Department of Biochemistry, University of Oxford, Oxford OX1 3QU, UK.
School of Biosciences, College of Life & Environmental Sciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.
Cell Rep. 2021 Sep 7;36(10):109671. doi: 10.1016/j.celrep.2021.109671.
Phosphorylation of the RNA polymerase II C-terminal domain YSPTSPS consensus sequence coordinates key events during transcription, and its deregulation leads to defects in transcription and RNA processing. Here, we report that the histone deacetylase activity of the fission yeast Hos2/Set3 complex plays an important role in suppressing cryptic initiation of antisense transcription when RNA polymerase II phosphorylation is dysregulated due to the loss of Ssu72 phosphatase. Interestingly, although single Hos2 and Set3 mutants have little effect, loss of Hos2 or Set3 combined with ssu72Δ results in a synergistic increase in antisense transcription globally and correlates with elevated sensitivity to genotoxic agents. We demonstrate a key role for the Ssu72/Hos2/Set3 mechanism in the suppression of cryptic antisense transcription at the 3' end of convergent genes that are most susceptible to these defects, ensuring the fidelity of gene expression within dense genomes of simple eukaryotes.
RNA 聚合酶 II C 末端结构域 YSPTSPS 共有序列的磷酸化协调转录过程中的关键事件,其失调会导致转录和 RNA 加工缺陷。在这里,我们报告说裂殖酵母 Hos2/Set3 复合物的组蛋白去乙酰化酶活性在 RNA 聚合酶 II 磷酸化因 Ssu72 磷酸酶缺失而失调时,对抑制反义转录的隐性起始起着重要作用。有趣的是,尽管单个 Hos2 和 Set3 突变体的影响很小,但 Hos2 或 Set3 的缺失与 ssu72Δ 的组合导致反义转录在全局上协同增加,并与对遗传毒性药物的敏感性增加相关。我们证明了 Ssu72/Hos2/Set3 机制在抑制最易受这些缺陷影响的会聚基因 3'端隐性反义转录中的关键作用,确保了在简单真核生物密集基因组中基因表达的保真度。