Distinct Requirements of CHD4 during B Cell Development and Antibody Response. Academic Article uri icon

Overview

abstract

  • 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.

publication date

  • April 30, 2019

Research

keywords

  • B-Lymphocytes
  • Cell Proliferation
  • DNA Helicases
  • Immunoglobulin Class Switching

Identity

PubMed Central ID

  • PMC6527137

Scopus Document Identifier

  • 85064604484

Digital Object Identifier (DOI)

  • 10.1016/j.celrep.2019.04.011

PubMed ID

  • 31042474

Additional Document Info

volume

  • 27

issue

  • 5