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Histone chaperone Spt6 is required for class switch recombination but not somatic hypermutation.


ABSTRACT: Activation-induced cytidine deaminase (AID) is shown to be essential and sufficient to induce two genetic alterations in the Ig loci: class switch recombination (CSR) and somatic hypermutation (SHM). However, it is still unknown how a single-molecule AID differentially regulates CSR and SHM. Here we identified Spt6 as an AID-interacting protein by yeast two-hybrid screening and immunoprecipitation followed by mass spectrometry. Knockdown of Spt6 resulted in severe reduction of CSR in both the endogenous Ig locus in B cells and an artificial substrate in fibroblast cells. Conversely, knockdown of Spt6 did not reduce but slightly enhanced SHM in an artificial substrate in B cells, indicating that Spt6 is required for AID to induce CSR but not SHM. These results suggest that Spt6 is involved in differential regulation of CSR and SHM by AID.

SUBMITTER: Okazaki IM 

PROVIDER: S-EPMC3093487 | biostudies-literature | 2011 May

REPOSITORIES: biostudies-literature

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Histone chaperone Spt6 is required for class switch recombination but not somatic hypermutation.

Okazaki Il-mi IM   Okawa Katsuya K   Kobayashi Maki M   Yoshikawa Kiyotsugu K   Kawamoto Shimpei S   Nagaoka Hitoshi H   Shinkura Reiko R   Kitawaki Yoko Y   Taniguchi Hisaaki H   Natsume Tohru T   Iemura Shun-Ichiro S   Honjo Tasuku T  

Proceedings of the National Academy of Sciences of the United States of America 20110425 19


Activation-induced cytidine deaminase (AID) is shown to be essential and sufficient to induce two genetic alterations in the Ig loci: class switch recombination (CSR) and somatic hypermutation (SHM). However, it is still unknown how a single-molecule AID differentially regulates CSR and SHM. Here we identified Spt6 as an AID-interacting protein by yeast two-hybrid screening and immunoprecipitation followed by mass spectrometry. Knockdown of Spt6 resulted in severe reduction of CSR in both the en  ...[more]

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