Phosphoregulation of the checkpoint kinase Mec1ATR

被引:2
|
作者
Yates, Luke A. [1 ,2 ]
Zhang, Xiaodong [1 ,2 ]
机构
[1] Imperial Coll London, Dept Infect Dis, Sect Struct, Sir Alexander Fleming Bldg, London SW7 2AZ, England
[2] Francis Crick Inst, DNA Proc machines Lab, London NW1 1AT, England
基金
英国惠康基金;
关键词
DNA damage; DNA repair; DNA replication; Kinase; Checkpoint; Cell Cycle; DNA-DAMAGE CHECKPOINT; REPLICATION PROTEIN-A; S-PHASE CHECKPOINT; BUDDING YEAST; FHA DOMAIN; STRUCTURAL BASIS; GLOBAL ANALYSIS; SITE CLUSTERS; END RESECTION; HISTONE H2A;
D O I
10.1016/j.dnarep.2023.103543
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Yeast Mec1, and its mammalian ortholog, Ataxia-Telangiectasia and Rad3-related, are giant protein kinases central to replication stress and double strand DNA break repair. Mec1ATR, in complex with Ddc2ATRIP, is a 'sensor' of single stranded DNA, and phosphorylates numerous cell cycle and DNA repair factors to enforce cell cycle arrest and facilitate repair. Over the last several years, new techniques - particularly in structural biology - have provided molecular mechanisms for Mec1ATR function. It is becoming increasingly clear how post -translational modification of Mec1ATR and its interaction partners modulates the DNA damage checkpoint. In this review, we summarise the most recent work unravelling Mec1ATR function in the DNA damage checkpoint and provide a molecular context for its regulation by phosphorylation.
引用
收藏
页数:14
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