Cell Reports (Apr 2019)

Distinct Requirements of CHD4 during B Cell Development and Antibody Response

  • 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

Journal volume & issue
Vol. 27, no. 5
pp. 1472 – 1486.e5

Abstract

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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