance of Nrf2 protein was surprisingly augmented in Nrf1α−/− cells, which was accompanied by an increase in the phosphorylated JNK (Figure 2G). Similarly, great increases in expression of both COX2 and Nrf2 were caused by knockout of Nrf1α in HL7702Nrf1α−/− (established on the base of the non-cancerous HL7702 hepatocyte line (Figure S5A,B). Further treatments of Nrf1α−/− cells with SP600125 or transfection with Nrf2-targeting siRNA, unraveled that reduction of Nrf2 or JNK appeared to be proportional to the decreased abundance of COX2 (Figure 2H, 2I and S4I). Collectively, these data indicate that the hyper-expression of COX2 in Nrf1α−/− cells is directly caused by increased Nrf2 protein, and the latter CNC-bZIP is also monitored by its upstream JNK signaling. This is supported by the PCOX2- Luc reporter assays showing that Nrf2 mediated transactivation of the COX2 gene driven by its ARE enhancer, because the activation was attenuated by its ARE mutant (i.e. PCOX2m--Luc) (Figure 2J). The transactivation of PCOX2-Luc reporter by Nrf1 (Figure 2J), together with above-described data, indicates that Nrf1α also has one hand to exert a minor positive effect on COX2 by directly binding to its ARE enhancer, but this effect appears to be counteracted by another hand of Nrf1α to elicit a dominant-negative role by indirect inhibitory pathways.
Some AP-1 abundances were obviously suppressed by silencing Nrf2 in Nrf1α−/− cells (Figure 2I), and strikingly prevented by inactive Nrf2−/−ΔTA, by comparison with equivalent controls (Figure S4F). Together with the above-described results, these imply that AP-1 is dominantly repressed by Nrf1α, but positively regulated by Nrf2. Rather, no available evidence has been presented here to support the notion that AP-1 activates transcription of Nrf2 (Tao et al., 2014). In mouse embryonic fibroblasts (MEFs), COX2 is co-regulated by Nrf1 and Nrf2, because its abundance was significantly abolished by global knockout of Nrf1 or Nrf2 (Figure S5C). Here, it should also be noted that global knockout of all mouse Nrf1 or Nrf2 DNA-binding domain-containing fragments was achieved by both gene-targeting manipulations (Ohtsuji et al., 2008; Tsujita et al., 2014). This is totally distinctive from specific gene-editing to delete the designed portions of human Nrf1α or Nrf2 (Figure 1). Importantly, knockout of Keap1 in MEFs (Figure S5D) and human HepG2 (Figure S5E) caused a remarkable increase in expression of Nrf1, Nrf2, COX2, and HO-1 to different extents detected. Overall, the precision regulation of COX2 by Nrf1 and Nrf2, along with Keap1, in distinct manners, is preferable to depend on distinctive cell types in different species.
Nrf1α and Nrf2 transactivate ARE-driven miR-22 signaling to PTEN, but not to COX1
On the contrary to COX2, the isoenzyme COX1 was highly expressed in Nrf2−/−ΔTA cells (Figure 2C), but its expression was almost completely abolished in Nrf1α−/− cells (Figure 2B) and also not rescued by restoration of ectopic Nrf1 into Nrf1α−/− cells (Figure 2F), albeit Nrf2 was up-regulated (Figure 2G). Thereby, it is inferable that no matter how Nrf1α and Nrf2 have opposing or overlapping roles in regulating COX1 expression, Nrf2 exerts a dominant inhibitory effect on COX1, but this effect is fully contrary to regulating COX2. Thus, we speculate that the putative inhibition of COX1 by Nrf2 (and possibly Nrf1α) may be achieved through an indirect miRNA-regulatory pathway, except for directly ARE-binding to this gene. Fortunately, a candidate miR-22 was selected by predicting possibly miRNA-binding sites within the COX1 3′-UTR region (see http://www.targetscan.org/vert_72/). As expected, the real-time qPCR analysis unraveled that miR-22 expression was significantly increased in Nrf1α−/− cells but decreased in Nrf2−/−ΔTA cells (Figure 3A). Forced expression of Nrf1 or Nrf2 also caused an obvious increase in miR-22 expression in wild-type Nrf1/2+/+ cells (Figure 3B). Further analysis of the miR-22-coding gene revealed there exists a consensus ARE site within its promoter (Figure 3C, upper panel). The promoter-driven luciferase reporter (i.e. miR22-ARE-Luc) was created, so as to assay for its transcription activity. The results showed that the miR22-ARE-Luc reporter gene was significantly transactivated by Nrf1 and Nrf2 (Figure 3C), and the transactivation was diminished by the mutant miR22-AREm-luc. Together, these imply direct and indirect transactivation of miR-22 possibly by Nrf1α and Nrf2.
Since negative regulation of PTEN by miR-22 had been reported (Fan et al., 2016; Tan et al., 2012), a Renilla reporter gene containing the 3’UTR region of PTEN (i.e. PTEN-miR22b) was here constructed, together with a mutant of miR-22-binding site (i.e. PTEN-miR22b-mut, Figure 3D, upper panel). If miR-22 would bind the 3’-UTR region of PTEN transcripts, the PTEN-miR22b-driven Renilla activity was significantly reduced by miR22 (Figure 3D, lower panel), and also partially decreased by ectopic expression of Nrf1 or Nrf2 (Figure 3E). These negative effects were sufficiently abrogated by PTEN-miR22b-mut. Consistently, both mRNA and protein levels of PTEN were significantly reduced in Nrf1α−/− cells (with hyper-expression of Nrf2) but strikingly increased in Nrf2−/−ΔTA cells (Figure 3F). Notably, such opposing changes in PTEN levels are inversely correlated with the relevant values of miR22 measured in same cell lines (Figure 3A). Thus, transactivation of miR-22 by Nrf1α and Nrf2 leads to putative inhibition of PTEN.
To further determine whether such miR-22 pathway is involved in the regulation of COX1 by Nrf1 and Nrf2, the luciferase reporter gene was constructed by cloning the 3’-UTR sequence of COX1 (i.e. COX1-miR22b), along with a mutant of the putative miR-22 binding site to yield a COX1-miR22b-mut reporter (Figure 6A, upper panel). However, the COX1-miR22b-driven Renilla activity was unaltered by miR-22, Nrf1 and Nrf2, when compared with that of COX1- miR22b-mut (Figure S6A1, S6A2). Another luciferase reporter gene (i.e. PCOX1-Luc) was engineered by inserting the 1413-bp COX1 gene promoter, but the PCOX1-Luc activity was also unaltered by forced expression of Nrf1 and Nrf2 (Figure 6B1). However, the responsiveness of the PCOX1-Luc to TPA was induced (Figure S6B2), albeit it was relatively weak, when compared to the PCOX2-Luc (Figure S2A). Intriguingly, the PCOX1-Luc activity was modestly mediated by Jun, but almost unaffected by a canonical AP-1 dimer (Figure S6B3). This is consistent with the notion from (Smith et al., 1997), but further insights are required into the mechanisms underlying the regulation of COX1 by Nrf1α and Nrf2.
Nrf1α and Nrf2 have mutual regulatory effects on downstream genes
Since an unusual increase in Nrf2 protein is accompanied by relative higher levels of ROS in Nrf1α−/− cells (Figures 1F, 2G), it is inferable that Nrf1α-deficient hepatoma cells are growing under severe redox stress conditions redefined at a new higher steady-state level leading Nrf2 to become hyperactive. As anticipated, mRNA expression levels of HO-1, GCLC, GCLM, NQO1 and xCT (they are co-target genes mediated by Nrf1 and Nrf2 (Leung et al., 2003; Ohtsuji et al., 2008; Tsujita et al., 2014) were significantly increased Nrf1α−/− cells (Figure 4A). Meanwhile, a marked decrease in LPIN1, but no significant reduction in PGC-1β (both were identified as Nrf1-specific target genes by (Hirotsu et al., 2012)), was determined by comparison with equivalents of wild-type Nrf1/2+/+ cells. Despite no obvious alterations in mRNA levels of Nrf2 (Figure 4A), Western blotting revealed significant increases in the abundance of Nrf2 protein and typical downstream gene products HO-1, GCLM, NQO1 and HIF1α in Nrf1α−/− cells, by contrast with Nrf1/2+/+ cells (Figure 4B). All four protein levels of HO-1, GCLM, NQO1 and HIF1α were, however, markedly reduced in accordance with knockdown of Nrf2, by siRNA-targeting interference with Nrf1α−/− cells (Figure 3C). Silencing of Nrf2 also led to decreased mRNA expression levels of HO-1, GCLM and xCT (Figure S5F). Conversely, restoration of ectopic Nrf1 expression into Nrf1α−/− cells caused obvious decreases in abundances of Nrf2, HO-1, GCLM and NQO1 to different extents as detected (Figure 4D). Collectively, it is demonstrated that in Nrf1α−/− cells, hyper-active Nrf2 has a potent ability to mediate a subset of their co-target genes. Furthermore, the phosphorylated JNK, but not its total, proteins were markedly decreased, as Nrf2 protein was reduced by ectopic expression of Nrf1 after transfecting into Nrf1α−/− cells (Figure 4D). This finding, together with the evidence that Nrf2 is repressed by JNK inhibitor treatment of Nrf1α−/− cells (Figure 2H), implicates that Nrf2 may govern a not-yet-identified upstream kinase to phosphorylate JNK through a positive feedback loop.
