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
Affiliations
Wei-Feng Yen
Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA; Biochemistry, Cellular and Molecular Biology Program, Weill Graduate School of Medical Sciences, New York, NY, USA
Rahul Sharma
Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA
Montserrat Cols
Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA
Colleen M. Lau
Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA
Ashutosh Chaudhry
Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA
Priyanka Chowdhury
Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA; Immunology and Microbial Pathogenesis Program, Weill Cornell Graduate School of Medical Sciences, New York, NY, USA
William T. Yewdell
Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA
Bharat Vaidyanathan
Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA; Immunology and Microbial Pathogenesis Program, Weill Cornell Graduate School of Medical Sciences, New York, NY, USA
Amy Sun
Department of Pathology, New York University School of Medicine, New York, NY, USA
Maryaline Coffre
Department of Pathology, New York University School of Medicine, New York, NY, USA
Joseph N. Pucella
Gerstner Sloan Kettering Graduate School of Biomedical Sciences, New York, NY, USA
Chun-Chin Chen
Biochemistry, Cellular and Molecular Biology Program, Weill Graduate School of Medical Sciences, New York, NY, USA; Developmental Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA
Maria Jasin
Biochemistry, Cellular and Molecular Biology Program, Weill Graduate School of Medical Sciences, New York, NY, USA; Gerstner Sloan Kettering Graduate School of Biomedical Sciences, New York, NY, USA; Developmental Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA
Joseph C. Sun
Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA; Immunology and Microbial Pathogenesis Program, Weill Cornell Graduate School of Medical Sciences, New York, NY, USA; Gerstner Sloan Kettering Graduate School of Biomedical Sciences, New York, NY, USA
Alexander Y. Rudensky
Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA; Immunology and Microbial Pathogenesis Program, Weill Cornell Graduate School of Medical Sciences, New York, NY, USA; Gerstner Sloan Kettering Graduate School of Biomedical Sciences, New York, NY, USA; Howard Hughes Medical Institute, Memorial Sloan Kettering Cancer Center, New York, NY, USA
Sergei B. Koralov
Department of Pathology, New York University School of Medicine, New York, NY, USA
Jayanta Chaudhuri
Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA; Immunology and Microbial Pathogenesis Program, Weill Cornell Graduate School of Medical Sciences, New York, NY, USA; Gerstner Sloan Kettering Graduate School of Biomedical Sciences, New York, NY, USA; Corresponding author
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