LINE-1 retrotransposon activation intrinsic to interneuron development
Gabriela Oana BodeaiD, Juan Manuel BottoiD, Maria E. FerreiroiD, Francisco Jose Sanchez-LuqueiD, Jose de los Rios Barreda, Jay RasmusseniD, Muhammed A. Rahman, Laura R. FenloniD, Natasha JansziD, Carolina GubertiD, Patricia GerdesiD, Liviu‐Gabriel BodeaiD, Prabha AjjikuttiraiD, Darwin J. Da Costa GuevaraiD, Linda Cumner, Charles C. BelliD, Peter KozuliniD, Victor BilloniD, Santiago Morell, Marie-Jeanne H.C. Kempen, Chloe J. LoveiD, Karabi SahaiD, Lucy M. PalmeriD, Adam D. EwingiD, Dhanisha J. JhaveriiD, , Geoffrey J. FaulkneriD
Abstract
Retrotransposons are a reservoir of cis-regulatory innovation1-3. Developmental programs that activate these elements could, in principle, manifest in lineage-specific retrotransposition. Somatic LINE-1 (L1) retrotransposon insertions have been detected in human and non-human primate neurons4-7. It is however unknown whether L1 is mobile in only some neuronal lineages, or therein regulates neurodevelopmental genes. Here, we report programmed L1 activation by SOX6, a transcription factor critical for parvalbumin (PV) interneuron development8-10. PV+ neurons permit L1 mobilization in vitro and in vivo, harbor unmethylated L1 promoters, and express full-length L1 mRNAs and proteins. Via nanopore long-read sequencing, we identify unmethylated L1 promoters proximal to PV+ neuron genes. One such L1, which promotes transcription of a novel CAPS2 gene isoform, significantly enhances neuron morphological complexity when phenotyped in vitro. These data highlight the contribution made by L1 cis-regulatory elements to PV+ neuron development and transcriptome diversity, uncovered due to L1 mobility in this milieu.
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