By contrast, inactivation of Nrf2 led to strikingly decreases in both mRNA and protein levels of Nrf1 in Nrf2−/−ΔTA cells (Figure 4E, 4F). This was accompanied by significantly diminishments in the expression of their co-regulated downstream genes HO-1, GCLM, NQO1 and HIF1α in Nrf2−/−ΔTA cells (Figure. 4E, 4F), except with a modest reduction in LPIN1 and PGC-1β mRNA levels. Thereby, such marked decreases in expression of Nrf1, HO-1, GCLM, NQO1 and HIF1α resulting from loss of Nrf2 function demonstrate that Nrf2−/−ΔTA cell line could provide a favorite model to determine the changing downstream genes regulated by Nrf1, Nrf2 alone or both. Next, to address this, Nrf2−/−ΔTA cells were allowed for the ectopic expression of Nrf1 or Nrf2 in order to estimate specific downstream genes. As expected, it is validated that Nrf1-specific target gene PSMB6 was increased by forced expression of Nrf1, but not Nrf2 allowed for restoration in Nrf2−/−ΔTA cells (Figure 4G). Conversely, expression of NQO1 was induced by ectopic Nrf2, rather than Nrf1, after being transfected into Nrf2−/−ΔTA cells. This implies that NQO1 is Nrf2-dependent, but insensitive to Nrf1 in Nrf2−/−ΔTA cells. In fact, Nrf1 and Nrf2 have overlapping roles in mediating transactivation of HO-1 and GCLM (Figure 4G, 4H). Intriguingly, both CNC-ZIP factors also enhanced expression of COX2, but reduced COX1 expression (Figure 4G, 4H). This seems consistent with additional examinations, revealing that silencing of Nrf2 in Nrf1α−/− cells gave rise to a relative higher expression of COX1, with an accompanying decrease in COX2 (Figure S5F). Such co-inhibition of COX1 by two transcriptional activators Nrf1 and Nrf2 is puzzling, albeit it is known that transcriptional expression of downstream genes is mediated by their functional heterodimers with a partner of small MAF or other bZIP proteins through directly binding the cis-regulatory ARE sites in their promoters (Yamamoto et al., 2018; Zhang and Xiang, 2016). Together with the above data (Figures 2, 3), these collective findings indicate that Nrf1 and Nrf2 may also be two indirect players in the transcriptional regulation of COX1 by an unidentified pathway.
To determine which specific genes are constitutively activated by Nrf2, a dominant constitutive active mutant caNrf2ΔN-expressing cell line was established by the gene-editing to delete the N-terminal Keap1-binding portion of Nrf1 (Figure S5A). The resulting caNrf2ΔN cells indeed gave rise to a higher expression of Nrf2, as well as Nrf1, when compared to wild-type cells (Figures 4I, S5G). Interestingly, expression of COX1 almost disappeared as accompanied by significant increases of COX2 in caNrf2ΔN cells (Figures 4I, S5G). This further supports the above evidence obtained from inactivation of Nrf1α and Nrf2. Constitutive presence of caNrf2ΔN also led to increases in abundances of both HO-1 and GCLM (Figure 4I), in addition to an enhanced expression of xCT and Lpin1 (Figure S5G). Furthermore, phosphorylated JNK was significantly induced by caNrf2ΔN, with no changes in total JNK protein (Figure 4I), implying there may exist a putative upstream kinase monitored by Nrf2.
To further assess a mutual regulatory relationship between Nrf1 and Nrf2, we herein examined whether one of the endogenous proteins was influenced by another of both proteins that were allowed for ectopic over-expression in wild-type Nrf1/2+/+ cells. As shown in Figure 4J, the endogenous Nrf2 protein was obviously decreased by ectopic Nrf1. Consequently, abundances of HO-1 and GCLM were markedly increased, whereas COX2 was weakly enhanced, but COX1 was significantly decreased following over-expression of Nrf1 (Figure 4J). By contrast, over-expression of ectopic Nrf2 caused an enhancement in endogenous Nrf1 (Figure 4K). This was accompanied by striking increases of COX2, HO-1 and GCLM, along with a remarkable decrease of COX1 (Figure 4K). Altogether, we assume there exists a mutual inter-regulatory relationship between Nrf1α and Nrf2, as summarized in Figure 4L. This may be an important strategy for a precision regulation of distinct downstream genes, to meet the needs for different cell processes.
Nrf1α and Nrf2 transactivate the Nrf1 promoter-driven reporter at different sites
To gain insights into the direct relationship between Nrf1 and Nrf2, we constructed their specific luciferase reporters by cloning the promoter regions of Nrf1 and Nrf2 genes and evaluated their activity by transfection into HepG2 cells (Figure 5A, 5B). As anticipated, the results showed that both PNrf1-luc and PNrf2-luc reporter genes were significantly induced by thapsigargin (TG, a classic ER stressor), or tert-Butylhydroquinone (tBHQ, a typical oxidative inducer), but not vitamin C (VC, a dual redox inducer) (Figure 5C). Thereby, PNrf1-luc and PNrf2-luc reporters are available to assess transcriptional expression of Nrf1 and Nrf2. Subsequently, co-transfection of expression constructs for Nrf1 or Nrf2, together with PNrf1-luc or PNrf2-luc reporters, revealed that the transcription of PNrf1-luc, but not PNrf2-luc, genes was markedly induced by Nrf1 and Nrf2 (Figure 5D). Although no canonical ARE sequence (5′-TGACxxxGC-3′) exist in the 5025-bp Nrf1 gene promoter, an attempt to identify which sites are located in the promoter enabling for specific transactivation by Nrf1 and Nrf2 was made, in order to yield a series of truncated mutants from PNrf1-luc (Figures 5A). Fortunately, the resulting luciferase assays uncovered that several reporters containing the first exon region of Nrf1 were activated by Nrf1 and Nrf2 possibly through different regulatory sites (Figure 5B). From various lengths of the PNrf1-luc and mutants, it is inferable that the Nrf1/Nfel1-regulatory locus site-1 (i.e. Site-1) specific for Nrf2 is located in a 62-bp range between +572 bp and +634 bp, and the Nrf1/Nfel1-regulatory locus site-2 (i.e. Site-2) specific for Nrf1 per se is situated in another 100-bp range from +1031bp to +1131bp (Figure S7A).
Nrf1α−/−-leading accumulation of Nrf2 results from decreased Keap1
The putative inter-regulation between Nrf1α and Nrf2 was further investigated to interpret the rationale underlying an abnormal accumulation of Nrf2 protein with no changes in its mRNA expression in Nrf1α−/− cells (Figure 2G,4A). Based on this finding, combined with the nation that Nrf1, but not Nrf2, acts as a primary transcriptional regulator of 26S proteasomal subunits (Radhakrishnan et al., 2010; Steffen et al., 2010), thereby it is hypothesized that aberrant accumulation of Nrf2 results from loss of Nrf1α’s function leading to an imbalance between Nrf2 protein synthesis and degradation processing. As shown in Figure S7(B, C), total protein ubiquitination was significantly accumulated in Nrf1α−/− cells, but not in Nrf2−/−ΔTA cells, when compared with wild-type cells. Further analysis of mRNA expression levels revealed that 20 of 36 genes encoding all 26S proteasomal subunits and relevant proteins were significantly reduced by knockout of Nrf1α (with only an exception of PSMB10 enhanced) (Figure S7D). By contrast, no marked changes in transcriptional expression of 31 of the above 36 genes (except that PSMB3, PSMB10, PSMC5, and PSMD3 were reduced and PSME1 increased) were determined in Nrf2−/−ΔTA cells (Figure S7E). Therefore, such proteasomal dysfunction by loss of Nrf1α may result in an accumulation of Nrf2 by impaired proteasomal degradation pathway.
