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Discovery of the major 15–30 nt mammalian small RNAs, their biogenesis and function
Small RNAs (sRNAs) within 15-30 nt such as miRNA, tsRNA, srRNA with 3’-OH have been identified. However, whether these sRNAs are the major 15-30 nt sRNAs is still unknown. Here we show about 90% mammalian sRNAs within 15-30 nt end with 2’,3’-cyclic phosphate (3’-cP). TANT-seq was developed to simult...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10507107/ https://www.ncbi.nlm.nih.gov/pubmed/37723159 http://dx.doi.org/10.1038/s41467-023-41554-6 |
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author | Lai, Hejin Feng, Ning Zhai, Qiwei |
author_facet | Lai, Hejin Feng, Ning Zhai, Qiwei |
author_sort | Lai, Hejin |
collection | PubMed |
description | Small RNAs (sRNAs) within 15-30 nt such as miRNA, tsRNA, srRNA with 3’-OH have been identified. However, whether these sRNAs are the major 15-30 nt sRNAs is still unknown. Here we show about 90% mammalian sRNAs within 15-30 nt end with 2’,3’-cyclic phosphate (3’-cP). TANT-seq was developed to simultaneously profile sRNAs with 3’-cP (sRNA-cPs) and sRNA-OHs, and huge amount of sRNA-cPs were detected. Surprisingly, sRNA-cPs and sRNA-OHs usually have distinct sequences. The data from TANT-seq were validated by a novel method termed TE-qPCR, and Northern blot. Furthermore, we found that Angiogenin and RNase 4 contribute to the biogenesis of sRNA-cPs. Moreover, much more sRNA-cPs than sRNA-OHs bind to Ago2, and can regulate gene expression. Particularly, snR-2-cP regulates Bcl2 by targeting to its 3’UTR dependent on Ago2, and subsequently regulates apoptosis. In addition, sRNA-cPs can guide the cleavage of target RNAs in Ago2 complex as miRNAs without the requirement of 3’-cP. Our discovery greatly expands the repertoire of mammalian sRNAs, and provides strategies and powerful tools towards further investigation of sRNA-cPs. |
format | Online Article Text |
id | pubmed-10507107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105071072023-09-20 Discovery of the major 15–30 nt mammalian small RNAs, their biogenesis and function Lai, Hejin Feng, Ning Zhai, Qiwei Nat Commun Article Small RNAs (sRNAs) within 15-30 nt such as miRNA, tsRNA, srRNA with 3’-OH have been identified. However, whether these sRNAs are the major 15-30 nt sRNAs is still unknown. Here we show about 90% mammalian sRNAs within 15-30 nt end with 2’,3’-cyclic phosphate (3’-cP). TANT-seq was developed to simultaneously profile sRNAs with 3’-cP (sRNA-cPs) and sRNA-OHs, and huge amount of sRNA-cPs were detected. Surprisingly, sRNA-cPs and sRNA-OHs usually have distinct sequences. The data from TANT-seq were validated by a novel method termed TE-qPCR, and Northern blot. Furthermore, we found that Angiogenin and RNase 4 contribute to the biogenesis of sRNA-cPs. Moreover, much more sRNA-cPs than sRNA-OHs bind to Ago2, and can regulate gene expression. Particularly, snR-2-cP regulates Bcl2 by targeting to its 3’UTR dependent on Ago2, and subsequently regulates apoptosis. In addition, sRNA-cPs can guide the cleavage of target RNAs in Ago2 complex as miRNAs without the requirement of 3’-cP. Our discovery greatly expands the repertoire of mammalian sRNAs, and provides strategies and powerful tools towards further investigation of sRNA-cPs. Nature Publishing Group UK 2023-09-18 /pmc/articles/PMC10507107/ /pubmed/37723159 http://dx.doi.org/10.1038/s41467-023-41554-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Lai, Hejin Feng, Ning Zhai, Qiwei Discovery of the major 15–30 nt mammalian small RNAs, their biogenesis and function |
title | Discovery of the major 15–30 nt mammalian small RNAs, their biogenesis and function |
title_full | Discovery of the major 15–30 nt mammalian small RNAs, their biogenesis and function |
title_fullStr | Discovery of the major 15–30 nt mammalian small RNAs, their biogenesis and function |
title_full_unstemmed | Discovery of the major 15–30 nt mammalian small RNAs, their biogenesis and function |
title_short | Discovery of the major 15–30 nt mammalian small RNAs, their biogenesis and function |
title_sort | discovery of the major 15–30 nt mammalian small rnas, their biogenesis and function |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10507107/ https://www.ncbi.nlm.nih.gov/pubmed/37723159 http://dx.doi.org/10.1038/s41467-023-41554-6 |
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