Abstract: Neurodegenerative diseases that affect the motor neurons, including amyotrophic lateral sclerosis (ALS), have little treatment options and are generally rapidly fatal (1, 2). We harnessed the power of unbiased, whole transcriptome differential gene expression analysis, utilizing primary patient cells and tissues to discover genes whose expression defines ALS using published data (3, 4). We found significant differential expression of BIK, encoding BCL2-interacting killer, in the induced pluripotent stem cell (iPSC)-derived motor neurons of patients with ALS. BIK was also differentially expressed in iPSC-derived motor neurons in a separate microarray dataset (4). BIK transcript was present at significantly higher levels in ALS patient motor neurons as compared to control motor neurons. These analyses will begin to define the transcriptional landscape of ALS.

Journal Link: 10.31219/osf.io/qfmd4 Journal Link: Publisher Website Journal Link: Google Scholar