Chd5 Regulates the Transcription Factor Six3 to Promote Neuronal Differentiation

Author:

Shrestha Padmina12ORCID,Jaganathan Anbalagan1,Huilgol Dhananjay13,Ballon Carlos1,Hwangbo Yon1,Mills Alea A1ORCID

Affiliation:

1. Cold Spring Harbor Laboratory , Cold Spring Harbor, NY , USA

2. Department of Molecular and Cell Biology, Stony Brook University , Stony Brook, NY , USA

3. Department of Neurobiology, Duke University Medical Center , Durham, NC , USA

Abstract

Abstract Chromodomain helicase DNA-binding protein 5 (Chd5) is an ATP-dependent chromatin remodeler that promotes neuronal differentiation. However, the mechanism behind the action of Chd5 during neurogenesis is not clearly understood. Here we use transcriptional profiling of cells obtained from Chd5 deficient mice at early and late stages of neuronal differentiation to show that Chd5 regulates neurogenesis by directing stepwise transcriptional changes. During early stages of neurogenesis, Chd5 promotes expression of the proneural transcription factor Six3 to repress Wnt5a, a non-canonical Wnt ligand essential for the maturation of neurons. This previously unappreciated ability of Chd5 to transcriptionally repress neuronal maturation factors is critical for both lineage specification and maturation. Thus, Chd5 facilitates early transcriptional changes in neural stem cells, thereby initiating transcriptional programs essential for neuronal fate specification.

Funder

Cold Spring Harbor Laboratory

National Cancer Institute

National Institutes of Health

Office of the Director

Human Frontier Science Program

NARSAD

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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