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Distinct Requirements of CHD4 during B Cell Development and Antibody Response

Authors :
Wei-Feng Yen
Rahul Sharma
Montserrat Cols
Colleen M. Lau
Ashutosh Chaudhry
Priyanka Chowdhury
William T. Yewdell
Bharat Vaidyanathan
Amy Sun
Maryaline Coffre
Joseph N. Pucella
Chun-Chin Chen
Maria Jasin
Joseph C. Sun
Alexander Y. Rudensky
Sergei B. Koralov
Jayanta Chaudhuri
Source :
Cell Reports, Vol 27, Iss 5, Pp 1472-1486.e5 (2019)
Publication Year :
2019
Publisher :
Elsevier, 2019.

Abstract

Summary: The immunoglobulin heavy chain (Igh) locus features a dynamic chromatin landscape to promote class switch recombination (CSR), yet the mechanisms that regulate this landscape remain poorly understood. CHD4, a component of the chromatin remodeling NuRD complex, directly binds H3K9me3, an epigenetic mark present at the Igh locus during CSR. We find that CHD4 is essential for early B cell development but is dispensable for the homeostatic maintenance of mature, naive B cells. However, loss of CHD4 in mature B cells impairs CSR because of suboptimal targeting of AID to the Igh locus. Additionally, we find that CHD4 represses p53 expression to promote B cell proliferation. This work reveals distinct roles for CHD4 in B cell development and CSR and links the H3K9me3 epigenetic mark with AID recruitment to the Igh locus. : Yen et al. demonstrate that CHD4, a component of the NuRD remodeling complex, is essential for early B cell development, represses p53 expression in mature B cells, and influences the recruitment of AID to DNA during class switch recombination. Keywords: class switch recombination, NuRD complex, germinal centers, CHD4, chromatin remodeling, H3K9me3, p53, AID

Subjects

Subjects :
Biology (General)
QH301-705.5

Details

Language :
English
ISSN :
22111247
Volume :
27
Issue :
5
Database :
Directory of Open Access Journals
Journal :
Cell Reports
Publication Type :
Academic Journal
Accession number :
edsdoj.2f3bea71bc4f469ef90f6397a16508
Document Type :
article
Full Text :
https://doi.org/10.1016/j.celrep.2019.04.011