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假尿嘧啶核苷或如何利用微弱的能量差异。

Pseudouridines or how to draw on weak energy differences.

机构信息

Architecture et Réactivité de l'ARN, Université de Strasbourg, Institut de Biologie Moléculaire et Cellulaire du CNRS, 15 rue René Descartes, 67084, Strasbourg, France.

出版信息

Biochem Biophys Res Commun. 2019 Dec 17;520(4):702-704. doi: 10.1016/j.bbrc.2019.10.009.

DOI:10.1016/j.bbrc.2019.10.009
PMID:31761086
Abstract

In many RNA molecules, pseudouridines occur at conserved positions in functional sites. A great diversity of pseudouridine synthases guarantees the insertion of the modified base at precise locations. The accepted structural role of pseudouridines is a reduction of the RNA flexibility around the modification site. However, experiments rarely yield clear-cut evidence. The article "Dynamic stacking of an expected branch point adenosine in duplexes containing pseudouridine-modified or unmodified U2 snRNA sites" published in 2019 in Biochemical and Biophysical Research Communication by Kennedy et al. constitute a provocative case [1]. This example illustrates how a definite conformational state can be selected through small energy differences in a constrained environment.

摘要

在许多 RNA 分子中,假尿嘧啶核苷出现在功能位点的保守位置。大量的假尿嘧啶核苷合酶保证了修饰碱基精确地插入到特定位置。假尿嘧啶核苷被认为可以降低修饰位点附近 RNA 的灵活性。然而,实验很少能提供明确的证据。Kennedy 等人于 2019 年在《生物化学与生物物理研究通讯》发表的文章“含假尿嘧啶核苷修饰或未修饰 U2 snRNA 位点的双链体中预期分支点腺苷的动态堆积”[1]就是一个有启发性的例子。这个例子说明了在受限环境中,通过微小的能量差异如何选择确定的构象状态。

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1
Pseudouridines or how to draw on weak energy differences.假尿嘧啶核苷或如何利用微弱的能量差异。
Biochem Biophys Res Commun. 2019 Dec 17;520(4):702-704. doi: 10.1016/j.bbrc.2019.10.009.
2
Dynamic stacking of an expected branch point adenosine in duplexes containing pseudouridine-modified or unmodified U2 snRNA sites.含有假尿嘧啶核苷修饰或未修饰 U2 snRNA 位点的双链体中预期分支点腺苷的动态堆积。
Biochem Biophys Res Commun. 2019 Apr 2;511(2):416-421. doi: 10.1016/j.bbrc.2019.02.073. Epub 2019 Feb 21.
3
X-ray structures of U2 snRNA-branchpoint duplexes containing conserved pseudouridines.含有保守假尿苷的U2小核仁核糖核酸-分支点双链体的X射线结构
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A conserved pseudouridine modification in eukaryotic U2 snRNA induces a change in branch-site architecture.真核生物U2小核RNA中一种保守的假尿苷修饰会导致分支位点结构发生变化。
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Functions and mechanisms of spliceosomal small nuclear RNA pseudouridylation.剪接体小核 RNA 假尿嘧啶化的功能和机制。
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Modification of human U4 RNA requires U6 RNA and multiple pseudouridine synthases.人类U4 RNA的修饰需要U6 RNA和多种假尿苷合成酶。
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Sculpting of the spliceosomal branch site recognition motif by a conserved pseudouridine.由保守的假尿苷对剪接体分支位点识别基序进行塑造。
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Pseudouridines in and near the branch site recognition region of U2 snRNA are required for snRNP biogenesis and pre-mRNA splicing in Xenopus oocytes.非洲爪蟾卵母细胞中,U2 snRNA分支位点识别区域及其附近的假尿苷对于snRNP生物合成和前体mRNA剪接是必需的。
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Recognition of the spliceosomal branch site RNA helix on the basis of surface and electrostatic features.基于表面和静电特征识别剪接体分支位点RNA螺旋结构
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Biochemistry. 1991 Feb 19;30(7):1795-801. doi: 10.1021/bi00221a010.

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