Diverse Roles for Histone H2A Modifications in DNA Damage Response Pathways in Yeast
Author(s) -
John Moore,
Oya Yazgan,
Yeganeh Ataian,
Jocelyn E. Krebs
Publication year - 2006
Publication title -
genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.792
H-Index - 246
eISSN - 1943-2631
pISSN - 0016-6731
DOI - 10.1534/genetics.106.063792
Subject(s) - dna repair , dna damage , biology , homologous recombination , chromatin , histone , histone h2a , genetics , ku80 , dna repair protein xrcc4 , nucleotide excision repair , dna , dna damage repair , dna mismatch repair , homology directed repair , microbiology and biotechnology , non homologous end joining , computational biology , gene , dna binding protein , transcription factor
There are many types of DNA damage that are repaired by a multiplicity of different repair pathways. All damage and repair occur in the context of chromatin, and histone modifications are involved in many repair processes. We have analyzed the roles of H2A and its modifications in repair by mutagenizing modifiable residues in the N- and C-terminal tails of yeast H2A and by testing strains containing these mutations in multiple DNA repair assays. We show that residues in both tails are important for homologous recombination and nonhomologous end-joining pathways of double-strand break repair, as well as for survival of UV irradiation and oxidative damage. We show that H2A serine 122 is important for repair and/or survival in each of these assays. We also observe a complex pattern of H2A phosphorylation at residues S122, T126, and S129 in response to different damage conditions. We find that overlapping but nonidentical groups of H2A residues in both tails are involved in different pathways of repair. These data suggest the presence of a set of H2A "damage codes" in which distinct patterns of modifications on both tails of H2A may be used to identify specific types of damage or to promote specific repair pathways.
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