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ATM stabilizes DNA double-strand-break complexes during V(D)J recombination

Author

Listed:
  • Andrea L. Bredemeyer

    (Washington University School of Medicine)

  • Girdhar G. Sharma

    (Washington University School of Medicine)

  • Ching-Yu Huang

    (Washington University School of Medicine)

  • Beth A. Helmink

    (Washington University School of Medicine)

  • Laura M. Walker

    (Washington University School of Medicine)

  • Katrina C. Khor

    (Washington University School of Medicine)

  • Beth Nuskey

    (University of Pennsylvania School of Medicine)

  • Kathleen E. Sullivan

    (University of Pennsylvania School of Medicine)

  • Tej K. Pandita

    (Washington University School of Medicine)

  • Craig H. Bassing

    (University of Pennsylvania School of Medicine
    Abramson Family Cancer Research Institute)

  • Barry P. Sleckman

    (Washington University School of Medicine)

Abstract

Examination of the role of the ATM protein in oncogenic chromosomal translocations in the disease ataxia telangiectasia finds that ATM is involved directly in stabilizing a complex that occurs when DNA double-strand breaks are made in lymphocyte antigen receptor loci. When the complex is not stabilized, the DNA ends are able to undergo aberrant reactions that can lead to translocations.

Suggested Citation

  • Andrea L. Bredemeyer & Girdhar G. Sharma & Ching-Yu Huang & Beth A. Helmink & Laura M. Walker & Katrina C. Khor & Beth Nuskey & Kathleen E. Sullivan & Tej K. Pandita & Craig H. Bassing & Barry P. Slec, 2006. "ATM stabilizes DNA double-strand-break complexes during V(D)J recombination," Nature, Nature, vol. 442(7101), pages 466-470, July.
  • Handle: RePEc:nat:nature:v:442:y:2006:i:7101:d:10.1038_nature04866
    DOI: 10.1038/nature04866
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    Cited by:

    1. Khalid H. Bhat & Saurabh Priyadarshi & Sarah Naiyer & Xinyan Qu & Hammad Farooq & Eden Kleiman & Jeffery Xu & Xue Lei & Jose F. Cantillo & Robert Wuerffel & Nicole Baumgarth & Jie Liang & Ann J. Feene, 2023. "An Igh distal enhancer modulates antigen receptor diversity by determining locus conformation," Nature Communications, Nature, vol. 14(1), pages 1-18, December.
    2. Estelle Vincendeau & Wenming Wei & Xuefei Zhang & Cyril Planchais & Wei Yu & Hélène Lenden-Hasse & Thomas Cokelaer & Juliana Pipoli da Fonseca & Hugo Mouquet & David J. Adams & Frederick W. Alt & Step, 2022. "SHLD1 is dispensable for 53BP1-dependent V(D)J recombination but critical for productive class switch recombination," Nature Communications, Nature, vol. 13(1), pages 1-16, December.

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