Department of Molecular Biology, The Scripps Research Institute, La Jolla, California, United States of America.
PLoS Genet. 2010 Jul 22;6(7):e1001032. doi: 10.1371/journal.pgen.1001032.
Schizosaccharomyces pombe Rad3 checkpoint kinase and its human ortholog ATR are essential for maintaining genome integrity in cells treated with genotoxins that damage DNA or arrest replication forks. Rad3 and ATR also function during unperturbed growth, although the events triggering their activation and their critical functions are largely unknown. Here, we use ChIP-on-chip analysis to map genomic loci decorated by phosphorylated histone H2A (gammaH2A), a Rad3 substrate that establishes a chromatin-based recruitment platform for Crb2 and Brc1 DNA repair/checkpoint proteins. Unexpectedly, gammaH2A marks a diverse array of genomic features during S-phase, including natural replication fork barriers and a fork breakage site, retrotransposons, heterochromatin in the centromeres and telomeres, and ribosomal RNA (rDNA) repeats. gammaH2A formation at the centromeres and telomeres is associated with heterochromatin establishment by Clr4 histone methyltransferase. We show that gammaH2A domains recruit Brc1, a factor involved in repair of damaged replication forks. Brc1 C-terminal BRCT domain binding to gammaH2A is crucial in the absence of Rqh1(Sgs1), a RecQ DNA helicase required for rDNA maintenance whose human homologs are mutated in patients with Werner, Bloom, and Rothmund-Thomson syndromes that are characterized by cancer-predisposition or accelerated aging. We conclude that Rad3 phosphorylates histone H2A to mobilize Brc1 to critical genomic domains during S-phase, and this pathway functions in parallel with Rqh1 DNA helicase in maintaining genome integrity.
裂殖酵母 Rad3 检查点激酶及其人类同源物 ATR 在受到破坏 DNA 或阻止复制叉的遗传毒物处理的细胞中维持基因组完整性方面是必不可少的。Rad3 和 ATR 也在未受干扰的生长过程中发挥作用,尽管触发它们激活的事件及其关键功能在很大程度上是未知的。在这里,我们使用 ChIP-on-chip 分析来绘制磷酸化组蛋白 H2A(gammaH2A)修饰的基因组位点,gammaH2A 是 Rad3 的底物,它建立了 Crb2 和 Brc1 等 DNA 修复/检查点蛋白的基于染色质的募集平台。出乎意料的是,gammaH2A 在 S 期标记了一系列不同的基因组特征,包括天然复制叉障碍和叉断裂位点、逆转录转座子、着丝粒和端粒中的异染色质以及核糖体 RNA(rDNA)重复序列。Clr4 组蛋白甲基转移酶参与异染色质的建立,导致着丝粒和端粒处形成 gammaH2A。我们表明,gammaH2A 结构域招募 Brc1,这是一种参与修复受损复制叉的因子。Brc1 C 末端 BRCT 结构域与 gammaH2A 的结合对于缺乏 Rqh1(Sgs1)至关重要,Rqh1(Sgs1)是一种 RecQ DNA 解旋酶,对于 rDNA 维持是必需的,其人类同源物在 Werner、Bloom 和 Rothmund-Thomson 综合征患者中发生突变,这些患者具有癌症易感性或加速衰老的特征。我们得出结论,Rad3 磷酸化组蛋白 H2A 以在 S 期将 Brc1 动员到关键基因组区域,并且该途径与 Rqh1 DNA 解旋酶平行发挥作用,以维持基因组完整性。