To address this, Nrf2 protein turnover was further determined by pulse-chase analysis of its half-life in Nrf1α−/− cells (Figure 5E). Surprisingly, it was found that Nrf1α−/− cells gave rise to relatively stable protein of Nrf2 with a prolonged half-life to 2.71 h (=163 min) after treatment with cycloheximide (CHX, an inhibitor of newly-synthesized polypeptides), and also such longevity of Nrf2 was largely unaffected by the proteasome inhibitor MG132 (Figure 5F, lower panel). As controls, Nrf1+/+ cells displayed rapid turnover of Nrf2 with a short half-life of 0.38 h (=23 min) after CHX treatment, and this lifetime was extended to 1.17 h (= 70 min) by MG132 (Figure 5F, upper panel). Overall, the aberrant accumulation of Nrf2 in Nrf1α−/− cells results from impaired proteasome-mediated degradation.
Next, several upstream regulators of Nrf2 were examined to determine which pathways are impaired towards its protein turnover in Nrf1α−/− cells. Intriguingly, an abundance of Keap1 protein was significantly decreased (Figure 5H), even though its mRNA expression levels were unaltered, along with its turnover regulator p62 was strikingly reduced in Nrf1α−/− cells (Figure 5G). Thereby, turnover of Keap1 may also occur through a p62-independent pathway. As such, impairment of Keap1-mediated proteasomal degradation of Nrf2, in particular, oxidative stress (Kobayashi et al., 2006), is likely to contribute to an aberrant accumulation of Nrf2 by the loss of Nrf1α. However, accumulation of Nrf2 is attributable to another impairment of GSK3β-phosphorylated β-TrCP-mediated proteasomal degradation of the CNC-bZIP protein. This is due to a marked decrease of GSK3β at mRNA and protein levels in Nrf1α−/− cells (Figure 5G,5H).
Nrf1α and Nrf2 exert opposing and unifying roles in the regulation of PTEN signaling
More importantly, we found that both protein and mRNA levels of PTEN (acts as a key master versatile regulator of Nrf2, Keap1, PI3-kinase, AKT and GSK3β (Pitha-Rowe et al., 2009; Rojo et al., 2014; Sakamoto et al., 2009; Taguchi et al., 2014), were significantly diminished or even abolished in Nrf1α−/− cells (retaining high expression of Nrf2) (Figure 5I, left panel). In contrast, inactivation of Nrf2 caused a striking increase in PTEN mRNA, but not its protein levels, in Nrf2−/−ΔTA cells (yielding low expression of Nrf1) (Figure 3F, 4F). On the contrary, in caNrf2ΔN cells (giving rise to a high expression of Nrf2 and Nrf1, Figure 4I), a significant decrease in PTEN protein abundance, but not its mRNA levels, was determined (Figure 5I). Collectively, together with the above-described data (Figure 3), both Nrf1α and Nrf2 are much likely to exert opposing and unifying roles in the precision regulation of PTEN by both miR-22-dependent and -independent pathways, in which Nrf2 is preferably dominant-negative, whereas Nrf1α has a limited positive role.
Further analysis of the PTEN gene unraveled that there exist two typical ARE sites within its promoter region (Figure 3G). The luciferase assays demonstrated that transcription activity of the PTEN promoter-driven luciferase reporter PPTEN-luc was significantly induced by Nrf1, but not by Nrf2 (Figure 3H). Mutagenesis analysis uncovered that the second ARE2 site made a primary contribution to transactivation activity of the PPTEN-luc reporter by Nrf1, while the first ARE1 site also gained a minor contribution to Nrf1-mediated transactivation of PPTEN-luc (Figure 3I).
Based on the fact that loss of PTEN function leads to constitutive activation of the PI3K-AKT signaling pathway to augment the nuclear accumulation of Nrf2 and its resulting activation (Mitsuishi et al., 2012; Sakamoto et al., 2009), we determined whether the PI3K-AKT signaling is activated by abolishment of PTEN in Nrf1α−/− cells (in which Nrf2 is aberrantly accumulated). The results demonstrated Nrf1α−/−-leading increased abundances of Nrf2, AKT1, COX2 and HO-1, but such increases were significantly suppressed by the classic mTOR inhibitor, rapamycin (RAPA) (Figure 5J). This implies that the mTOR may also be activated in Nrf1α−/−cells. Accordingly, increased abundances of both AKT and phospho-S6K1 in Nrf1α−/− cells were markedly blocked by mTOR inhibitor RAPA. This is inversely correlative with the consequence that over-expression of Nrf1 suppresses AKT induction (Hirotsu et al., 2014). Together, this study indicates opposing and unifying cross-talks between Nrf1α and Nrf2 to regulate the PTEN-mTOR-AKT signaling to the Nrf2-COX2 pathway. Based on these findings, we summarized an endogenous inter-regulatory network (Figure 5K).
Blockage of Nrf1α +/+-bearing or Nrf1α−/−-derived tumor growth by Nrf2 deficiency
Our previous work revealed that malignant growth of Nrf1α−/−-derived hepatoma is accompanied by metastasis to the liver in xenograft mice (Ren et al., 2016). Here, to elucidate what effects have been elicited by Nrf1α and Nrf2 on tumor repression or promotion, we further investigate distinct genotypic tumors derived from Nrf1/2+/+, Nrf1α−/−, Nrf1α−/−+siNrf2, Nrf2−/−ΔTA and caNrf2ΔN cells in xenograft mice. Their tumorigenicity was evaluated by measuring tumor volume and weight. As illustrated in Figure 6(A to C), Nrf2−/−ΔTA cells were inoculated in nude mice, but did not form more than one solid tumor. This implies that tumorigenicity of Nrf1/2+/+ cells, as controls, is almost completely abolished by inactivation of Nrf2. Conversely, constitutive activation of Nrf2 did not obviously influence the resulting caNrf2ΔN-driven tumorigenicity, by comparison to that of Nrf1/2+/+. This indicates that Nrf2-prone cancer promotion is dominantly confined by the presence of Nrf1α. Upon loss of Nrf1α function in Nrf1α−/− cells (in which hyper-active Nrf2 is accumulated), the resultant tumorigenicity was hence significantly higher than that of Nrf1/2+/+-tumor, but rather was much strikingly suppressed by silencing of Nrf2 (in the Nrf1α−/−+siNrf2-derived tumors) to the much less extent than that of Nrf1/2+/+ cells (Figure 6, A to C). Collectively, these findings demonstrate that Nrf2 acts as a tumor promoter, but it is efficiently confined by Nrf1α serving as a dominant tumor repressor, implying both are a pair of mutual antagonizing twin factors. Overall, malignant transformation of Nrf1α−/−-derived cells is attributable to hyperactivation of Nrf2.
Histological examination showed that a considerable number of blood vessels were formed in Nrf1α−/− tumors but was reduced by Nrf2 knockdown in Nrf1α−/−+siNrf2-derived tumors (Figure 6D). However, no marked differences in vascularity between caNrf2ΔN-and Nrf1/2+/+-bearing tumors were observed. Further insights into angiogenesis-related genes revealed that mRNA expression levels of VEGFA, VEGFC, VEGFD, EGFR, but not HIF1α or STAT1 were strikingly elevated by knockout of Nrf1α, but the increased expression of VEGFC, VEGFD and EGFR was significantly reduced by silencing Nrf2 (Figure 6E). Notably, knockdown of Nrf2 almost completely abolished expression of HIF1α and STAT1 in Nrf1α−/−+siNrf2 cells, but no changes in these two factors were observed in Nrf1α−/− cells, as compared to those obtained from Nrf1/2+/+ cells. Rather, all the other angiogenesis genes except VEGFD were up-regulated in caNrf2ΔN cells (giving high expression of Nrf1 and Nrf2), while only STAT1 but not other genes were up-regulated by inactive Nrf2−/−ΔTA (Figure 6E). Altogether, both Nrf1α and Nrf2 are diversely involved in regulating the expression of angiogenesis genes except for STAT3 as examined above.
