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保守的RNA结合亲环蛋白Rct1独立于异染色质组装调控小RNA生物合成和剪接。

The Conserved RNA Binding Cyclophilin, Rct1, Regulates Small RNA Biogenesis and Splicing Independent of Heterochromatin Assembly.

作者信息

Chang An-Yun, Castel Stephane E, Ernst Evan, Kim Hyun Soo, Martienssen Robert A

机构信息

Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA; Molecular and Cellular Biology Program, Stony Brook University, Stony Brook, NY 11794, USA.

Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA; Watson School of Biological Sciences, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA.

出版信息

Cell Rep. 2017 Jun 20;19(12):2477-2489. doi: 10.1016/j.celrep.2017.05.086.

Abstract

RNAi factors and their catalytic activities are essential for heterochromatin assembly in S. pombe. This has led to the idea that siRNAs can promote H3K9 methylation by recruiting the cryptic loci regulator complex (CLRC), also known as recombination in K complex (RIKC), to the nucleation site. The conserved RNA-binding protein Rct1 (AtCyp59/SIG-7) interacts with splicing factors and RNA polymerase II. Here we show that Rct1 promotes processing of pericentromeric transcripts into siRNAs via the RNA recognition motif. Surprisingly, loss of siRNA in rct1 mutants has no effect on H3K9 di- or tri-methylation, resembling other splicing mutants, suggesting that post-transcriptional gene silencing per se is not required to maintain heterochromatin. Splicing of the Argonaute gene is also defective in rct1 mutants and contributes to loss of silencing but not to loss of siRNA. Our results suggest that Rct1 guides transcripts to the RNAi machinery by promoting splicing of elongating non-coding transcripts.

摘要

RNA干扰因子及其催化活性对于粟酒裂殖酵母中的异染色质组装至关重要。这引发了一种观点,即小干扰RNA(siRNA)可通过将隐匿位点调节复合物(CLRC,也称为K复合物中的重组(RIKC))招募到成核位点来促进组蛋白H3赖氨酸9(H3K9)甲基化。保守的RNA结合蛋白Rct1(AtCyp59/SIG-7)与剪接因子和RNA聚合酶II相互作用。在此我们表明,Rct1通过RNA识别基序促进着丝粒周围转录本加工成siRNA。令人惊讶的是,rct1突变体中siRNA的缺失对H3K9二甲基化或三甲基化没有影响,这与其他剪接突变体相似,表明维持异染色质本身并不需要转录后基因沉默。Argonaute基因的剪接在rct1突变体中也存在缺陷,并且导致沉默丧失,但不导致siRNA丧失。我们的结果表明,Rct1通过促进延伸的非编码转录本的剪接将转录本引导至RNA干扰机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e18/5600480/e232340164ad/nihms884876f1.jpg

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