Histone chaperone Asf1 is required for histone H3 lysine 56 acetylation, a modification associated with S phase in mitosis and meiosis

被引:211
作者
Recht, J
Tsubota, T
Tansy, JC
Diaz, RL
Berger, JM
Zhang, X
Garcia, BA
Shabanowitzn, J
Burlingame, AL
Hunt, DF
Kaufman, PD
Allis, CD
机构
[1] Rockefeller Univ, Lab Chromatin Biol, New York, NY 10021 USA
[2] Univ Massachusetts, Sch Med, Program Gene Funct & Express, Worcester, MA 01601 USA
[3] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[4] Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Mass Spectrometry Facil, San Francisco, CA 94143 USA
[6] Univ Virginia, Dept Chem, Charlottesville, VA 22901 USA
关键词
chromatin assembly; H3K56ac; DNA damage;
D O I
10.1073/pnas.0601676103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Histone acetylation affects many nuclear processes including transcription, chromatin assembly, and DNA damage repair. Acetylation of histone H3 lysine 56 (H3 K56ac) in budding yeast occurs during mitotic S phase and persists during DNA damage repair. Here, we show that H3 K56ac is also present during premeiotic S phase and is conserved in fission yeast. Furthermore, the H3 K56ac modification is not observed in the absence of the histone chaperone Asf1. asf1 Delta and H3 K56R mutants exhibit similar sensitivity to DNA damaging agents. Mutational analysis of Asf1 demonstrates that DNA damage sensitivity correlates with (i) decreased levels of H3 K56ac and (ii) a region implicated in histone binding. In contrast, multiple asf1 mutants that are resistant to DNA damage display WT levels of K56ac. These data suggest that maintenance of H3 K56 acetylation is a primary contribution of Asf1 to genome stability in yeast.
引用
收藏
页码:6988 / 6993
页数:6
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