Genes enriched in A/T-ending codons are co-regulated and conserved across mammals.

IF 9 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Cell Systems Pub Date : 2023-04-19 DOI:10.1016/j.cels.2023.02.002
Hannah Benisty, Xavier Hernandez-Alias, Marc Weber, Miquel Anglada-Girotto, Federica Mantica, Leandro Radusky, Gökçe Senger, Ferriol Calvet, Donate Weghorn, Manuel Irimia, Martin H Schaefer, Luis Serrano
{"title":"Genes enriched in A/T-ending codons are co-regulated and conserved across mammals.","authors":"Hannah Benisty,&nbsp;Xavier Hernandez-Alias,&nbsp;Marc Weber,&nbsp;Miquel Anglada-Girotto,&nbsp;Federica Mantica,&nbsp;Leandro Radusky,&nbsp;Gökçe Senger,&nbsp;Ferriol Calvet,&nbsp;Donate Weghorn,&nbsp;Manuel Irimia,&nbsp;Martin H Schaefer,&nbsp;Luis Serrano","doi":"10.1016/j.cels.2023.02.002","DOIUrl":null,"url":null,"abstract":"<p><p>Codon usage influences gene expression distinctly depending on the cell context. Yet, the importance of codon bias in the simultaneous turnover of specific groups of protein-coding genes remains to be investigated. Here, we find that genes enriched in A/T-ending codons are expressed more coordinately in general and across tissues and development than those enriched in G/C-ending codons. tRNA abundance measurements indicate that this coordination is linked to the expression changes of tRNA isoacceptors reading A/T-ending codons. Genes with similar codon composition are more likely to be part of the same protein complex, especially for genes with A/T-ending codons. The codon preferences of genes with A/T-ending codons are conserved among mammals and other vertebrates. We suggest that this orchestration contributes to tissue-specific and ontogenetic-specific expression, which can facilitate, for instance, timely protein complex formation.</p>","PeriodicalId":54348,"journal":{"name":"Cell Systems","volume":"14 4","pages":"312-323.e3"},"PeriodicalIF":9.0000,"publicationDate":"2023-04-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell Systems","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.cels.2023.02.002","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 3

Abstract

Codon usage influences gene expression distinctly depending on the cell context. Yet, the importance of codon bias in the simultaneous turnover of specific groups of protein-coding genes remains to be investigated. Here, we find that genes enriched in A/T-ending codons are expressed more coordinately in general and across tissues and development than those enriched in G/C-ending codons. tRNA abundance measurements indicate that this coordination is linked to the expression changes of tRNA isoacceptors reading A/T-ending codons. Genes with similar codon composition are more likely to be part of the same protein complex, especially for genes with A/T-ending codons. The codon preferences of genes with A/T-ending codons are conserved among mammals and other vertebrates. We suggest that this orchestration contributes to tissue-specific and ontogenetic-specific expression, which can facilitate, for instance, timely protein complex formation.

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
富含A/ t末端密码子的基因在哺乳动物中是共同调控和保守的。
密码子的使用对基因表达的影响取决于细胞环境。然而,密码子偏置在蛋白质编码基因的特定组同时更新中的重要性仍有待研究。本研究发现,与G/ c末端密码子富集的基因相比,A/ t末端密码子富集的基因在整个组织和发育过程中的表达更加协调。tRNA丰度测量表明,这种协调与读取A/ t端密码子的tRNA同工受体的表达变化有关。具有相似密码子组成的基因更有可能是相同蛋白质复合体的一部分,特别是对于具有A/ t结尾密码子的基因。A/ t端密码子基因的密码子偏好在哺乳动物和其他脊椎动物中是保守的。我们认为这种协调有助于组织特异性和个体特异性表达,例如,它可以促进及时的蛋白质复合物形成。
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
Cell Systems
Cell Systems Medicine-Pathology and Forensic Medicine
CiteScore
16.50
自引率
1.10%
发文量
84
审稿时长
42 days
期刊介绍: In 2015, Cell Systems was founded as a platform within Cell Press to showcase innovative research in systems biology. Our primary goal is to investigate complex biological phenomena that cannot be simply explained by basic mathematical principles. While the physical sciences have long successfully tackled such challenges, we have discovered that our most impactful publications often employ quantitative, inference-based methodologies borrowed from the fields of physics, engineering, mathematics, and computer science. We are committed to providing a home for elegant research that addresses fundamental questions in systems biology.
期刊最新文献
pH and buffering capacity: Fundamental yet underappreciated drivers of algal-bacterial interactions What’s driving rhythmic gene expression: Sleep or the clock? Model integration of circadian- and sleep-wake-driven contributions to rhythmic gene expression reveals distinct regulatory principles On knowing a gene: A distributional hypothesis of gene function Acute response to pathogens in the early human placenta at single-cell resolution
×
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