A brain-specific <i>pgc1</i>α fusion transcript affects gene expression and behavioural outcomes in mice
Oswaldo A. Lozoya, Fu‐Hua Xu, Dagoberto Grenet, Tianyuan Wang, Korey D. Stevanovic, Jesse D. Cushman, Thomas Hagler, Artiom Gruzdev, Patricia Jensen, Bairon Hernández, Gonzalo Riadi, Sheryl S. Moy, Janine H. Santos, Richard P. Woychik
Abstract
PGC1α is a transcriptional coactivator in peripheral tissues, but its function in the brain remains poorly understood. Various brain-specific Pgc1 α isoforms have been reported in mice and humans, including two fusion transcripts (FTs) with non-coding repetitive sequences, but their function is unknown. The FTs initiate at a simple sequence repeat locus ∼570 Kb upstream from the reference promoter; one also includes a portion of a short interspersed nuclear element (SINE). Using publicly available genomics data, here we show that the SINE FT is the predominant form of Pgc1 α in neurons. Furthermore, mutation of the SINE in mice leads to altered behavioural phenotypes and significant up-regulation of genes in the female, but not male, cerebellum. Surprisingly, these genes are largely involved in neurotransmission, having poor association with the classical mitochondrial or antioxidant programs. These data expand our knowledge on the role of Pgc1 α in neuronal physiology and suggest that different isoforms may have distinct functions. They also highlight the need for further studies before modulating levels of Pgc1 α in the brain for therapeutic purposes.