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BACH1/FANCJ Acts with TopBP1 and Participates Early in DNA Replication Checkpoint Control
被引:121
|作者:
Gong, Zihua
[1
]
Kim, Ja-Eun
[2
]
Leung, Charles Chung Yun
[3
]
Glover, J. N. Mark
[3
]
Chen, Junjie
[1
]
机构:
[1] Univ Texas MD Anderson Canc Ctr, Dept Expt Radiat Oncol, Houston, TX 77030 USA
[2] Kyung Hee Univ, Sch Med, Dept Pharmacol, Seoul 130701, South Korea
[3] Univ Alberta, Dept Biochem, Edmonton, AB T6G 2H7, Canada
基金:
美国国家卫生研究院;
关键词:
FANCONI-ANEMIA;
S-PHASE;
CONTAINING PROTEIN;
GENOME INTEGRITY;
DAMAGE RESPONSE;
BUDDING YEAST;
BRCT DOMAIN;
ATR;
PHOSPHORYLATION;
BACH1;
D O I:
10.1016/j.molcel.2010.01.002
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:
Human TopBP1 plays a critical role in the control of DNA replication checkpoint. In this study, we report a specific interaction between TopBP1 and BACH1/ FANCJ, a DNA helicase involved in the repair of DNA crosslinks. The TopBP1/BACH1 interaction is mediated by the very C-terminal tandem BRCT domains of TopBP1 and S phase-specific phosphorylation of BACH1 at Thr 1133 site. Interestingly, we demonstrate that depletion of TopBP1 or BACH1 attenuates the loading of RPA on chromatin. Moreover, both TopBP1 and BACH1 are required for ATR-dependent phosphorylation events in response to replication stress. Taken together, our data suggest that BACH1 has an unexpected early role in replication checkpoint control. A specific interaction between TopBP1 and BACH1 is likely to be required for the extension of single-stranded DNA regions and RPA loading following replication stress, which is a prerequisite for the subsequent activation of replication checkpoint.
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页码:438 / 446
页数:9
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