Beckta Jason M, Dever Seth M, Gnawali Nisha, Khalil Ashraf, Sule Amrita, Golding Sarah E, Rosenberg Elizabeth, Narayanan Aarthi, Kehn-Hall Kylene, Xu Bo, Povirk Lawrence F, Valerie Kristoffer
Department of Radiation Oncology, Virginia Commonwealth University, Richmond, VA 23298, USA.
Department of Biochemistry and Molecular Biology, Virginia Commonwealth University, Richmond, VA 23298, USA.
Oncotarget. 2015 Sep 29;6(29):27674-87. doi: 10.18632/oncotarget.4876.
Mutations in the breast cancer susceptibility 1 (BRCA1) gene are catalysts for breast and ovarian cancers. Most mutations are associated with the BRCA1 N- and C-terminal domains linked to DNA double-strand break (DSB) repair. However, little is known about the role of the intervening serine-glutamine (SQ) - cluster in the DNA damage response beyond its importance in regulating cell cycle checkpoints. We show that serine-to-alanine alterations at critical residues within the SQ-cluster known to be phosphorylated by ATM and ATR result in reduced homologous recombination repair (HRR) and aberrant mitosis. While a S1387A BRCA1 mutant - previously shown to abrogate S-phase arrest in response to radiation - resulted in only a modest decrease in HRR, S1387A together with an additional alteration, S1423A (BRCA12P), reduced HRR to vector control levels and similar to a quadruple mutant also including S1457A and S1524A (BRCA14P). These effects appeared to be independent of PALB2. Furthermore, we found that BRCA14P promoted a prolonged and struggling HRR late in the cell cycle and shifted DSB repair from HRR to non-homologous end joining which, in the face of irreparable chromosomal damage, resulted in mitotic catastrophe. Altogether, SQ-cluster phosphorylation is critical for allowing adequate time for completing normal HRR prior to mitosis and preventing cells from entering G1 prematurely resulting in gross chromosomal aberrations.
乳腺癌易感基因1(BRCA1)的突变是乳腺癌和卵巢癌的催化剂。大多数突变与BRCA1的N端和C端结构域有关,这些结构域与DNA双链断裂(DSB)修复相关。然而,关于中间的丝氨酸 - 谷氨酰胺(SQ)簇在DNA损伤反应中的作用,除了其在调节细胞周期检查点中的重要性外,人们知之甚少。我们发现,已知被ATM和ATR磷酸化的SQ簇内关键残基的丝氨酸到丙氨酸的改变会导致同源重组修复(HRR)减少和有丝分裂异常。虽然先前已证明S1387A BRCA1突变体 - 可消除对辐射的S期阻滞 - 仅导致HRR适度下降,但S1387A与另一个改变S1423A(BRCA12P)一起,将HRR降低到载体对照水平,类似于还包括S1457A和S1524A的四重突变体(BRCA14P)。这些效应似乎与PALB2无关。此外,我们发现BRCA14P在细胞周期后期促进了长时间且艰难的HRR,并将DSB修复从HRR转变为非同源末端连接,面对无法修复的染色体损伤,这导致了有丝分裂灾难。总之,SQ簇磷酸化对于在有丝分裂之前留出足够时间完成正常HRR以及防止细胞过早进入G1期从而导致严重染色体畸变至关重要。