| Literature DB >> 32375051 |
Enrique M Toledo1, Shanzheng Yang1, Daniel Gyllborg1, Kim E van Wijk1, Indranil Sinha2, Manuel Varas-Godoy1, Christopher L Grigsby3, Peter Lönnerberg1, Saiful Islam1, Knut R Steffensen4, Sten Linnarsson1, Ernest Arenas5.
Abstract
Liver X receptors (LXRs) and their ligands are potent regulators of midbrain dopaminergic (mDA) neurogenesis and differentiation. However, the molecular mechanisms by which LXRs control these functions remain to be elucidated. Here, we perform a combined transcriptome and chromatin immunoprecipitation sequencing (ChIP-seq) analysis of midbrain cells after LXR activation, followed by bioinformatic analysis to elucidate the transcriptional networks controlling mDA neurogenesis. Our results identify the basic helix-loop-helix transcription factor sterol regulatory element binding protein 1 (SREBP1) as part of a cluster of proneural transcription factors in radial glia and as a regulator of transcription factors controlling mDA neurogenesis, such as Foxa2. Moreover, loss- and gain-of-function experiments in vitro and in vivo demonstrate that Srebf1 is both required and sufficient for mDA neurogenesis. Our data, thus, identify Srebf1 as a central player in mDA neurogenesis.Entities:
Keywords: FOXA2; LXR; Parkinson disease; bHLH; chromatin immunoprecipitation; development; nuclear receptor; oxysterol; radial glia; single-cell RNA sequencing; transcriptional network
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Year: 2020 PMID: 32375051 DOI: 10.1016/j.celrep.2020.107601
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423