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Hrp3 controls nucleosome positioning to suppress non-coding transcription in eu- and heterochromatin

机译:Hrp3控制核小体定位以抑制eu-和异染色质中的非编码转录

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摘要

The positioning of the nucleosome by ATP-dependent remodellers provides the fundamental chromatin environment for the regulation of diverse cellular processes acting on the underlying DNA. Recently, genome-wide nucleosome mapping has revealed more detailed information on the chromatin-remodelling factors. Here, we report that the Schizosaccharomyces pombe CHD remodeller, Hrp3, is a global regulator that drives proper nucleosome positioning and nucleosome stability. The loss of Hrp3 resulted in nucleosome perturbation across the chromosome, and the production of antisense transcripts in the hrp3Δ cells emphasized the importance of nucleosome architecture for proper transcription. Notably, perturbation of the nucleosome in hrp3 deletion mutant was also associated with destabilization of the DNA–histone interaction and cell cycle-dependent alleviation of heterochromatin silencing. Furthermore, the effect of Hrp3 in the pericentric region was found to be accomplished via a physical interaction with Swi6, and appeared to cooperate with other heterochromatin factors for gene silencing. Taken together, our data indicate that a well-positioned nucleosome by Hrp3 is important for the spatial-temporal control of transcription-associated processes.
机译:ATP依赖的重塑剂对核小体的定位为调节作用于基础DNA的各种细胞过程提供了基本的染色质环境。最近,全基因组的核小体作图揭示了有关染色质重塑因子的更多详细信息。在这里,我们报告粟酒裂殖酵母冠心病重塑,Hrp3,是驱动适当的核小体定位和核小体稳定性的全球监管机构。 Hrp3的丢失导致整个染色体上的核小体扰动,并且hrp3Δ细胞中反义转录物的产生强调了核小体结构对于正确转录的重要性。值得注意的是,hrp3缺失突变体中核小体的扰动还与DNA-组蛋白相互作用的失稳和异染色质沉默的细胞周期依赖性缓解有关。此外,发现Hrp3在外周中心区域的作用是通过与Swi6的物理相互作用来实现的,并且似乎与其他异染色质因子协同作用以实现基因沉默。综上所述,我们的数据表明,Hrp3定位良好的核小体对于转录相关过程的时空控制很重要。

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