首页> 美国卫生研究院文献>The Journal of Biological Chemistry >Histone H3K56 Acetylation Is Required for Quelling-induced Small RNA Production through Its Role in Homologous Recombination
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Histone H3K56 Acetylation Is Required for Quelling-induced Small RNA Production through Its Role in Homologous Recombination

机译:组蛋白H3K56乙酰化是必需的通过其在同源重组中的作用来抑制诱导的小RNA产生。

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摘要

Quelling and DNA damage-induced small RNA (qiRNA) production are RNA interference (RNAi)-related phenomenon from repetitive genomic loci in Neurospora. We have recently proposed that homologous recombination from repetitive DNA loci allows the RNAi pathway to recognize repetitive DNA to produce small RNA. However, the mechanistic detail of this pathway remains largely unclear. By systematically screening the Neurospora knock-out library, we identified RTT109 as a novel component required for small RNA production. RTT109 is a histone acetyltransferase for histone H3 lysine 56 (H3K56) and H3K56 acetylation is essential for the small RNA biogenesis pathway. Furthermore, we showed that RTT109 is required for homologous recombination and H3K56Ac is enriched around double strand break, which overlaps with RAD51 binding. Taken together, our results suggest that H3K56 acetylation is required for small RNA production through its role in homologous recombination.
机译:抑制和DNA损伤诱导的小RNA(qiRNA)产生是Neurospora中重复性基因组位点与RNA干扰(RNAi)相关的现象。我们最近提出,来自重复DNA基因座的同源重组允许RNAi途径识别重复DNA以产生小RNA。但是,该途径的机械细节仍不清楚。通过系统地筛选Neurospora基因敲除文库,我们将RTT109鉴定为产生小RNA所需的新型组分。 RTT109是组蛋白H3赖氨酸56(H3K56)的组蛋白乙酰基转移酶,H3K56乙酰化对于小RNA生物发生途径至关重要。此外,我们表明RTT109是同源重组所必需的,并且H3K56Ac在双链断裂附近富集,与RAD51结合重叠。两者合计,我们的结果表明H3K56乙酰化是通过其在同源重组中的作用产生小RNA所必需的。

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