CRUK and MRC Oxford Institute for Radiation Oncology, Old Road Campus Research Building, University of Oxford, Oxford OX3 7DQ, UK.
DNA Repair (Amst). 2022 Nov;119:103407. doi: 10.1016/j.dnarep.2022.103407. Epub 2022 Sep 16.
Histone Post-Translational Modifications (PTMs) play fundamental roles in mediating DNA-related processes such as transcription, replication and repair. The histone mark H3K36me3 and its associated methyltransferase SETD2 (Set2 in yeast) are archetypical in this regard, performing critical roles in each of these DNA transactions. Here, we present an overview of H3K36me3 regulation and the roles of its writers, readers and erasers in maintaining genome stability through facilitating DNA double-strand break (DSB) repair, checkpoint signalling and replication stress responses. Further, we consider how loss of SETD2 and H3K36me3, frequently observed in a number of different cancer types, can be specifically targeted in the clinic through exploiting loss of particular genome stability functions.
组蛋白翻译后修饰(PTMs)在介导与 DNA 相关的过程中发挥着重要作用,如转录、复制和修复。组蛋白标记 H3K36me3 及其相关的甲基转移酶 SETD2(酵母中的 Set2)在这方面具有代表性,在这些 DNA 转导中都发挥着关键作用。在这里,我们概述了 H3K36me3 的调控以及其写入器、读取器和橡皮擦在通过促进 DNA 双链断裂(DSB)修复、检查点信号和复制应激反应来维持基因组稳定性方面的作用。此外,我们还考虑了 SETD2 和 H3K36me3 的缺失如何通过利用特定基因组稳定性功能的缺失在临床上被靶向治疗。