TY - JOUR T1 - Gene Expression Signatures of Sporadic ALS Motor Neuron Populations JF - bioRxiv DO - 10.1101/038448 SP - 038448 AU - Ranjan Batra AU - Kasey Hutt AU - Anthony Vu AU - Stuart J. Rabin AU - Michael W. Baughn AU - Ryan T. Libby AU - Shawn Hoon AU - John Ravits AU - Gene W. Yeo Y1 - 2016/01/01 UR - http://biorxiv.org/content/early/2016/02/03/038448.abstract N2 - Background Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease primarily affecting motor neurons (MNs) to cause progressive paralysis. Ninety percent of cases are sporadic (sALS) and ten percent are familial (fALS). The molecular mechanisms underlying neurodegeneration remain elusive and there is a lack of promising biomarkers that define ALS phenotypes and progression. To date, most expression studies have focused on either complex whole tissues that contain cells other than MNs or induced pluripotent derived MNs (iMNs). Furthermore, as human tissue samples have high variability, estimation of differential gene-expression is not a trivial task.Results Here, we report a battery of orthogonal computational analyses to discover geneexpression defects in laser capture microdissected and enriched MN RNA pools from sALS patient spinal cords in regions destined for but not yet advanced in neurodegenerative stage. We used total RNA-sequencing (RNA-seq), applied multiple percentile rank (MPR) analysis to analyze MN-specific gene-expression signatures, and used high-throughput qPCR to validate RNA-seq results. Furthermore, we used a systems-level approach that identified molecular networks perturbed in sALS MNs. Weighted gene co-expression correlation network (WGCNA) analysis revealed defects in neurotransmitter biosynthesis and RNA-processing pathways while gene-gene interaction analysis showed abnormalities in networks that pertained to cell-adhesion, immune response and wound healing.Conclusions We discover gene-expression signatures that distinguish sALS from control MNs and our findings illuminate possible mechanisms of cellular toxicity. Our systematic and comprehensive analysis serves as a framework to reveal expression signatures and disrupted pathways that will be useful for future mechanistic studies and biomarker based therapeutic research. ER -