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.
Original language | English |
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Article number | 107601 |
Journal | Cell Reports |
Volume | 31 |
Issue number | 5 |
DOIs | |
Publication status | Published - 05 May 2020 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2020 The Author(s)
Keywords
- bHLH
- chromatin immunoprecipitation
- development
- FOXA2
- LXR
- nuclear receptor
- oxysterol
- Parkinson disease
- radial glia
- single-cell RNA sequencing
- transcriptional network
ASJC Scopus subject areas
- General Biochemistry,Genetics and Molecular Biology