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NME proteins regulate class switch recombination.
Zheng, Simin; Kusnadi, Anthony; Choi, Jee Eun; Vuong, Bao Q; Rhodes, Daniela; Chaudhuri, Jayanta.
Afiliação
  • Zheng S; Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Kusnadi A; Immunology and Microbial Pathogenesis Program, Weill Cornell Graduate School of Medical Sciences, New York, NY, USA.
  • Choi JE; NTU Institute of Structural Biology, Nanyang Technological University, Singapore, Singapore.
  • Vuong BQ; Immunology and Microbial Pathogenesis Program, Weill Cornell Graduate School of Medical Sciences, New York, NY, USA.
  • Rhodes D; Arthritis and Tissue Degeneration Program and Genomics Center, Hospital for Special Surgery, New York, NY, USA.
  • Chaudhuri J; Department of Biology, City College of New York, NY, USA.
FEBS Lett ; 593(1): 80-87, 2019 01.
Article em En | MEDLINE | ID: mdl-30411342
ABSTRACT
Class switch recombination (CSR) in B cells involves deletion-recombination at switch (S) region DNA and is important for the diversification of antibody isotypes during an immune response. Here, we identify two NME [NM23/NDPK (nucleoside diphosphate kinase)] isoforms, NME1 and NME2, as novel players in this process. Knockdown of NME2 leads to decreased CSR, while knockdown of the highly homologous NME1 results in increased CSR. Interestingly, these NME proteins also display differential occupancy at S regions during CSR despite their homology; NME1 binds to S regions prior to stimulation, while NME2 binds to S regions only after stimulation. To the best of our knowledge, this represents the first report of a role for these proteins in the regulation of CSR.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfócitos B / Cadeias Pesadas de Imunoglobulinas / Nucleosídeo NM23 Difosfato Quinases Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: FEBS Lett Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfócitos B / Cadeias Pesadas de Imunoglobulinas / Nucleosídeo NM23 Difosfato Quinases Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: FEBS Lett Ano de publicação: 2019 Tipo de documento: Article