Antibody Class Switching Mediated by Yeast Endonuclease-Generated DNA Breaks

Author:

Zarrin Ali A.12,Del Vecchio Catherine12,Tseng Eva12,Gleason Megan12,Zarin Payam12,Tian Ming12,Alt Frederick W.12

Affiliation:

1. Howard Hughes Medical Institute, Children's Hospital, CBR Institute for Biomedical Research, and Department of Genetics, Harvard University Medical School, Boston, MA 02115, USA.

2. Department of Molecular Genetics and Microbiology, University of Texas at Austin, Austin, TX 78712, USA.

Abstract

Antibody class switching in activated B cells uses class switch recombination (CSR), which joins activation-induced cytidine deaminase (AID)–dependent double-strand breaks (DSBs) within two large immunoglobulin heavy chain (IgH) locus switch (S) regions that lie up to 200 kilobases apart. To test postulated roles of S regions and AID in CSR, we generated mutant B cells in which donor Sμ and accepter Sγ1 regions were replaced with yeast I-SceI endonuclease sites. We found that site-specific I-SceI DSBs mediate recombinational IgH locus class switching from IgM to IgG 1 without S regions or AID. We propose that CSR evolved to exploit a general DNA repair process that promotes joining of widely separated DSBs within a chromosome.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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