Advanced Research Facilities & Services, Preeminent Medical Photonics Education & Research Center, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka 431-3192, Japan.
Department of Molecular Biology, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka 431-3192, Japan.
Biochim Biophys Acta Mol Cell Res. 2023 Aug;1870(6):119484. doi: 10.1016/j.bbamcr.2023.119484. Epub 2023 May 17.
Ataxia-telangiectasia mutated and Rad3-related (ATR) kinase is a crucial regulator of the cell cycle checkpoint and activated in response to DNA replication stress by two independent pathways via RPA32-ETAA1 and TopBP1. However, the precise activation mechanism of ATR by the RPA32-ETAA1 pathway remains unclear. Here, we show that p130RB2, a member of the retinoblastoma protein family, participates in the pathway under hydroxyurea-induced DNA replication stress. p130RB2 binds to ETAA1, but not TopBP1, and depletion of p130RB2 inhibits the RPA32-ETAA1 interaction under replication stress. Moreover, p130RB2 depletion reduces ATR activation accompanied by phosphorylation of its targets RPA32, Chk1, and ATR itself. It also causes improper re-progression of S phase with retaining single-stranded DNA after cancelation of the stress, which leads to an increase in the anaphase bridge phenotype and a decrease in cell survival. Importantly, restoration of p130RB2 rescued the disrupted phenotypes of p130RB2 knockdown cells. These results suggest positive involvement of p130RB2 in the RPA32-ETAA1-ATR axis and proper re-progression of the cell cycle to maintain genome integrity.
共济失调毛细血管扩张突变和 Rad3 相关(ATR)激酶是细胞周期检查点的关键调节剂,通过 RPA32-ETAA1 和 TopBP1 这两条独立的途径对 DNA 复制应激激活。然而,ATR 通过 RPA32-ETAA1 途径的精确激活机制尚不清楚。在这里,我们表明视网膜母细胞瘤蛋白家族的成员 p130RB2 在羟基脲诱导的 DNA 复制应激下参与该途径。p130RB2 与 ETAA1 结合,但不与 TopBP1 结合,并且在复制应激下耗尽 p130RB2 会抑制 RPA32-ETAA1 相互作用。此外,p130RB2 耗竭会减少 ATR 的激活,同时伴随着其靶标 RPA32、Chk1 和 ATR 自身的磷酸化。它还会导致 S 期的不正确再进展,在应激消除后保留单链 DNA,从而导致后期桥联表型增加和细胞存活减少。重要的是,p130RB2 的恢复挽救了 p130RB2 敲低细胞的破坏表型。这些结果表明 p130RB2 积极参与 RPA32-ETAA1-ATR 轴和细胞周期的适当再进展,以维持基因组完整性。