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

Jingsong Yuan, Rachel Adamski, Junjie Chen

Research output: Contribution to journalReview articlepeer-review

239 Scopus citations

Abstract

Phosphorylation of histone variant H2AX at serine 139, named γH2AX, has been widely used as a sensitive marker for DNA double-strand breaks (DSBs). γH2AX 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.

Original languageEnglish (US)
Pages (from-to)3717-3724
Number of pages8
JournalFEBS Letters
Volume584
Issue number17
DOIs
StatePublished - Sep 2010

Keywords

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

ASJC Scopus subject areas

  • Biophysics
  • Structural Biology
  • Biochemistry
  • Molecular Biology
  • Genetics
  • Cell Biology

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