Identification of leader-trailer helices of precursor ribosomal RNA in all phyla of bacteria and archaea.

IF 4.2 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY RNA Pub Date : 2024-09-16 DOI:10.1261/rna.080091.124
Bryan T Gemler, Benjamin R Warner, Ralf Bundschuh, Kurt Fredrick
{"title":"Identification of leader-trailer helices of precursor ribosomal RNA in all phyla of bacteria and archaea.","authors":"Bryan T Gemler, Benjamin R Warner, Ralf Bundschuh, Kurt Fredrick","doi":"10.1261/rna.080091.124","DOIUrl":null,"url":null,"abstract":"<p><p>Ribosomal RNAs are transcribed as part of larger precursor molecules. In <i>Escherichia coli</i>, complementary RNA segments flank each rRNA and form long leader-trailer (LT) helices, which are crucial for subunit biogenesis in the cell. A previous study of 15 representative species suggested that most but not all prokaryotes contain LT helices. Here, we use a combination of in silico folding and covariation methods to identify and characterize LT helices in 4464 bacterial and 260 archaeal organisms. Our results suggest that LT helices are present in all phyla, including Deinococcota, which had previously been suspected to lack LT helices. In very few organisms, our pipeline failed to detect LT helices for both 16S and 23S rRNA. However, a closer case-by-case look revealed that LT helices are indeed present but escaped initial detection. Over 3600 secondary structure models, many well supported by nucleotide covariation, were generated. These structures show a high degree of diversity. Yet, all exhibit extensive base-pairing between the leader and trailer strands, in line with a common and essential function.</p>","PeriodicalId":21401,"journal":{"name":"RNA","volume":" ","pages":"1264-1276"},"PeriodicalIF":4.2000,"publicationDate":"2024-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11404451/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"RNA","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1261/rna.080091.124","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Ribosomal RNAs are transcribed as part of larger precursor molecules. In Escherichia coli, complementary RNA segments flank each rRNA and form long leader-trailer (LT) helices, which are crucial for subunit biogenesis in the cell. A previous study of 15 representative species suggested that most but not all prokaryotes contain LT helices. Here, we use a combination of in silico folding and covariation methods to identify and characterize LT helices in 4464 bacterial and 260 archaeal organisms. Our results suggest that LT helices are present in all phyla, including Deinococcota, which had previously been suspected to lack LT helices. In very few organisms, our pipeline failed to detect LT helices for both 16S and 23S rRNA. However, a closer case-by-case look revealed that LT helices are indeed present but escaped initial detection. Over 3600 secondary structure models, many well supported by nucleotide covariation, were generated. These structures show a high degree of diversity. Yet, all exhibit extensive base-pairing between the leader and trailer strands, in line with a common and essential function.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
鉴定所有细菌和古细菌门中核糖体前体 RNA 的领导-拖曳螺旋。
核糖体 RNA 是作为较大前体分子的一部分转录的。在大肠杆菌中,每个 rRNA 侧面都有互补的 RNA 片段,并形成长的领导-拖尾(LT)螺旋,这对细胞中亚基的生物生成至关重要。之前对 15 个代表性物种的研究表明,大多数原核生物都含有 LT 螺旋,但并非所有原核生物都是如此。在这里,我们结合使用了硅学折叠和共变方法,对 4464 种细菌和 260 种古生物中的 LT 螺旋进行了鉴定和表征。我们的研究结果表明,LT螺旋存在于所有门类中,包括之前被怀疑缺乏LT螺旋的Deinococcota。在极少数生物中,我们的分析管道未能检测到 16S 和 23S rRNA 的 LT 螺旋。然而,通过逐一仔细观察,我们发现LT螺旋确实存在,但却没有被检测到。我们生成了 3,618 个二级结构模型,其中许多都得到了核苷酸共变的有力支持。这些结构显示出高度的多样性。然而,所有这些结构都显示了领导链和引导链之间广泛的碱基配对,这与共同的基本功能是一致的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
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.
期刊最新文献
Mitochondrial mRNA and the Small Subunit rRNA in Budding Yeasts Undergo 3'-End Processing at Conserved Species-specific Elements. Independent neofunctionalization of Dxo1 in Saccharomyces and Candida led to 25S rRNA processing function. Sod1-deficient cells are impaired in formation of the modified nucleosides mcm5s2U and yW in tRNA. Beyond RNA-binding domains: determinants of protein-RNA binding. Identification, characterization, and structure of a tRNA splicing enzyme RNA 5'-OH kinase from the pathogenic fungi Mucorales.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1