Abstract
Antisense transcription is widespread in genomes. Despite large differences in gene size and architecture, we find that yeast and human genes share a unique, antisense transcription-associated chromatin signature. We asked whether this signature is related to a biological function for antisense transcription. Using quantitative RNA-FISH, we observed changes in sense transcript distributions in nuclei and cytoplasm as antisense transcript levels were altered. To determine the mechanistic differences underlying these distributions, we developed a mathematical framework describing transcription from initiation to transcript degradation. At GAL1, high levels of antisense transcription alters sense transcription dynamics, reducing rates of transcript production and processing, while increasing transcript stability, which is also a genome-wide association. Establishing the antisense transcription-associated chromatin signature through disruption of the Set3C histone deacetylase activity is sufficient to similarly change these rates even in the absence of antisense transcription. Thus, antisense transcription alters sense transcription dynamics in a chromatin-dependent manner.
In this work, Brown et al. provide a mechanistic understanding of the effect of antisense transcription on the production and fate of sense transcripts. Antisense transcription buffers genes against the action of the Set3 lysine deacetylase, thus altering rates of transcript production, processing and stability.
Conserved antisense transcription-dependent chromatin architecture near promoters
Antisense transcription alters sense transcription dynamics and transcript stability
Antisense transcription functions in a chromatin-dependent manner
Increased acetylation by set3Δ mimics high antisense transcriptional dynamics