Rodríguez-Acebes Sara, Martín-Rufo Rodrigo, Gómez-Moya Alicia, Churcher Scott B, Fernández-Llorente Alejandro, de la Vega-Barranco Guillermo, Perona Alejandra, Oroz Pilar, Martín-Doncel Elena, Toledo Luis Ignacio, Méndez Juan, Lecona Emilio
DNA Replication Group, Molecular Oncology Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Chromatin, Cancer and the Ubiquitin System lab, Centro de Biología Molecular Severo Ochoa (CBM) CSIC-Universidad Autónoma de Madrid, Department of Genome Dynamics and Function, Madrid, Spain.
Nat Commun. 2025 Jul 1;16(1):5706. doi: 10.1038/s41467-025-60077-w.
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.
复制应激反应是一条重要途径,可应对即使在未受干扰的S期也会阻碍DNA复制叉前进的障碍。ATR和CHK1激酶的基础激活可防止S期复制起点过早启动,避免过多复制叉激活以及基因组不稳定的出现。然而,在未受干扰的S期调节ATR激活的机制尚未完全明确。在此,我们提供证据表明,AAA型ATP酶VCP/p97调节染色质上DNA聚合酶α/引物酶复合物(POLA/PRIM)的存在,从而限制其活性,并阻碍随后TOPBP1对ATR的激活。因此,抑制VCP/p97会激活ATR和CHK1,并导致细胞周期在G2/M期停滞。我们提出,滞后链中POLA/PRIM的引发活性是未受干扰的S期ATR基础激活的决定因素之一,而VCP/p97通过从染色质中提取POLA/PRIM来限制这种激活。