核糖核酸识别的最小ProQ脑膜炎奈瑟菌。

IF 5 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY RNA Pub Date : 2025-03-18 DOI:10.1261/rna.080207.124
Maciej Basczok, Mikołaj Olejniczak
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引用次数: 0

摘要

脑膜炎奈瑟菌最小ProQ是一种全局RNA结合蛋白,属于fino结构域蛋白家族。脑膜炎奈索菌ProQ仅由FinO结构域和短的N端和c端延伸组成。为了更好地理解这种最小的fino结构域蛋白是如何识别RNA的,我们比较了它与该蛋白的七种不同天然RNA配体的结合。接下来,其中两种rna, rpmG-3'和AniS,进行了进一步的突变研究。结果表明,脑膜炎奈瑟菌ProQ与内在转录终止子发夹下部结合,终止子茎5′和3′侧的单链序列是紧密结合所必需的。然而,两种RNA之间最佳结合所需的5‘和3’ RNA序列的特定长度不同。此外,我们的数据显示,3‘端核糖的2’-OH和3'-OH基团有助于脑膜炎奈瑟菌ProQ的RNA结合。综上所述,来自脑膜炎奈瑟菌的最小ProQ蛋白对RNA结合的要求与该家族其他蛋白分离的FinO结构域大致相似,但在详细的RNA特征上与它们不同,这些特征对于特异性RNA识别是最佳的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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RNA recognition by minimal ProQ from Neisseria meningitidis.

Neisseria meningitidis minimal ProQ is a global RNA-binding protein belonging to the family of FinO-domain proteins. The N. meningitidis ProQ consists only of the FinO domain accompanied by short N- and C-terminal extensions. To better understand how this minimal FinO-domain protein recognizes RNAs, we compared its binding to seven different natural RNA ligands of this protein. Next, two of these RNAs, rpmG-3' and AniS, were subject to further mutational studies. The data showed that N. meningitidis ProQ binds the lower part of the intrinsic transcription terminator hairpin, and that the single-stranded sequences on the 5' and 3' side of the terminator stem are required for tight binding. However, the specific lengths of 5' and 3' RNA sequences required for optimal binding differed between the two RNAs. Additionally, our data show that the 2'-OH and 3'-OH groups of the 3' terminal ribose contribute to RNA binding by N. meningitidis ProQ. In summary, the minimal ProQ protein from N. meningitidis has generally similar requirements for RNA binding as the isolated FinO domains of other proteins of this family, but differs from them in detailed RNA features that are optimal for specific RNA recognition.

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来源期刊
RNA
RNA 生物-生化与分子生物学
CiteScore
8.30
自引率
2.20%
发文量
101
审稿时长
2.6 months
期刊介绍: RNA is a monthly journal which provides rapid publication of significant original research in all areas of RNA structure and function in eukaryotic, prokaryotic, and viral systems. It covers a broad range of subjects in RNA research, including: structural analysis by biochemical or biophysical means; mRNA structure, function and biogenesis; alternative processing: cis-acting elements and trans-acting factors; ribosome structure and function; translational control; RNA catalysis; tRNA structure, function, biogenesis and identity; RNA editing; rRNA structure, function and biogenesis; RNA transport and localization; regulatory RNAs; large and small RNP structure, function and biogenesis; viral RNA metabolism; RNA stability and turnover; in vitro evolution; and RNA chemistry.
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