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Cell-cycle-specific activators of the Mec1/ATR checkpoint kinase
被引:24
|作者:
Navadgi-Patil, Vasundhara M.
[1
]
Burgers, Peter M.
[1
]
机构:
[1] Washington Univ, Sch Med, Dept Biochem & Mol Biophys, St Louis, MO 63110 USA
关键词:
ataxia telangiectasia mutated- and Rad3-related (ATR);
cell cycle;
checkpoint;
DNA damage;
DNA replication;
Mec1;
DNA-DAMAGE CHECKPOINT;
BUDDING YEAST;
SACCHAROMYCES-CEREVISIAE;
REPLICATION;
CLAMP;
PHOSPHORYLATION;
COMPLEXES;
ATR;
POLYMERASE;
HELICASE;
D O I:
10.1042/BST0390600
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:
Mec1 [ATR (ataxia telangiectasia mutated- and Rad3-related) in humans] is the principle kinase responsible for checkpoint activation in response to replication stress and DNA damage in Saccharomyces cerevisiae. The heterotrimeric checkpoint clamp, 9-1-1 (checkpoint clamp of Rad9, Rad1 and Hus1 in humans and Ddc1, Rad17 and Mec3 in S. cerevisiae; Ddc1-Mec3-Rad17) and the DNA replication initiation factor Dpb11 (human TopBP1) are the two known activators of Med. The 9-1-1 clamp functions in checkpoint activation in G(1) - and G(2)-phase, but its employment differs between these two phases of the cell cycle. The Ddc1 (human Rad9) subunit of the clamp directly activates Mec1 in G(1)-phase, an activity identified only in S. cerevisiae so far. However, in G(2)-phase, the 9-1-1 clamp activates the checkpoint by two mechanisms. One mechanism includes direct activation of Mec1 by the unstructured C-terminal tail of Odd. The second mechanism involves the recruitment of Dpb11 by the phosphorylated C-terminal tail of Ddc1. The latter mechanism is highly conserved and also functions in response to replication stress in higher eukaryotes. In S. cerevisiae, however, both the 9-1-1 clamp and the Dpb11 are partially redundant for checkpoint activation in response to replication stress, suggesting the existence of additional activators of Med.
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页码:600 / 605
页数:6
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