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PP2C磷酸酶Ptc2和Ptc3是双链断裂后DNA检查点失活所必需的。

PP2C phosphatases Ptc2 and Ptc3 are required for DNA checkpoint inactivation after a double-strand break.

作者信息

Leroy Christophe, Lee Sang Eun, Vaze Moreshwar B, Ochsenbein Françoise, Guerois Raphaël, Haber James E, Marsolier-Kergoat Marie-Claude

机构信息

Service de Biochimie et de Génétique Moléculaire, CEA/Saclay, 91191 Gif-sur-Yvette, Cedex, France.

出版信息

Mol Cell. 2003 Mar;11(3):827-35. doi: 10.1016/s1097-2765(03)00058-3.

Abstract

Saccharomyces cells suffering a DNA double-strand break (DSB) ultimately escape checkpoint-mediated G2/M arrest either by recovery once the lesion is repaired or by adaptation if the lesion proves irreparable. Cells lacking the PP2C-like phosphatases Ptc2 and Ptc3 are unable to adapt to a HO-induced DSB and are also defective in recovering from a repairable DSB. In contrast, overexpression of PTC2 rescues adaptation-defective yku80Delta and cdc5-ad mutants. These effects are not explained by alterations either in the processing of DSB ends or in DSB repair. In vivo and in vitro evidence suggests that phosphorylated forms of Ptc2 and Ptc3 specifically bind to the Rad53 FHA1 domain and inactivate Rad53-dependent pathways during adaptation and recovery by dephosphorylating Rad53.

摘要

遭受DNA双链断裂(DSB)的酿酒酵母细胞最终通过损伤修复后的恢复或在损伤无法修复时通过适应来逃避检查点介导的G2/M期阻滞。缺乏PP2C样磷酸酶Ptc2和Ptc3的细胞无法适应HO诱导的DSB,并且在从可修复的DSB中恢复方面也存在缺陷。相比之下,PTC2的过表达挽救了适应缺陷型的yku80Delta和cdc5 - ad突变体。这些效应无法通过DSB末端处理或DSB修复的改变来解释。体内和体外证据表明,Ptc2和Ptc3的磷酸化形式特异性结合到Rad53 FHA1结构域,并在适应和恢复过程中通过使Rad53去磷酸化来使依赖Rad53的途径失活。

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