Bei Liu, Tong Wu, Bernadette A. Miao, Fei Ji, Shun Liu, Pingluan Wang, Yutao Zhao, Yuhao Zhong, Arunkumar Sundaram, Tie-Bo Zeng, Marta Majcherska-Agrawal, Robert J. Keenan, Tao Pan, Chuan He
{"title":"通过转录组范围内的 snoRNA 目标鉴定揭示 snoRNA 促进蛋白质分泌的作用","authors":"Bei Liu, Tong Wu, Bernadette A. Miao, Fei Ji, Shun Liu, Pingluan Wang, Yutao Zhao, Yuhao Zhong, Arunkumar Sundaram, Tie-Bo Zeng, Marta Majcherska-Agrawal, Robert J. Keenan, Tao Pan, Chuan He","doi":"10.1016/j.cell.2024.10.046","DOIUrl":null,"url":null,"abstract":"Small nucleolar RNAs (snoRNAs) are non-coding RNAs known for guiding RNA modifications, including 2′-<em>O</em>-methylation (N<sub>m</sub>) and pseudouridine (Ψ). While snoRNAs may also interact with other RNAs, such as mRNA, the full repertoire of RNAs targeted by snoRNA remains elusive due to the lack of effective technologies that identify snoRNA targets transcriptome wide. Here, we develop a chemical crosslinking-based approach that comprehensively detects cellular RNA targets of snoRNAs, yielding thousands of previously unrecognized snoRNA-mRNA interactions in human cells and mouse brain tissues. Many interactions occur outside of snoRNA-guided RNA modification sites, hinting at non-canonical functions beyond RNA modification. We find that one of these snoRNAs, <em>SNORA73</em>, targets mRNAs that encode secretory proteins and membrane proteins. <em>SNORA73</em> also interacts with <em>7SL</em> RNA, part of the signal recognition particle (SRP) required for protein secretion. The mRNA-<em>SNORA73</em>-<em>7SL</em> RNA interactions enhance the association of the <em>SNORA73</em>-target mRNAs with SRP, thereby facilitating the secretion of encoded proteins.","PeriodicalId":9656,"journal":{"name":"Cell","volume":"234 1","pages":""},"PeriodicalIF":45.5000,"publicationDate":"2024-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"snoRNA-facilitated protein secretion revealed by transcriptome-wide snoRNA target identification\",\"authors\":\"Bei Liu, Tong Wu, Bernadette A. Miao, Fei Ji, Shun Liu, Pingluan Wang, Yutao Zhao, Yuhao Zhong, Arunkumar Sundaram, Tie-Bo Zeng, Marta Majcherska-Agrawal, Robert J. Keenan, Tao Pan, Chuan He\",\"doi\":\"10.1016/j.cell.2024.10.046\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Small nucleolar RNAs (snoRNAs) are non-coding RNAs known for guiding RNA modifications, including 2′-<em>O</em>-methylation (N<sub>m</sub>) and pseudouridine (Ψ). While snoRNAs may also interact with other RNAs, such as mRNA, the full repertoire of RNAs targeted by snoRNA remains elusive due to the lack of effective technologies that identify snoRNA targets transcriptome wide. Here, we develop a chemical crosslinking-based approach that comprehensively detects cellular RNA targets of snoRNAs, yielding thousands of previously unrecognized snoRNA-mRNA interactions in human cells and mouse brain tissues. Many interactions occur outside of snoRNA-guided RNA modification sites, hinting at non-canonical functions beyond RNA modification. We find that one of these snoRNAs, <em>SNORA73</em>, targets mRNAs that encode secretory proteins and membrane proteins. <em>SNORA73</em> also interacts with <em>7SL</em> RNA, part of the signal recognition particle (SRP) required for protein secretion. The mRNA-<em>SNORA73</em>-<em>7SL</em> RNA interactions enhance the association of the <em>SNORA73</em>-target mRNAs with SRP, thereby facilitating the secretion of encoded proteins.\",\"PeriodicalId\":9656,\"journal\":{\"name\":\"Cell\",\"volume\":\"234 1\",\"pages\":\"\"},\"PeriodicalIF\":45.5000,\"publicationDate\":\"2024-11-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cell\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1016/j.cell.2024.10.046\",\"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}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.cell.2024.10.046","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}
snoRNA-facilitated protein secretion revealed by transcriptome-wide snoRNA target identification
Small nucleolar RNAs (snoRNAs) are non-coding RNAs known for guiding RNA modifications, including 2′-O-methylation (Nm) and pseudouridine (Ψ). While snoRNAs may also interact with other RNAs, such as mRNA, the full repertoire of RNAs targeted by snoRNA remains elusive due to the lack of effective technologies that identify snoRNA targets transcriptome wide. Here, we develop a chemical crosslinking-based approach that comprehensively detects cellular RNA targets of snoRNAs, yielding thousands of previously unrecognized snoRNA-mRNA interactions in human cells and mouse brain tissues. Many interactions occur outside of snoRNA-guided RNA modification sites, hinting at non-canonical functions beyond RNA modification. We find that one of these snoRNAs, SNORA73, targets mRNAs that encode secretory proteins and membrane proteins. SNORA73 also interacts with 7SL RNA, part of the signal recognition particle (SRP) required for protein secretion. The mRNA-SNORA73-7SL RNA interactions enhance the association of the SNORA73-target mRNAs with SRP, thereby facilitating the secretion of encoded proteins.
期刊介绍:
Cells is an international, peer-reviewed, open access journal that focuses on cell biology, molecular biology, and biophysics. It is affiliated with several societies, including the Spanish Society for Biochemistry and Molecular Biology (SEBBM), Nordic Autophagy Society (NAS), Spanish Society of Hematology and Hemotherapy (SEHH), and Society for Regenerative Medicine (Russian Federation) (RPO).
The journal publishes research findings of significant importance in various areas of experimental biology, such as cell biology, molecular biology, neuroscience, immunology, virology, microbiology, cancer, human genetics, systems biology, signaling, and disease mechanisms and therapeutics. The primary criterion for considering papers is whether the results contribute to significant conceptual advances or raise thought-provoking questions and hypotheses related to interesting and important biological inquiries.
In addition to primary research articles presented in four formats, Cells also features review and opinion articles in its "leading edge" section, discussing recent research advancements and topics of interest to its wide readership.