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mRNA 结构决定了假尿嘧啶核苷合成酶 1 的修饰。

mRNA structure determines modification by pseudouridine synthase 1.

机构信息

Department of Biology, Massachusetts Institute of Technology, Cambridge, MA, USA.

Biogen, Cambridge, MA, USA.

出版信息

Nat Chem Biol. 2019 Oct;15(10):966-974. doi: 10.1038/s41589-019-0353-z. Epub 2019 Sep 2.

Abstract

Pseudouridine (Ψ) is a post-transcriptional RNA modification that alters RNA-RNA and RNA-protein interactions that affect gene expression. Messenger RNA pseudouridylation was recently discovered as a widespread and conserved phenomenon, but the mechanisms responsible for selective, regulated pseudouridylation of specific sequences within mRNAs were unknown. Here, we have revealed mRNA targets for five pseudouridine synthases and probed the determinants of mRNA target recognition by the predominant mRNA pseudouridylating enzyme, Pus1, by developing high-throughput kinetic analysis of pseudouridylation in vitro. Combining computational prediction and rational mutational analysis revealed an RNA structural motif that is both necessary and sufficient for mRNA pseudouridylation. Applying this structural context information predicted hundreds of additional mRNA targets that were pseudouridylated in vivo. These results demonstrate a structure-dependent mode of mRNA target recognition by a conserved pseudouridine synthase and implicate modulation of RNA structure as the probable mechanism to regulate mRNA pseudouridylation.

摘要

假尿嘧啶核苷(Ψ)是一种转录后 RNA 修饰,可改变 RNA-RNA 和 RNA-蛋白质相互作用,从而影响基因表达。信使 RNA 假尿嘧啶核苷酰化最近被发现是一种广泛存在且保守的现象,但负责在 mRNAs 内特定序列中选择性、调节假尿嘧啶核苷酰化的机制尚不清楚。在这里,我们揭示了五个假尿嘧啶核苷合成酶的 mRNA 靶标,并通过开发体外假尿嘧啶化的高通量动力学分析,探测主要的 mRNA 假尿嘧啶化酶 Pus1 对 mRNA 靶标识别的决定因素。结合计算预测和合理的突变分析,揭示了一个既必要又充分的 mRNA 假尿嘧啶化的 RNA 结构基序。应用这种结构上下文信息预测了数百个其他在体内被假尿嘧啶化的 mRNA 靶标。这些结果表明,保守的假尿嘧啶核苷合成酶以依赖结构的方式识别 mRNA 靶标,并暗示调节 RNA 结构可能是调节 mRNA 假尿嘧啶化的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8344/6764900/b200472aa61f/nihms-1535497-f0001.jpg

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