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Transcription Promotes the Interaction of the FAcilitates Chromatin Transactions (FACT) Complex with Nucleosomes in Saccharomyces cerevisiae

机译:转录促进酿酒酵母与核小体的染色质交易(FACT)复杂的相互作用。

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摘要

The FACT (FAcilitates Chromatin Transactions) complex is a conserved complex that maintains chromatin structure on transcriptionally active genes. Consistent with this, FACT is enriched on highly expressed genes, but how it is targeted to these regions is unknown. In vitro, FACT binds destabilized nucleosomes, supporting the hypothesis that FACT is targeted to transcribed chromatin through recognition of RNA polymerase (RNAP)-disrupted nucleosomes. In this study, we used high-resolution analysis of FACT occupancy in Saccharomyces cerevisiae to test this hypothesis. We demonstrate that FACT interacts with nucleosomes in vivo and that its interaction with chromatin is dependent on transcription by any of the three RNAPs. Deep sequencing of micrococcal nuclease-resistant fragments shows that FACT-bound nucleosomes exhibit differing nuclease sensitivity compared to bulk chromatin, consistent with a modified nucleosome structure being the preferred ligand for this complex. Interestingly, a subset of FACT-bound nucleosomes may be “overlapping dinucleosomes,” in which one histone octamer invades the ∼147-bp territory normally occupied by the adjacent nucleosome. While the differing nuclease sensitivity of FACT-bound nucleosomes could also be explained by the demonstrated ability of FACT to alter nucleosome structure, transcription inhibition restores nuclease resistance, suggesting that it is not due to FACT interaction alone. Collectively, these results are consistent with a model in which FACT is targeted to transcribed genes through preferential interaction with RNAP-disrupted nucleosomes.
机译:FACT(促进染色质交易)复合体是一种保守的复合体,可在转录活性基因上维持染色质结构。与此相一致,FACT富含高表达基因,但如何靶向这些区域尚不清楚。在体外,FACT结合不稳定的核小体,支持以下假设:FACT通过识别RNA聚合酶(RNAP)破坏的核小体靶向转录的染色质。在这项研究中,我们使用了酿酒酵母中FACT占用的高分辨率分析来检验该假设。我们证明FACT在体内与核小体相互作用,并且其与染色质的相互作用取决于三个RNAP中任何一个的转录。对微球菌核酸酶抗性片段的深度测序表明,与本体染色质相比,结合FACT的核小体显示出不同的核酸酶敏感性,这与修饰的核小体结构是该复合物的优选配体一致。有趣的是,与FACT结合的核小体的一个子集可能是“重叠的二核小体”,其中一个组蛋白八聚体侵入通常被相邻核小体占据的147bp区域。尽管结合FACT的核小体对核酸酶的敏感性不同,也可以通过FACT改变核小体结构的能力来解释,但转录抑制可恢复核酸酶的抗性,这表明这并非仅由于FACT相互作用而引起。总的来说,这些结果与其中FACT通过与RNAP破坏的核小体的优先相互作用靶向转录的基因的模型一致。

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