The replication stress response is an essential pathway that deals with the obstacles that halt the progression of DNA replication forks even during an unperturbed S phase. Basal activation of the ATR and CHK1 kinases prevents the premature firing of origins of replication during S phase, avoiding the activation of an excessive number of replication forks and the appearance of genomic instability. However, the mechanisms that regulate ATR activation in the unperturbed S phase have not been fully determined. Here we present evidence that the AAA ATPase VCP/p97 regulates the presence of the DNA polymerase α/Primase complex (POLA/PRIM) on chromatin, thus limiting its activity and hampering the subsequent activation of ATR by TOPBP1. As a consequence, inhibiting VCP/p97 activates ATR and CHK1 and leads to a cell cycle arrest in G2/M. We propose that the priming activity of POLA/PRIM in the lagging strand is one of the determinants of the basal activation of ATR during an unperturbed S phase and VCP/p97 limits this activation through the extraction of POLA/PRIM from chromatin.
DNA polymerase α/primase extraction from chromatin by VCP/p97 restricts ATR activation during unperturbed DNA replication.
VCP/p97 从染色质中提取 DNA 聚合酶 α/引物酶,限制了未受干扰的 DNA 复制过程中 ATR 的激活
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作者:RodrÃguez-Acebes Sara, MartÃn-Rufo Rodrigo, Gómez-Moya Alicia, Churcher Scott B, Fernández-Llorente Alejandro, de la Vega-Barranco Guillermo, Perona Alejandra, Oroz Pilar, MartÃn-Doncel Elena, Toledo Luis Ignacio, Méndez Juan, Lecona Emilio
| 期刊: | Nature Communications | 影响因子: | 15.700 |
| 时间: | 2025 | 起止号: | 2025 Jul 1; 16(1):5706 |
| doi: | 10.1038/s41467-025-60077-w | 研究方向: | 其它 |
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