Intriguingly, the vascularity of Nrf1α−/−+siNrf2-derived tumors seemed to be higher than that Nrf1/2+/+-bearing tumors (Figure 6D), but, such angiogenetic changes cannot explain the observation that the Nrf1α−/−+siNrf2-tumor volumes and weights were significantly less than those obtained from the Nrf1/2+/+-tumors. This implicates other rationales beyond angiogenesis. Thus, we employed flow cytometry to determine changes in the cell cycle and apoptosis in five distinct cell lines. As shown in Figure 6(F, G), the S-phase of Nrf1α−/−+siNrf2 cells was significantly shortened. Such a severe S-phase arrest of cell cycle is supported by quantitative gene expression analysis revealing that significant up-regulation of p16, p19, p21 p53 and CDK4 was simultaneously accompanied by down-regulation of RB1, CDK1, CyclinA2, CyclinB2, E2F3, E2F5, and E2F6 in Nrf1α−/−+siNrf2 cells, when compared with its progenitor Nrf1/2+/+ or Nrf1α−/− cells (Figure S8A). In addition to the S-phase arrest, the G0/G1-phase was relatively extended in Nrf1α−/−+siNrf2 cell cycle (Figure 6G). Consistently, apoptosis of Nrf1α−/−+siNrf2 cells was also significantly enhanced, when compared to other cell lines (Figure 6H, S8D). This is also supported by further analysis of apoptosis-related genes unraveling that Bax, Bak, Bid, Bad, and Puma were significantly up-regulated, while anti-apoptotic BCL-2 gene was down-regulated, with no changes in BCL-xL and Mcl-1 in Nrf1α−/−+siNrf2 cells (Figure 6I).
Although no significant differences in growth and vascularity of between caNrf2ΔN-and Nrf1/2+/+-bearing tumors, the G2/M-phase of the caNrf2ΔN cell cycle was shortened, along with the S-phase extended (Figure 6G). This implies that a G2/M-phase arrest is likely caused by the constitutive activation of Nrf2, in agreement with the supportive evidence that inactivation of Nrf2 markedly prolonged the G2/M-phase of Nrf2−/−ΔTA cells (Figure 6G). Further gene expression analysis revealed that p15, p21 and Puma were significantly up-regulated, but p18, CDK1, E2F2 and Bid were down-regulated by caNrf2ΔN (Figure 6I, S8A). Conversely, inactive Nrf2−/−ΔTA still up-regulated RB1, CDK1, E2F3, and Cyclin D1 (Figure S8A), but strikingly down-regulated FTH1 and FTL (both encode ferritin heavy and light chains involved in iron-dependent lipid peroxidation and ferroptosis, in Figure S8G). Overall, these demonstrate that Nrf1α and Nrf2 coordinately regulate certain key genes involved in cell cycle and apoptosis.
SEM (n=3, *p< 0.01, ** p< 0.001; $, p< 0.01; $$, p< 0.001).
Different subsets of genes are finely regulated by Nrf1α, Nrf2 alone or both
Nrf1 and Nrf2 are two important CNC-bZIP transcription factors that are widely expressed in various tissues and also regulate seemingly similar expression patterns of ARE-driven downstream genes that have been identified (Bugno et al., 2015; Tebay et al., 2015). In fact, the ever-accumulating evidence demonstrates that Nrf1 and Nrf2 exert many different and even opposing functions and in particular, unique indispensable functions of Nrf1 are not substituted by Nrf2 (Zhang and Xiang, 2016). Accordingly, the above-described data also unraveled that both CNC-bZIP factors have elicited mutual synergistic and antagonistic roles in regulating precision expression of cognate genes in distinct cell processes, aiming to maintain normal cellular homeostasis. Here, to further evaluate the functional similarities and differences between Nrf1α and Nrf2, the genome-wide expression of genes in Nrf1/2+/+, Nrf1α−/−, Nrf1α−/−+ siNrf2, Nrf2−/−ΔTA and caNrf2ΔN cells was determined by transcriptome sequencing. Those detectable genes with a fold change ≥ 2 and diverge probability ≥ 0.8 were defined as differentially expressed genes (DEGs), by comparison with equivalents measured from Nrf1/2+/+ cells (Figure 7A). Consequently, Nrf1α−/− cells gave rise to 1,213 of DEGs (i.e. 697 up-plus 850 down-regulated), but the number of DEGs in Nrf1α−/−+siNrf2 cells was significantly increased to 3,097 genes, 2247 of which were down-regulated by siNrf2. Intriguingly, only 545 of DEGs were detected in Nrf2−/−ΔTA cells, implying that many genes are silenced or prevented by inactive Nrf2 mutant (distinctive from simple knockout of this factor). These data suggest that, in this regulatory system by the cooperation of Nrf1 and Nrf2, a single change of both has only limited effects on overall gene expression, and thus both changes will have a greater impact. For instance, when compared to those of Nrf1α−/− cells, silencing of Nrf2 caused 124 genes to be up-regulated, and still led 1,338 genes to be down-regulated in Nrf1α−/−+siNrf2 cells (Figure 7A, last column), so that malignant growth of Nrf1α−/−-derived tumor was repressed by Nrf2 knockdown. Conversely, reinforced expression of Nrf2 (and Nrf1) in caNrf2ΔN cells up-regulated 1655 genes and also down-regulated 423 genes. These findings indicate that Nrf2 is a dominant activator to regulate many genes, while Nrf1α appears to exert dominant negative effects on some genes.
Enrichment analysis revealed that DEGs of Nrf1α−/− cells were subject to 16 pathways (p < 0.001), of which 9 are responsible for human disease and 4 are involved in the environmental information processing (Table S1). By contrast, most of the cellular processes were significantly changed in Nrf2−/−ΔTA and Nrf1α−/−+siNrf2 cells. Thus, loss of Nrf1α relevant to the disease suggests that its function is essential for maintaining cellular homeostasis, while Nrf2 exerts its greater roles in regulating most of cellular physiological processes. For example, the above-described alterations in the cells cycle of Nrf1α−/−+siNrf2 were also validated by transcriptome (Table S1). Further calculation of the DEGs distribution unraveled that signal transduction, cancer-relevant, immune system and metabolism were most abundant secondary KEGG pathways in Nrf1-or Nrf2-deficient cells (Figure 7B). An insight into the cellular signaling transduction uncovered that the most DEGs are involved in the PI3K-AKT pathway (Table S1). In this pathway, a key tumor suppressor PTEN was significantly and oppositely altered in both Nrf1α−/− and Nrf2−/−ΔTA cell lines (Figures 3F, 7C, 7D). Based on these specific findings, much-focused DEGs in Nrf1α−/− and Nrf2−/−ΔTA cells were mapped according to the KEGG pathway. The results illustrated that both cell lines displayed such significant opposing changes in the PI3K-AKT pathways (Figures 7C, 7D, S9A). As interested, knockout of Nrf1α (with accumulated Nrf2) caused a general reduction in transcription of most AKT-signaling molecules, but they were hence generally increased by inactivation of Nrf2. Such striking disparity is dictated by the distinction of Nrf2 proteins in between the two cell lines (Figure 2).
Notably, albeit seemingly similar downstream genes are regulated by Nrf1 and Nrf2, de facto activation of Nrf2 by knockout of Nrf1α can inevitably cause their opposite effects on some genes against theoretic expectations. This is further evidenced by results from Nrf1α−/−+siNrf2 cells, revealing that many of those accumulated Nrf2’s effects on downstream genes by Nrf1α−/− were strikingly reduced by knockdown of Nrf2. Therefore, by comparison of the DEGs between Nrf1α−/− and Nrf1α−/−+siNrf2 cell lines, an opposite expression profiling of 87 genes was uncovered by Nrf2 knockdown (Figure S9B-D). About 24 % of these genes are responsible for metabolism-related enzymes. This implies that the function of Nrf2 is closely related to cellular metabolism, particularly in the absence of Nrf1α. This is further approved by another opposite expression profiling of other 83 DEGs in between Nrf2−/−ΔTA and caNrf2ΔN cell lines (Figure S10). Still 16% of the differential expression genes are related to metabolism process, but 24% of these genes are involved in signaling transduction. This observation indicates that in the presence of Nrf1α, Nrf2 is a major player in cellular signaling cascades, but its role in metabolism appears to be restricted possibly by Nrf1α.
