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小干扰 RNA 靶向与染色质相关的 RNA 诱导其在人细胞中的转录沉默。

Small Interfering RNAs Targeting a Chromatin-Associated RNA Induce Its Transcriptional Silencing in Human Cells.

机构信息

Molecular, Cellular and Developmental Biology Unit, Centre de Biologie Integrative, University of Toulouse, Université Paul Sabatier, CNRS, Toulouse, France.

Equipe labellisée Ligue Contre le Cancer, Toulouse, France.

出版信息

Mol Cell Biol. 2022 Dec 15;42(12):e0027122. doi: 10.1128/mcb.00271-22. Epub 2022 Nov 29.

Abstract

Transcriptional gene silencing by small interfering RNAs (siRNAs) has been widely described in various species, including plants and yeast. In mammals, its extent remains somewhat debated. Previous studies showed that siRNAs targeting gene promoters could induce the silencing of the targeted promoter, although the involvement of off-target mechanisms was also suggested. Here, by using nascent RNA capture and RNA polymerase II chromatin immunoprecipitation, we show that siRNAs targeting a chromatin-associated noncoding RNA induced its transcriptional silencing. Deletion of the sequence targeted by one of these siRNAs on the two alleles by genome editing further showed that this silencing was due to base-pairing of the siRNA to the target. Moreover, by using cells with heterozygous deletion of the target sequence, we showed that only the wild-type allele, but not the deleted allele, was silenced by the siRNA, indicating that transcriptional silencing occurred only in . Finally, we demonstrated that both Ago1 and Ago2 are involved in this transcriptional silencing. Altogether, our data demonstrate that siRNAs targeting a chromatin-associated RNA at a distance from its promoter induce its transcriptional silencing. Our results thus extend the possible repertoire of endogenous or exogenous interfering RNAs.

摘要

小干扰 RNA(siRNA)的转录基因沉默已在包括植物和酵母在内的各种物种中得到广泛描述。在哺乳动物中,其程度仍存在一些争议。先前的研究表明,针对基因启动子的 siRNA 可以诱导靶向启动子的沉默,尽管也提出了非靶向机制的参与。在这里,我们通过使用新生 RNA 捕获和 RNA 聚合酶 II 染色质免疫沉淀,表明靶向染色质相关非编码 RNA 的 siRNA 诱导了其转录沉默。通过基因组编辑删除这些 siRNA 靶向的两个等位基因中的一个序列,进一步表明这种沉默是由于 siRNA 与靶序列的碱基配对。此外,通过使用杂合缺失靶序列的细胞,我们表明只有野生型等位基因而非缺失等位基因被 siRNA 沉默,表明转录沉默仅发生在 。最后,我们证明 Ago1 和 Ago2 都参与了这种转录沉默。总的来说,我们的数据表明,靶向启动子较远的染色质相关 RNA 的 siRNA 诱导其转录沉默。因此,我们的结果扩展了内源性或外源性干扰 RNA 的可能范围。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fb4/9753735/a1af312f711b/mcb.00271-22-f001.jpg

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