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TENT2、TUT4 和 TUT7 选择性调节 miRNA 序列和丰度。

TENT2, TUT4, and TUT7 selectively regulate miRNA sequence and abundance.

机构信息

RNA Mediated Gene Regulation Section; RNA Biology Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, MD, 21702, USA.

School of Basic Medicine, Zhejiang Chinese Medical University, Hangzhou, 310053, China.

出版信息

Nat Commun. 2022 Sep 7;13(1):5260. doi: 10.1038/s41467-022-32969-8.

Abstract

TENTs generate miRNA isoforms by 3' tailing. However, little is known about how tailing regulates miRNA function. Here, we generate isogenic HEK293T cell lines in which TENT2, TUT4 and TUT7 are knocked out individually or in combination. Together with rescue experiments, we characterize TENT-specific effects by deep sequencing, Northern blot and in vitro assays. We find that 3' tailing is not random but highly specific. In addition to its known adenylation, TENT2 contributes to guanylation and uridylation on mature miRNAs. TUT4 uridylates most miRNAs whereas TUT7 is dispensable. Removing adenylation has a marginal impact on miRNA levels. By contrast, abolishing uridylation leads to dysregulation of a set of miRNAs. Besides let-7, miR-181b and miR-222 are negatively regulated by TUT4/7 via distinct mechanisms while the miR-888 cluster is upregulated specifically by TUT7. Our results uncover the selective actions of TENTs in generating 3' isomiRs and pave the way to investigate their functions.

摘要

TENTs 通过 3' 加尾产生 miRNA 异构体。然而,关于加尾如何调节 miRNA 功能的知之甚少。在这里,我们生成了 TENT2、TUT4 和 TUT7 单独或组合敲除的同基因 HEK293T 细胞系。通过深度测序、Northern blot 和体外测定,我们结合拯救实验,对 TENT 特异性效应进行了表征。我们发现 3' 加尾不是随机的,而是高度特异的。除了已知的腺苷酸化外,TENT2 还有助于成熟 miRNA 的鸟苷酸化和尿苷酸化。TUT4 尿苷酸化大多数 miRNA,而 TUT7 则可有可无。去除腺苷酸化对 miRNA 水平的影响微不足道。相比之下,消除尿苷酸化会导致一组 miRNA 的失调。除了 let-7,miR-181b 和 miR-222 被 TUT4/7 通过不同的机制负调控,而 miR-888 簇则被 TUT7 特异性上调。我们的结果揭示了 TENT 在产生 3' 同型异构体方面的选择性作用,并为研究它们的功能铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/073f/9452540/0c7a7d848294/41467_2022_32969_Fig1_HTML.jpg

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