The Venn diagrams illustrated that distinct subsets of DEGs were regulated by Nrf1, Nrf2 alone or both (Figure 7E). The common genes regulated by Nrf1α and Nrf2 were seen by comparison of DEGs in Nrf1α−/− or caNrf2ΔN with wild-type. In the intersection of Nrf1α−/− and caNrf2ΔN, the remaining portions after excluding Nrf1α−/−+siNrf2 with Nrf1α−/− were composed of the (red numbered) genes closely correlated to regulation by Nrf1α. The genes regulated by Nrf2 were also found by comparison of DEGs in Nrf1α−/−+siNrf2 with Nrf1α−/−, as well as Nrf2−/−ΔTA or caNrf2ΔN with wild-type, so the intersection of these three sets comprised the (blue numbered) genes preferably regulated by Nrf2. Further, based on the changes in Nrf1 and Nrf2 proteins detected in distinct cell lines (Figure 7F), we screened which portions of high-relevant downstream genes were consistent with or opposite to the changing trends of Nrf1 or Nrf2, respectively. Consequently, 30 Nrf1α-specific downstream genes were shown (in Figure 7G, left panel), of which 17 genes were up-regulated and 13 genes were down-regulated. Meanwhile, 38 Nrf2-specific downstream genes were also found herein, of which 25 were up-regulated and 13 were down-regulated (right panel). Collectively, our findings provide an axiomatic rationale for differential expression of different subsets of genes to dictate distinct phenotypes of animal xenograft tumors (Figure 7H). Significantly, the malfunction of Nrf2 is as a potent tumor promoter, but it can be efficiently confined or suppressed by Nrf1α acting as a dominant tumor repressor.
DISCUSSION
Accumulating evidence has demonstrated that Nrf1 is a key player in the pathogenesis of NASH and HCC, as well as other relevant cardiovascular diseases and type 2 diabetes (Bugno et al., 2015; Zhang and Xiang, 2016). However, it should be noted that these experimental mouse genomes were manipulated to delete all Nrf1 isoforms from the single Nrf1/Nef2l1 gene. In this study, human Nrf1α-specific knockout was achieved by the gene-editing to create the frameshift mutation. The phenotypes of NASH and malignancies were reconstructed by using monoclonal Nrf1α−/− cell lines. Thereby, this provides an available model for a follow-up study to elucidate the relevance of Nrf1α with NASH and its malignance into HCC. In the Nrf1α−/−-leading model, the inflammation marker COX2 is constitutively increased, which entails a non-resolving feature. By contrast, the development-related COX1 was almost completely abolished in Nrf1α−/− cells. The resultant metabolites of arachidonic acid by the rate-limiting enzyme COX2, which also serves as a direct target of Nrf2 (Itoh et al., 2004; Sherratt et al., 2003), are much likely to play a crucial role in the development and progression of inflammation, particularly NASH and hepatoma caused by knockout of Nrf1α.
Further examinations revealed that the Nrf1α−/−-caused increase of COX2 occurred by accumulated Nrf2 protein, but both were effectively diminished by inhibitors of JNK (i.e. SP600125) and mTOR (i.e. rapamycin). Hence, the Nrf2-COX2 pathway is inferable to be regulated by both JNK and mTOR signaling, albeit the detailed mechanisms remain unclear. Here, we found that inhibition of the Nrf2-COX2 pathway is accompanied by decreases in AKT, S6K1 and GSK3β. This is consistent with the claim that Nrf2 is regulated by the mTOR-AKT-GSK3β pathway (Yang et al., 2018). Our findings also unravel that Nrf2 may be monitored by JNK signaling towards AP-1 pathway, but in turn, some AP-1 components (i.e. Jun, Fra-1) are mediated by Nrf2 insofar as to form a feedback loop. Contrary to Nrf1α−/−, MEFs of Nrf1−/−(ΔDBD), in which almost all DBD (DNA-binding domain)-containing Nrf1 isoforms are disrupted (Hirotsu et al., 2012; Ohtsuji et al., 2008; Tsujita et al., 2014; Xu et al., 2005), exhibited marked decreases in total COX2 and most of Nrf2 to much lower levels roughly similar to those determined in Nrf2−/−(ΔDBD) MEFs. (Figure S5C). This difference between human Nrf1α−/− and mouse Nrf1−/−(ΔDBD) demonstrates Nrf1 isoform-dependent regulation of the Nrf2-COX2 pathway in distinct species as experimented.
Notably, an accumulation of free radicals in Nrf1−/−(ΔDBD) MEFs results from decreased expression of ARE-driven genes involved in glutathione synthesis, antioxidant and detoxification (Kwong et al., 1999). Similar but different stress caused by liver-specific knockout of Nrf1−/−(ΔDBD) activates a subset of Nrf2-dependent ARE-battery genes in mice, but Nrf2 cannot still compensate for the loss of Nrf1’s function leading to NASH and HCC (Ohtsuji et al., 2008; Xu et al., 2005). The inducible liver-specific knockout of Nrf1−/−(ΔDBD) in mice increased glutathione levels; this results from up-regulation of xCT (a component of the cystine/glutamate antiporter system XC-), but with no changes in glutathione biosynthesis enzymes (Tsujita et al., 2014). In this work, human Nrf1α−/− increases ROS and lipid levels, along with high expression of xCT and other ARE-driven genes (e.g. HO-1, GCLC, GCLM, NQO1). These genes are Nrf2-dependent because their expression is reduced by inactive Nrf2−/−ΔTA mutant and also repressed by silencing of Nrf2 (in Nrf1α−/− +siNrf2 cells). In addition to COX1 and COX2, both Alox5 and FLAP (also involved in arachidonic acid metabolism) are significantly up-regulated in Nrf1α−/− cells, and also modestly increased in Nrf2−/−ΔTA cells. However, liver-specific Nrf1−/−(ΔDBD) mice display no changes in COX1, COX2 and Alox5 expression (Tsujita et al., 2014). Overall, these discrepancies are likely attributed to the variations of which Nrf1 isoforms have two-sided effects on Nrf2 and diverse downstream genes, depending on different cell types in distinct species. Hence, it is crucially important to determine the bona fide effects of Nrf1 and Nrf2 alone or in combination on distinct cognate genes within regulatory networks (Figure 5K).
Albeit Nrf1 and Nrf2 are recruited for directly binding the ARE sites in the COX1 and COX2 promoter regions (Itoh et al., 2004; Sherratt et al., 2003), our evidence unravels that both CNC-bZIP factors have different or opposing roles in bi-directional regulation of COX1 and COX2 by distinct interrelated positive and negative pathways. In particular, Nrf1α has a two-handed potency to execute as an activator or repressor, depending on distinct cognate genes (e.g. COX1 and COX2), through different regulatory pathways. For example, regulation of COX2 is contributed positively by Nrf2 and negatively by Nrf1α, albeit its promoter-driven PCOX2-Luc reporter is also transactivated by Nrf1 and Nrf2. The direct activation by Nrf1 (as well as Nrf2) may be neutralized or counteracted by its dominant-negative effects triggered by indirect mechanisms (as shown in Figure 5K).
Just contrary to COX2, expression of COX1 is regulated positively by Nrf1α but negatively by Nrf2, albeit no direct activation of its promoter-driven PCOX1-Luc reporter by ectopic Nrf1 and Nrf2 was detected herein. In an attempt to explore into the mechanisms by which COX1 is indirectly regulated by Nrf1/2, we found that both CNC-bZIP factors can directly activate the expression of miR-22 driven by its ARE site. The miR-22, along with Nrf1 and Nrf2, all inhibit the PTEN-miR22b-Renilla reporter activity, implying that these two factors have an intrinsic ability to suppress the tumor suppressor PTEN through activating miR-22, as consistent with the previous reports (Tan et al., 2012; Xu et al., 2012). However, de facto endogenous expression of PTEN at mRNA and protein levels is almost completely abolished in Nrf1α−/− cells (retaining hyper-active Nrf2), but also dramatically increased in Nrf2−/−ΔTA cells (with decreased Nrf1). Collectively, these findings demonstrate that Nrf2 is a dominant negative to inhibit PTEN; this is further evidenced by a significant reduction of PTEN by a priori constitutive activation of Nrf2 in caNrf2ΔNcells (also with enhanced Nrf1). By contrast, Nrf1α has Ying-Yang two-sided effects on PTEN. On one side, Nrf1α acts as a major positive regulator of PTEN, while on the other side of Nrf1α, it is enabled to exert a minor negative role in PTEN, but this negation could be concealed by dominant negative Nrf2 or counteracted by the major positive action of Nrf1α per se.
