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Splicing Factors Facilitate Rnai-directed Silencing In Fission Yeast

机译:剪接因子促进裂变酵母中Rnai定向沉默。

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Heterochromatin formation at fission yeast centromeres is directed by RNA interference (RNAi). Noncoding transcripts derived from centromeric repeats are processed into small interfering RNAs (siRNAs) that direct the RNA-induced transcriptional silencing (R1TS) effector complex to engage centromere transcripts, resulting in recruitment of the histone H3 lysine 9 methyltransferase Clr4, and hence silencing. We have found that defects in specific splicing factors, but not splicing itself, affect the generation of centromeric siRNAs and consequently centromeric heterochromatin integrity. Moreover, splicing factors physically associate with Cidl2, a component of the RNAi machinery, and with centromeric chromatin, consistent with a direct role in RNAi. We propose that spliceosomal complexes provide a platform for siRNA generation and hence facilitate effective centromere repeat silencing.
机译:裂变酵母着丝粒处异染色质的形成受RNA干扰(RNAi)的控制。源自着丝粒重复序列的非编码转录本被加工成小的干扰RNA(siRNA),该RNA指导RNA诱导的转录沉默(R1TS)效应子复合体与着丝粒转录本接合,从而导致组蛋白H3赖氨酸9甲基转移酶Clr4募集并因此沉默。我们已经发现特定剪接因子中的缺陷(而不是自身剪接)会影响着丝粒siRNA的生成,从而影响着丝粒异染色质的完整性。此外,剪接因子与RNAi机器的组成部分Cidl2和与着丝粒染色质物理相关,这与RNAi的直接作用一致。我们建议剪接体复合物提供了一个平台,用于siRNA的产生,从而促进有效的着丝粒重复沉默。

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