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组蛋白突变将 R 环形成与基因组不稳定性诱导分离。

Histone Mutants Separate R Loop Formation from Genome Instability Induction.

机构信息

Centro Andaluz de Biología Molecular y Medicina Regenerativa-CABIMER, Universidad de Sevilla-CSIC-Universidad Pablo de Olavide, Seville 41092, Spain.

Centro Andaluz de Biología Molecular y Medicina Regenerativa-CABIMER, Universidad de Sevilla-CSIC-Universidad Pablo de Olavide, Seville 41092, Spain.

出版信息

Mol Cell. 2017 Jun 1;66(5):597-609.e5. doi: 10.1016/j.molcel.2017.05.014.

Abstract

R loops have positive physiological roles, but they can also be deleterious by causing genome instability, and the mechanisms for this are unknown. Here we identified yeast histone H3 and H4 mutations that facilitate R loops but do not cause instability. R loops containing single-stranded DNA (ssDNA), versus RNA-DNA hybrids alone, were demonstrated using ssDNA-specific human AID and bisulfite. Notably, they are similar size regardless of whether or not they induce genome instability. Contrary to mutants causing R loop-mediated instability, these histone mutants do not accumulate H3 serine-10 phosphate (H3S10-P). We propose a two-step mechanism in which, first, an altered chromatin facilitates R loops, and second, chromatin is modified, including H3S10-P, as a requisite for compromising genome integrity. Consistently, these histone mutations suppress the high H3S10 phosphorylation and genomic instability of hpr1 and sen1 mutants. Therefore, contrary to what was previously believed, R loops do not cause genome instability by themselves.

摘要

R 环具有积极的生理作用,但它们也可能通过导致基因组不稳定而产生有害影响,其机制尚不清楚。在这里,我们鉴定了酵母组蛋白 H3 和 H4 的突变,这些突变促进了 R 环的形成,但不会导致不稳定。使用单链 DNA(ssDNA)特异性的人 AID 和亚硫酸氢盐证明了含有单链 DNA(ssDNA)的 R 环,而不是单独的 RNA-DNA 杂交体。值得注意的是,无论是否诱导基因组不稳定,它们的大小都相似。与导致 R 环介导的不稳定的突变体相反,这些组蛋白突变体不会积累 H3 丝氨酸-10 磷酸(H3S10-P)。我们提出了一个两步机制,首先,改变的染色质促进了 R 环的形成,其次,染色质被修饰,包括 H3S10-P,作为破坏基因组完整性的必要条件。一致地,这些组蛋白突变抑制了 hpr1 和 sen1 突变体的高 H3S10 磷酸化和基因组不稳定性。因此,与之前的观点相反,R 环本身并不会导致基因组不稳定。

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