Since PTEN is known to act as the most critical inhibitor of the PI3K-AKT pathway (Tan et al., 2012; Xu et al., 2012), thereby, inactivation of PTEN by ROS provokes activation of its downstream PI3K-AKT signaling cascades to promote cell survival (Chetram et al., 2011; Kitagishi and Matsuda, 2013). Notably, the ever-increasing evidence demonstrates that PTEN can direct inhibition of expression of ARE-driven gene by inhibiting Nrf2 (Rojo et al., 2014; Sakamoto et al., 2009). Taken together with our results from this study, it is demonstrated that the cellular ROS levels are monitored by Nrf1α-and/or Nrf2-mediating ARE-battery genes, but in turn, expression of Nrf1/2-target genes is also negatively regulated by ROS-activated mir22-PTEN signaling to form a feedback regulatory circuit. Of note, activation of Nrf1/2 by ROS can promote miR-22 expression, which may serve as an important approach to regulate the PTEN-PI3K-AKT pathway. Thereby, the quantitative regulations of cellular ROS levels are achieved by close cooperation of Nrf1α and Nrf2 coordinately through direct and indirect mechanisms, so as to maintain normal redox homeostasis. Conversely, dysfunction of Nrf1α and Nrf2 (particularly its malfunction) leads to severe redox stress and cancer development possibly by the aberrant PTEN-PI3K-AKT signaling pathway.
It is inferable that almost abolishment of PTEN in malignantly growing Nrf1α−/−-derived tumor cells results from an aberrant accumulation of Nrf2 protein, because rescue of PTEN expression occurs after Nrf2 is silenced, such that the existing Nrf1α−/−+siNrf2-derived tumor growth is dramatically repressed by knockdown of Nrf2. In turn, the aberrant accumulation of Nrf2 in Nrf1α−/−cells is caused by impaired PTEN expression. This is fully consistent with the pathology of PTEN−/−-leading cancer, in which the abnormal nuclear accumulation of Nrf2 is caused by impairment of GSK3β-directed β-TrCP-based proteasome-mediated degradation, as described by (Best et al., 2018; Rojo et al., 2014; Taguchi et al., 2014). In addition to impairment of the GSK3β-directed β-TrCP pathway, aberrant accumulation of Nrf2 is augmented by inhibition of Keap1-based proteasome-mediated degradation in Nrf1α−/−-derived tumor cells. Noticeably, the Keap1 protein, rather than mRNA, levels are significantly reduced in Nrf1α−/− cells, albeit its binding partner p62, acting as a major regulator of Keap1 to the autophagic degradation (Kageyama et al., 2018), is strikingly down-regulated in Nrf1α−/− cells. Thus, we postulate that a p62-independent mechanism may account for the Keap1 protein degradation and also is reinforced in Nrf1α−/− cells. Yet, it cannot be ruled out that biosynthesis of Keap1 polypeptides may also be retarded during these conditions.
Several lines of evidence presented here demonstrate that Nrf2 is predominantly negatively regulated by Nrf1α because Nrf1α−/− enables Nrf2 to be released from the confinements by the PTEN-GSK3β-directed β-TrCP-based and Keap1-based proteasomal pathways (Figure 5K). Consequently, accumulation of Nrf2 leads to aberrant activation of ARE-driven cytoprotective genes (e.g. HO-1, GCLM, NQO1) to shelter or promote Nrf1α−/−-driven tumor cells. In fact, These ARE-battery genes can be directly activated by Nrf1α, but some of these downstream genes could also be inhibited through braking control of the Nrf2 activity. Overall, distinct levels of Nrf1 alone or in cooperation with Nrf2 finely tune and also quantitatively regulate expression of diverse downstream genes to meet different cellular needs (Figures 4L, 5K). Thus, these resulting collective effects determine distinct phenotypes of animal xenograft tumor models as deciphered in this study (Figure 7H). Consistently, the malignant growth of Nrf1α−/−-derived tumor is substantially suppressed by knockdown of Nrf2, by comparison with Nrf1α−/−+siNrf2-derived tumor. Conversely, almost no solid tumor is formed in nude mice that have been inoculated by injecting inactive Nrf2−/−ΔTA-derived cells, albeit Nrf1 is slightly decreased with loss of Nrf2’s function. These demonstrate that Nrf1α acts as a dominant tumor suppressor principally by confining the oncogenicity of Nrf2. In turn, Nrf2 exerts a dominant tumor-promoting role in tumorigenesis and malignant growth, but it can also directly mediate the Nrf1 gene transcription to form a feedback regulatory loop. This is validated by further evidence revealing that, upon the presence of Nrf1 in caNrf2ΔN-derived tumor cells, its growth is almost unaffected by constitutive activation of Nrf2, as well as antioxidant and detoxifying genes, when compared with wild-type Nrf1/2+/+-bearing tumor.
In an attempt to clarify those seemingly contradictory results obtained from loss of Nrf1α and its functional gain (i.e. ectopic over-expression), we have surprisingly found that there exists a mutual regulatory relationship between Nrf1α and Nrf2, thereby enabling both factors to elicit opposing and unifying roles in regulating distinct downstream genes (particularly ARE-driven cognate genes). Importantly, we have also discovered that that forced expression of Nrf1 enables the Nrf2 protein to be reduced, whereas loss of Nrf1α led to a significant increase in Nrf2 protein, but not its mRNA levels (Figure 4L). By contrast, both mRNA and protein levels of Nrf1 are increased by over-expression of Nrf2 or its constitutive activation, but also repressed by inactivation of Nrf2. Further experiments have unraveled no activation of the human Nrf2 promoter-driven PNrf2-Luc reporter by Nrf1 or Nrf2, albeit mouse Nrf2 contains ARE sites as described (Kwak et al., 2002). However, the human Nrf1 promoter-driven PNrf1-luc reporter is trans-activated by Nrf1 (at the locus Site-2) and Nrf2 (at the locus Site-1) (Figures 5, S6A). These findings demonstrate there are two (i.e. transcript and protein abundance) levels at which Nrf1α and Nrf2 have cross-talks with each other to influence the expression of ARE-driven genes. Thereby, synergistic or antagonistic effects of Nrf1α and Nrf2 depend on mutual competition or somehow coordination with spatiotemporally binding to the same or different ARE enhancers within downstream genes. Overall, such inter-regulatory cross-talks between Nrf1α and Nrf2 could be a vitally important strategy for the precision regulation of distinct downstream genes. This rationale provides a better explanation of those complicated physio-pathological functions with distinct disease phenotypes exhibited in different models (as reviewed by Menegon et al., 2016; Zhang and Xiang, 2016).
Importantly, a hot controversy surrounds the roles of Nrf2 in the pro-or anti-cancer contexts, termed ‘the Nrf2 paradox’ (Menegon et al., 2016; Rojo de la Vega et al., 2018). This study has defined that function of Nrf2 is dictated by activation or inactivation of Nrf1α. This is because deterioration of Nrf1α−/−-tumor results from hyper-active Nrf2, along with decreased PTEN and activation of AKT signaling, but Nrf1/2+/+-tumor growth is unaffected by constitutive activation of Nrf2 when compared with caNrf2ΔN-tumor. Consistently, it has been recently showed that Nrf2 acts as a tumor-promoting player, depending upon aberrant activation of the PI3K-AKT signaling pathway, whereas it serves as a tumor-preventing player through activating ARE-driven cytoprotective genes under normal activation conditions (Best et al., 2018). However, a similar subset of ARE-driven genes is also highly expressed in Nrf1α−/− and caNrf2ΔN cell lines. Our findings demonstrate that the tumor-promoting role of Nrf2 is determined by loss of Nrf1α function, independent of those cytoprotective gene expressions. Even as a braking control of Nrf2 activity, Nrf1α may play a role for ‘decision-maker’ or ‘executor’ in the cell senescence and cancer progression, since a secretory phenotype of senescent cells occurs by a Nrf2-independent mechanism (Wang et al., 2017), albeit the relevance to Nrf1 needs to be verified.
