Acetylated lysine 56 on histone H3 drives chromatin assembly after repair and signals for the completion of repair

被引:330
作者
Chen, Chin-Chuan [1 ]
Carson, Joshua J. [1 ]
Feser, Jason [1 ]
Tamburini, Beth [1 ]
Zabaronick, Susan [1 ]
Linger, Jeffrey [1 ]
Tyler, Jessica K. [1 ]
机构
[1] Univ Colorado, Sch Med, Dept Biochem & Mol Genet, Aurora, CO 80045 USA
关键词
D O I
10.1016/j.cell.2008.06.035
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DNA damage causes checkpoint activation leading to cell cycle arrest and repair, during which the chromatin structure is disrupted. The mechanisms whereby chromatin structure and cell cycle progression are restored after DNA repair are largely unknown. We show that chromatin reassembly following double- strand break (DSB) repair requires the histone chaperone Asf1 and that absence of Asf1 causes cell death, as cells are unable to recover from the DNA damage checkpoint. We find that Asf1 contributes toward chromatin assembly after DSB repair by promoting acetylation of free histone H3 on lysine 56 (K56) via the histone acetyl transferase Rtt109. Mimicking acetylation of K56 bypasses the requirement for Asf1 for chromatin reassembly and checkpoint recovery, whereas mutations that prevent K56 acetylation block chromatin reassembly after repair. These results indicate that restoration of the chromatin following DSB repair is driven by acetylated H3 K56 and that this is a signal for the completion of repair.
引用
收藏
页码:231 / 243
页数:13
相关论文
共 58 条
[1]   The histone chaperone anti-silencing function 1 stimulates the acetylation of newly synthesized histone H3 in S-phase [J].
Adkins, Melissa W. ;
Carson, Joshua J. ;
English, Christine M. ;
Ramey, Christopher J. ;
Tyler, Jessica K. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (02) :1334-1340
[2]   Chromatin disassembly mediated by the histone chaperone Asf1 is essential for transcriptional activation of the yeast PH05 and PH08 genes [J].
Adkins, MW ;
Howar, SR ;
Tyler, JK .
MOLECULAR CELL, 2004, 14 (05) :657-666
[3]   Genome instability:: a mechanistic view of its causes and consequences [J].
Aguilera, Andres ;
Gomez-Gonzalez, Belen .
NATURE REVIEWS GENETICS, 2008, 9 (03) :204-217
[4]   Histone modifications in response to DNA damage [J].
Altaf, Mohammed ;
Saksouk, Nehme ;
Cote, Jacques .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2007, 618 (1-2) :81-90
[5]   DNA damage activates ATM through intermolecular autophosphorylation and dimer dissociation [J].
Bakkenist, CJ ;
Kastan, MB .
NATURE, 2003, 421 (6922) :499-506
[6]   DNA damage checkpoints: from initiation to recovery or adaptation [J].
Bartek, Jiri ;
Lukas, Jiri .
CURRENT OPINION IN CELL BIOLOGY, 2007, 19 (02) :238-245
[7]   The sirtuins Hst3 and Hst4p preserve genome integrity by controlling histone H3 lysine 56 deacetylation [J].
Celic, Ivana ;
Masumoto, Hiroshi ;
Griffith, Wendell P. ;
Meluh, Pamela ;
Cotter, Robert J. ;
Boeke, Jef D. ;
Verreault, Alain .
CURRENT BIOLOGY, 2006, 16 (13) :1280-1289
[8]   A role for Saccharomyces cerevisiae histone H2A in DNA repair [J].
Downs, JA ;
Lowndes, NF ;
Jackson, SP .
NATURE, 2000, 408 (6815) :1001-1004
[9]   Yeast Rtt109 promotes genome stability by acetylating histone H3 on lysine 56 [J].
Driscoll, Robert ;
Hudson, Amanda ;
Jackson, Stephen P. .
SCIENCE, 2007, 315 (5812) :649-652
[10]   The processing of double-strand breaks and binding of single-strand-binding proteins RPA and Rad51 modulate the formation of ATR-kinase foci in yeast [J].
Dubrana, Karine ;
van Attikum, Haico ;
Hediger, Florence ;
Gasser, Susan M. .
JOURNAL OF CELL SCIENCE, 2007, 120 (23) :4209-4220