The structural determinants of checkpoint activation

被引:177
作者
MacDougall, Christina A. [1 ]
Byun, Tony S. [1 ]
Van, Christopher [1 ]
Yee, Muh-ching [1 ]
Cimprich, Karlene A. [1 ]
机构
[1] Stanford Univ, Dept Chem & Syst Biol, Stanford, CA 94305 USA
关键词
ATR; checkpoint; Xenopus; ssDNA; primed ssDNA; replication;
D O I
10.1101/gad.1522607
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Here, we demonstrate that primed, single-stranded DNA (ssDNA) is sufficient for activation of the ATR-dependent checkpoint pathway in Xenopus egg extracts. Using this structure, we define the contribution of the 5'- and 3'-primer ends to Chk1 activation when replication is blocked and ongoing. In addition, we show that although ssDNA is not sufficient for checkpoint activation, the amount of ssDNA adjacent to the primer influences the level of Chk1 phosphorylation. These observations define the minimal DNA requirements for checkpoint activation and suggest that primed ssDNA represents a common checkpoint activating-structure formed following many types of damage.
引用
收藏
页码:898 / 903
页数:6
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