RAD53, DUN1 and PDS1 define two parallel G2/M checkpoint pathways in budding yeast

被引:142
作者
Gardner, R [1 ]
Putnam, CW [1 ]
Weinert, T [1 ]
机构
[1] Univ Arizona, Dept Mol & Cellular Biol, Tucson, AZ 85721 USA
关键词
checkpoint; DNA damage; mitotic arrest; Pds1; Rad53;
D O I
10.1093/emboj/18.11.3173
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
Eukaryotic checkpoint genes regulate multiple cellular responses to DNA damage. In this report, we examine the roles of budding yeast genes involved in G(2)/M arrest and tolerance to UV exposure. A current model posits three gene classes: those encoding proteins acting on damaged DNA (e.g. RAD9 and RAD24), those transducing a signal (MEC1, RAD53 and DUN1) or those participating more directly in arrest (PDS1), Here, we define important features of the pathways subserved by those genes. MEC1, which we find is required for both establishment and maintenance of G(2)/M arrest, mediates this arrest through two parallel pathways. One pathway requires RAD53 and DUN1 (the 'RAD53 pathway'); the other pathway requires PDS1, Each pathway independently contributes similar to 50% to G(2)/M arrest, effects demonstrable after cdc13-induced damage or a double-stranded break inflicted by the HO endonuclease, Similarly, both pathways contribute independently to tolerance of UV irradiation. How the parallel pathways might interact ultimately to achieve arrest is not yet understood, but we do provide evidence that neither the RAD53 nor the PDS1 pathway appears to maintain arrest by inhibiting adaptation. Instead, we think it likely that both pathways contribute to establishing and maintaining arrest.
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页码:3173 / 3185
页数:13
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