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 (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, 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.

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Publication Details

Journal
Cell
Published
2024-11-22
DOI
https://doi.org/10.1016/j.cell.2024.10.046
Citations
44
Primary Topic
RNA and protein synthesis mechanisms
Type
article
Field-Weighted Citation Impact
10.29
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snoRNA-facilitated protein secretion revealed by transcriptome-wide snoRNA target identification

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snoRNA-facilitated protein secretion revealed by transcriptome-wide snoRNA target identification

Marta Majcherska-Agrawal, Tao Pan, Tong Wu, Tie-Bo Zeng, Fei Ji, Bernadette A. Miao, Yuhao Zhong, Pingluan Wang, Robert J. Keenan, Chuan He, Shun Liu, Bei Liu, Arunkumar Sundaram, Yutao Zhao
article en
44 citations

Abstract

Small nucleolar RNAs (snoRNAs) are non-coding RNAs known for guiding RNA modifications, including 2'-O-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, 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.

CellVol. 188(2)
University of Chicago (US)
Zero hunger
Openalex Percentile: Top 1%
RNA and protein synthesis mechanisms
10.29
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