首页> 外文期刊>Genes and Development: a Journal Devoted to the Molecular Analysis of Gene Expression in Eukaryotes, Prokaryotes, and Viruses >Piwi induces piRNA-guided transcriptional silencing and establishment of a repressive chromatin state
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Piwi induces piRNA-guided transcriptional silencing and establishment of a repressive chromatin state

机译:Piwi诱导piRNA指导的转录沉默和抑制性染色质状态的建立

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In the metazoan germline, piwi proteins and associated piwi-interacting RNAs (piRNAs) provide a defense system against the expression of transposable elements. In the cytoplasm, piRNA sequences guide piwi complexes to destroy complementary transposon transcripts by endonucleolytic cleavage. However, some piwi family members are nuclear, raising the possibility of alternative pathways for piRNA-mediated regulation of gene expression. We found that Drosophila Piwi is recruited to chromatin, colocalizing with RNA polymerase II (Pol II) on polytene chromosomes. Knockdown of Piwi in the germline increases expression of transposable elements that are targeted by piRNAs, whereas protein-coding genes remain largely unaffected. Derepression of transposons upon Piwi depletion correlates with increased occupancy of Pol II on their promoters. Expression of piRNAs that target a reporter construct results in a decrease in Pol II occupancy and an increase in repressive H3K9me3 marks and heterochromatin protein 1 (HP1) on the reporter locus. Our results indicate that Piwi identifies targets complementary to the associated piRNA and induces transcriptional repression by establishing a repressive chromatin state when correct targets are found. ? 2013 by Cold Spring Harbor Laboratory Press.
机译:在后生种系中,piwi蛋白和相关的piwi相互作用RNA(piRNA)提供了防御转座因子表达的防御系统。在细胞质中,piRNA序列指导piwi复合物通过内切核酸酶裂解破坏互补的转座子转录物。但是,一些piwi家族成员是有核的,从而增加了piRNA介导的基因表达调控的替代途径的可能性。我们发现果蝇Piwi被征募到染色质,与polytene染色体上的RNA聚合酶II(Pol II)共定位。在种系中敲除Piwi可以增加piRNA靶向的转座因子的表达,而蛋白质编码基因在很大程度上不受影响。 Piwi耗竭后转座子的阻遏与其启动子上Pol II的占用增加有关。靶向报道基因构建体的piRNA的表达导致报道基因座上Pol II占有率的降低以及抑制性H3K9me3标记和异染色质蛋白1(HP1)的增加。我们的结果表明,Piwi可识别与相关piRNA互补的靶标,并在发现正确的靶标时通过建立抑制性染色质状态来诱导转录抑制。 ? 2013年,冷泉港实验室出版社。

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