In conclusion, this study provides a panoramic view of mutual inter-regulatory cross-talks existing between Nrf1α and Nrf2 to determine quantitative expression of distinct downstream genes involved in different patho-physiological processes. Significantly, the axiomatic rationale underlying distinct animal xenograft tumor phenotypes has been also unraveled by transcriptome analysis of the genome-wide gene expression in Nrf1α−/−, Nrf1α−/−+siNrf2, Nrf2−/−ΔTA and caNrf2ΔN cell lines, by comparison with wild-type Nrf1/2+/+. Notably, an overwhelming majority of the PTEN-directed PI3K-AKT signaling cascades are strikingly activated in Nrf1α−/−, but rather repressed in Nrf2−/−ΔTA cells. Silencing Nrf2 leads to opposing expression of 87 genes in between Nrf1α−/− and Nrf1α−/−+siNrf2 cell lines. Although most cognate genes are, to different extents, co-regulated by Nrf1α and Nrf2, this study has highlighted about 30 of Nrf1α-specific downstream genes, and 38 of Nrf2-specific downstream genes. Among Nrf1α-regulated genes, those encoding A2M, EPHA8, FBXO2, KCND1, SLC2A3, SORL1, OLIG2, and RAPGEF4 may be responsible for the nervous system, albeit it is unclear whether they are relevant to those phenotypes of Nrf1α−/−-leading neurodegenerative diseases as reported by (Kobayashi et al., 2011; Lee et al., 2011). Only ACSS2, FA2H, and KLF15 genes are associated with lipid metabolism, but it is required to determine their roles in relevant phenotypes, as described by (Bartelt et al., 2018; Hirotsu et al., 2014; Hou et al., 2018; Xu et al., 2005). By contrast, a portion of Nrf2-specific genes are critical for the development of various tissues and organs, neurons and cardiomyocytes, but none of the specific physio-pathological phenotypes in the Nrf2−/−ΔDBD mice are observed, implying their functions can be compensated. As such, the other Nrf2-specific genes may be involved in the development, movement and adhesion of epithelial cells, but it is unknown whether these gene functions enable Nrf2 to be endowed with its potent tumor-promoting roles in cancer progression and metastasis. All together, the malfunction of Nrf2, as a tumor promoter, is predominantly suppressed by Nrf1α that acts as a dominant tumor repressor. This pathophysiological process is tightly governed by endogenous regulatory networks. On the inside, there exist mutual opposing and unifying cross-talks between Nrf1α and Nrf2 at distinct levels. Concordantly, Nrf2 directly mediates transcription of the Nrf1 gene to form a coupled positive and negative feedback circuit, in order to monitor Nrf1 and Nrf2 functioning towards precision expression of distinct downstream genes.
STAR* METHODS
Detailed methods are provided in the online version of this paper and include the following:
KEY RESOURCES TABLE
CONTACT FOR REAGENT AND RESOURCE SHARING
EXPERIMENTAL MODEL AND SUBJECT DETAILS
Animal care and use
mouse embryonic fibroblasts (MEFs)
Human liver cell lines with distinct genotypes
METHODS DETAILS
Cell culture and transfection
Expression constructs and other oligos used for siRNA and MirRNA
Subcutaneous tumor xenografts in nude mice
Histology
Lipid staining
Cellular ROS staining
Luciferase reporter assay
Real-time quantitative PCR
Western blotting
Flow cytometry analysis of cell cycle and apoptosis
The genome-wide transcriptiomic analysis
QUANTIFICATION AND STATISTICAL ANALYSIS
Study approval
AUTHOR CONTRIBUTIONS
L.Q. designed and performed most of the experiments except indicated elsewhere, made all figures and wrote the manuscript draft. M.W. performed the statistical analysis of transcriptome data. Y.R. participated in the preparation of gene knockout cell lines. X.R. and S.H. participated in animal experiments. S.W. provided critical suggestion and invaluable materials to improve the work. Y.Z. designed and supervised this study, interpreted all data, generated project resources, and wrote the manuscript. All authors reviewed and commented on the manuscript. Meanwhile, these authors declare no competing financial and other interests.
STAR+METHODS
KEY RESOURCES TABLE
CONTACT FOR REAGENT AND RESOURCE SHARING
Further information and requests for resources and reagents should be directed to and will be fulfilled by the Lead Contact, Yiguo Zhang (yiguozhang{at}cqu.edu.cn)
EXPERIMENTAL MODEL AND SUBJECT DETAILS
Animal care and use
In this study, the relevant animal experiments were indeed conducted according to the valid ethical regulations that have been approved. All mice were maintained under standard animal housing conditions with a 12-h dark cycle and allowed access ad libitum to sterilized water and diet. All relevant studies were carried out on 8-week-old male mice (with the license No. PIL60/13167) in accordance with the United Kingdom Animal (Scientific Procedures) Act (1986) and the guidelines of the Animal Care and Use Committees of Chongqing University and the Third Military Medical University, both of which were subjected to the local ethical review (in China). All relevant experimental protocols were approved by the University Laboratory Animal Welfare and Ethics Committee (with two institutional licenses SCXK-PLA-20120011 and SYXK-PLA-20120031).
Mouse embryonic fibroblasts (MEFs)
The wild-type MEF and MEFNrf1−/−(ΔDBD) cell lines (in which ΔDBD represents deletion of mouse Nrf1 DNA-binding domain (DBD)-adjoining codon sequence) were provided as a gift by Dr. Akira Kobayashi (Doshisha University, Japan). Additional wild-type MEF and MEFNrf2−/−(ΔDBD), and MEFKeap1−/− were from Prof. John D. Hayes (University of Dundee, UK). In fact, it should also be credited to Prof. Masayuki Yamamoto (Tohoku University, Japan) because all relevant mouse lines were originally made in his laboratory.
Human liver cell lines with distinct genotypes
All four cell lines Nrf1α−/−, Nrf1α−/−+siNrf2, Nrf2−/−ΔTA and caNrf2ΔN were created in this study. Their progenitor cells are the human hepatocellular carcinoma (HepG2) and/or another non-cancerous human liver (HL7702) cell lines. The latter two lines HepG2 and HL7702 are wild-type (Nrf1/2+/+, Keap1+/+) cells, because not any mutants in the Nrf1, Nrf2 and Keap1 genes are therein confirmed by sequencing. However, it is important to be noted that Nrf1 and its long TCF11 isoform are co-expressed at a ratio of 1:1 in HL7702 cells. By contrast, significantly decreased expression of Nrf1 is observed in HepG2 cells (Ren et al., 2016), while almost none of its longer TCF11 transcripts were detected. For relevant identification of these cell lines, see Figures 1 and S1.
METHODS DETAILS
Cell culture and transfection
Cells were grown in DMEM supplemented with 5 mM glutamine, 10% (v/v) foetal bovine serum (FBS), 100 units/ml of either of penicillin and streptomycin, in the 37 °C incubator with 5% CO2. The experimental cells were transfected with indicated plasmids alone or in combination for 8 h using Lipofectamine® 3000 Transfection Kit (Invitrogen, USA), and then allowed for recovery from transfection in the fresh medium for 24 h before being subjected to indicated experiments.
Expression constructs and other oligos used for siRNA and miRNA
Expression constructs for human Nrf1, Nrf2, JUN and FOS were made by cloning each of their full-length cDNA sequences into a pcDNA3 vector, respectively. Notably, the other plasmids specifically for the genome-editing of Nrf1 or Nrf2 by Talens or CRISPR/Cas9 were created (in Figure S1) and identified (in Figure 1). Furtherly, we were made four specific luciferase reporters, which were driven by distinct gene promoter regions from the human Nrf1, Nrf2, COX1 and COX2. Different lengths of these gene promoter regions were amplified by PCR from their genomic loci and inserted into the PGL3-basic vector. In addition to these intact reporter genes PNrf1-Luc, PNrf2-Luc, PCOX1-Luc, PCOX2-Luc and miR22-ARE-Luc, all these relevant ARE-specific mutant reporters were engineered. Moreover, double fluorescent reporters (i.e. PTEN-miR22b and COX1-miR22b) were created by cloning the 3’ UTR region sequences of COX1 and PTEN, that were amplified from reverse transcription PCR products and ligated into the psiCHECK2 vector. All primers and other oligos used for siRNAs and Mir-RNAs were synthesized by Sangon Biotech (Shanghai, China). The fidelity of all constructs used in this study was confirmed to be true by sequencing.
