Different RNA recognition by ProQ and FinO depends on the sequence surrounding intrinsic terminator hairpins.

IF 5 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY RNA Pub Date : 2025-04-16 DOI:10.1261/rna.080206.124
Maria D Mamońska, Maciej M Basczok, Ewa M Stein, Julia Kurzawska, Mikołaj Olejniczak
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Abstract

Escherichia coli ProQ and FinO proteins both have RNA-binding FinO domains, which bind to intrinsic transcription terminators, but each protein recognizes distinct RNAs. To explore how ProQ and FinO discriminate between RNAs, we transplanted sequences surrounding terminator hairpins between RNAs specific for each protein, and compared their binding to ProQ, the isolated FinO domain of ProQ (ProQNTD), and FinO. The results showed that the binding specificity of chimeric RNAs toward ProQ, ProQNTD, or FinO was determined by the origin of the transplanted sequence. Further analysis showed that the sequence surrounding the terminator hairpin, including a purine-purine mismatch, in natural RNA ligands of FinO and in chimeric RNAs, weakened their binding by ProQNTD Overall, our studies suggest that RNA sequence elements surrounding the intrinsic terminator hairpin contribute to the discrimination between RNAs by ProQ and FinO.

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ProQ和FinO识别RNA的不同取决于内在终止子发夹周围的序列。
大肠杆菌ProQ和FinO蛋白都具有rna结合的FinO结构域,这些结构域与内在转录终止子结合,但每种蛋白识别不同的rna。为了探索ProQ和FinO如何区分rna,我们在每种蛋白质的特异性rna之间移植了终止发夹周围的序列,并比较了它们与ProQ、ProQ分离的FinO结构域(ProQNTD)和FinO的结合。结果表明,嵌合rna对ProQ、ProQNTD和FinO的结合特异性取决于移植序列的起源。进一步分析表明,FinO的天然RNA配体和嵌合RNA中终止子发夹周围的序列(包括嘌呤-嘌呤错配)削弱了ProQNTD与它们的结合。总的来说,我们的研究表明,围绕内在终止子发夹的RNA序列元件有助于ProQ和FinO对RNA的区分。
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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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