4.5 Review

Focus on histone variant H2AX: To be or not to be

期刊

FEBS LETTERS
卷 584, 期 17, 页码 3717-3724

出版社

WILEY
DOI: 10.1016/j.febslet.2010.05.021

关键词

H2AX; MRE11/RAD50/NBS1; DNA damage; DNA repair; Non-homologous end-joining; Homologous recombination

资金

  1. National Institutes of Health [CA089239, CA092312, CA100109]
  2. Department of Defense [W81XWH-05-1-0470]
  3. M.D. Anderson Cancer Center [CA016672]

向作者/读者索取更多资源

Phosphorylation of histone variant H2AX at serine 139, named gamma H2AX, has been widely used as a sensitive marker for DNA double-strand breaks (DSBs). gamma H2AX is required for the accumulation of many DNA damage response (DDR) proteins at DSBs. Thus it is believed to be the principal signaling protein involved in DDR and to play an important role in DNA repair. However, only mild defects in DNA damage signaling and DNA repair were observed in H2AX-deficient cells and animals. Such findings prompted us and others to explore H2AX-independent mechanisms in DNA damage response. Here, we will review recent advances in our understanding of H2AX-dependent and independent DNA damage signaling and repair pathways in mammalian cells. (C) 2010 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据