Subcutaneous tumor xenografts in nude mice
Mouse xenograft models were made by subcutaneous heterotransplantation of the human hepatoma HepG2 (i.e. Nrf1/2+/+ or each derivate of Nrf1α−/−, Nrf1α−/−+siNrf2, Nrf2−/−ΔTA and caNrf2ΔN cell lines into nude mice, as described (Morton and Houghton, 2007). Experimental human hepatoma cells (1 × 107, allowed for growth in the exponential phase) were suspended in 0.2 ml of serum-free DMEM and were inoculated subcutaneously into the right upper back region of male nude mice (BALB/Cnu/nu, 6 weeks, 18 g, from HFK Bioscience, Beijing) at a single site. The procedure of injection into all mice was completed within 30 min, and the formation of the subcutaneous tumour exnografts was observed. Once the tumor exnografts emerged, their sizes were successively measured once every two days, until the 32nd day when the mice were sacrificed before the transplanted tumors were excised. The sizes of growing tumors were calculated by a standard formula (i.e. V = ab2/2) and then are shown graphically (n = 6 per group). Subsequently, the tumor tissues were also subjected to the histopathological examination by the routine hematoxylin-eosin staining. Notably, all the relevant animal experiments in this study were indeed conducted according to the valid ethical regulations that have been approved.
Histology
Xenograft tumor tissues were immersed in 4% paraformaldehyde for overnight and then transferred to 70% ethanol. Individual tumor tissues were placed in processing cassettes, dehydrated through a serial of alcohol gradient, and embedded in paraffin wax blocks. Before staining, the tissue sections were de-waxed in xylene, rehydrated through decreasing concentrations of ethanol, and washed in PBS. Lastly, they were stained with hematoxylin and eosin (H&E), and visualized by microscopy.
Lipid staining
Experimental cells were seeded in 6-well plates and cultured with 200 µM sodium oleate (Solarbio, Beijing, China) medium. The cells were fixed for 30 min with 4% paraformaldehyde (AR1068, Boster Biological Technology, Wuhan, China) and then stained for 30 min with a solution of 3 g/L oil red O (A600395, Sangon Biotech, Shanghai, China). The stained cells were rinsed 3 times with 60 % of isopropyl alcohol (Kelong, Chengdu, China) before the red lipid droplets were visualized by microscopy.
Cellular ROS staining
Experimental cells were allowed for growth to an appropriate confluence in 6-well plates and then incubated in serum-free medium containing 10 µM of 2’,7’-Dichlorodihydrofluorescein diacetate (DCFH-DA) (S0033, Beyotime, Shanghai, China) at 37°C for 20 min. Thereafter, the cells were washed three times with serum-free medium, before the green fluorescent images were achieved by microscopy.
Luciferase reporter assay
Equal numbers (1.0×105) of experimental cells were seeded into each well of the 12-well plates. After reaching 80% confluence, the cells were transfected with a Lipofectamine 3000 mixture with luciferase plasmids with or without other expression plasmids. In the pGL3 plasmid system, the Renilla-luciferase, which expression by pRL-TK plasmid, as an internal control for transfection efficiency. And in the psi-CHECK2 plasmid system, the Pyralis-luciferase activity is the internal control, while the Renilla-luciferase activity is the experimental test object. The luciferase activity was measured by using the dual-luciferase reporter assay system (E1910, Promega). The resultant data were normalized as a fold change (mean ± S.D) relative to the activity of the control group (at a given value of 1.0). The data presented here represent at least 3 independent experiments undertaken on separate occasions that were each performed in triplicate. Significant differences in the transcriptional activity were subjected to statistical analysis.
Real-time quantitative PCR
Experimental cells were subjected to isolation of total RNAs by using the RNAsimple Kit (Tiangen Biotech CO., Beijing). Subsequently, 500 ng of total RNAs were added in a reverse-transcriptase reaction to generate the first strand of cDNA (with Revert Aid First Strand Synthesis Kit from Thermo). The synthesized cDNA was served as the template for qPCR, in the GoTaq® qPCR Master Mix (from Promega), before being deactivated at 95°C for 10 min, and amplified by 40 reaction cycles of the annealing at 95°C for 15 s and then extending at 60°C for 30 s. The final melting curve was validated to examine the amplification quality, whereas the mRNA expression level of β-actin served as an optimal internal standard control.
Western blotting
Experimental cells were harvested in a lysis buffer (0.5% SDS, 0.04 mol/L DTT, pH 7.5), which was supplemented with the protease inhibitor cOmplete Tablets EASYpack or phosphatase inhibitor PhosSTOP EASYpack (either 1 tablet per 10 mL, Roche, Germany). The lysates were denatured immediately at 100°C for 10 min, sonicated sufficiently, and diluted in 3× loading buffer (187.5 mmol/L Tris-HCl, pH 6.8, 6% SDS, 30% Glycerol, 150 mmol/L DTT, 0.3% Bromphenol Blue) at 100°C for 5 min. Subsequently, equal amounts of protein extracts were subjected to separation of proteins by SDS-PAGE containing 4-15% polyacrylamide, and then visualization by Western blotting with distinct antibodies as indicated. On some occasions, the blotted membranes were stripped for 30 min and then re-probed with additional primary antibodies. β-actin served as an internal control to verify equal loading of proteins in each of electrophoretic wells.
Flow cytometry analysis of cell cycle and apoptosis
Experimental cells (5 × 105) were allowed for growth in 60-mm cell culture plate for 48 h and synchronization by 12-h starvation in a serum-free medium, before being treated with 10 μmol/L BrdU for 12 h. The cells were fixed for 15 min with 100 μl of BD Cytofix/Cytoperm buffer (containing a mixture of the fixative paraformaldehyde and the detergent saponin) at room temperature and permeabilized for 10 min with 100 μl of BD Cytoperm permeabilization buffer plus (containing fetal bovine serum as a staining enhancer) on ice. Thereafter, the cells were re-fixed and treated with 100 μl of DNase (at a dose of 300 μg/ml in PBS) for 1 h at 37 °C, in order to expose the incorporated BrdU, followed by staining with FITC conjugated anti-BrdU antibody for 60 min at room temperature. Subsequently, the cells were suspended in 20 μl of 7-amino-actinomycin D solution 20 min for the DNA staining and re-suspended in 0.5 ml of a staining buffer (i.e. 1 × DPBS containing 0.09% sodium azide and 3% heat-inactivated FBS), prior to the cell cycle analysis by flow cytometry. Furthermore, additional fractions of cells (5 × 105) were allowed for 48 h growth in 60-mm cell culture plate before being used for apoptosis analysis. The cells were pelleted by centrifuging at 1000 × g for 5 min and washed by PBS for three times, before being incubated for 15 min with 5 μl of Annexin V-FITC and 10 μl of propidium iodide (PI) in 195 μl of the binding buffer, prior to flow cytometry analysis of cell apoptosis. The results being analyzed by the FlowJo 7.6.1 software.
The genome-wide transcriptomic analysis
Total RNAs were subjected to the sequencing by the Beijing Genomics Institute (BGI, www.genomics.org.cn) on the platform of BGISEQ-500 (contract No. is F17FTSCCWLJ1161). After removing the ‘dirty’ raw reads with data filtering, the clean reads were generated and mapped to the reference by using both HISAT (Kim et al., 2015) and Bowtie2 (Langmead et al., 2009) tools. Of note, gene expression levels were calculated by using the FPKM (Fragments Per Kilobase of exon model per Million mapped fragments) method with RSEM (Li and Dewey, 2011). Then, differentially expressed genes (DEGs) were identified with the criteria Fold-change ≥2 and diverge probability ≥0.8 by using the NOISeq (Tarazona et al., 2011). For the functional annotation, all DEGs were mapped to gene ontology (GO) terms in the database (http://www.geneontology.org/) and the pathway enrichment analysis of DEGs was performed by using KEGG (Kanehisa et al., 2008).
QUANTIFICATION AND STATISTICAL ANALYSIS
Significant differences were statistically determined using the Student’s t-test and Multiple Analysis of Variations (MANOVA). The data are here shown as a fold change (mean ± S.D.), each of which represents at least 3 independent experiments that were each performed in triplicate.
Study approval
All experimental procedures were approved by the Animal Care and Use Committees of Chongqing University and the Third Military Medical University, both of which were subjected to the local ethical review (in China). Randomly assigned nude mice were injected subcutaneously with distinct cell lines as experimented.
ACKNOWLEDGMENTS
We are grateful to Dr. Akira Kobayashi (at Doshisha University, Japan) for providing both Nrf1−/−(ΔDBD) and Nrf1+/+ MEF lines as a gift. The work was supported by the National Natural Science Foundation of China (81872336, 91129703, 91429305, and 31270879) awarded to Prof. Yiguo Zhang (University of Chongqing, China), and also funded in part by Chongqing University postgraduates′ innovation project (No. CYB15024) funded to Mr. Lu Qiu.