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Translation and codon usage regulate Argonaute slicer activity to trigger small RNA biogenesis
In the Caenorhabditis elegans germline, thousands of mRNAs are concomitantly expressed with antisense 22G-RNAs, which are loaded into the Argonaute CSR-1. Despite their essential functions for animal fertility and embryonic development, how CSR-1 22G-RNAs are produced remains unknown. Here, we show...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8190271/ https://www.ncbi.nlm.nih.gov/pubmed/34108460 http://dx.doi.org/10.1038/s41467-021-23615-w |
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author | Singh, Meetali Cornes, Eric Li, Blaise Quarato, Piergiuseppe Bourdon, Loan Dingli, Florent Loew, Damarys Proccacia, Simone Cecere, Germano |
author_facet | Singh, Meetali Cornes, Eric Li, Blaise Quarato, Piergiuseppe Bourdon, Loan Dingli, Florent Loew, Damarys Proccacia, Simone Cecere, Germano |
author_sort | Singh, Meetali |
collection | PubMed |
description | In the Caenorhabditis elegans germline, thousands of mRNAs are concomitantly expressed with antisense 22G-RNAs, which are loaded into the Argonaute CSR-1. Despite their essential functions for animal fertility and embryonic development, how CSR-1 22G-RNAs are produced remains unknown. Here, we show that CSR-1 slicer activity is primarily involved in triggering the synthesis of small RNAs on the coding sequences of germline mRNAs and post-transcriptionally regulates a fraction of targets. CSR-1-cleaved mRNAs prime the RNA-dependent RNA polymerase, EGO-1, to synthesize 22G-RNAs in phase with translating ribosomes, in contrast to other 22G-RNAs mostly synthesized in germ granules. Moreover, codon optimality and efficient translation antagonize CSR-1 slicing and 22G-RNAs biogenesis. We propose that codon usage differences encoded into mRNA sequences might be a conserved strategy in eukaryotes to regulate small RNA biogenesis and Argonaute targeting. |
format | Online Article Text |
id | pubmed-8190271 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81902712021-07-01 Translation and codon usage regulate Argonaute slicer activity to trigger small RNA biogenesis Singh, Meetali Cornes, Eric Li, Blaise Quarato, Piergiuseppe Bourdon, Loan Dingli, Florent Loew, Damarys Proccacia, Simone Cecere, Germano Nat Commun Article In the Caenorhabditis elegans germline, thousands of mRNAs are concomitantly expressed with antisense 22G-RNAs, which are loaded into the Argonaute CSR-1. Despite their essential functions for animal fertility and embryonic development, how CSR-1 22G-RNAs are produced remains unknown. Here, we show that CSR-1 slicer activity is primarily involved in triggering the synthesis of small RNAs on the coding sequences of germline mRNAs and post-transcriptionally regulates a fraction of targets. CSR-1-cleaved mRNAs prime the RNA-dependent RNA polymerase, EGO-1, to synthesize 22G-RNAs in phase with translating ribosomes, in contrast to other 22G-RNAs mostly synthesized in germ granules. Moreover, codon optimality and efficient translation antagonize CSR-1 slicing and 22G-RNAs biogenesis. We propose that codon usage differences encoded into mRNA sequences might be a conserved strategy in eukaryotes to regulate small RNA biogenesis and Argonaute targeting. Nature Publishing Group UK 2021-06-09 /pmc/articles/PMC8190271/ /pubmed/34108460 http://dx.doi.org/10.1038/s41467-021-23615-w Text en © The Author(s) 2021 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 Singh, Meetali Cornes, Eric Li, Blaise Quarato, Piergiuseppe Bourdon, Loan Dingli, Florent Loew, Damarys Proccacia, Simone Cecere, Germano Translation and codon usage regulate Argonaute slicer activity to trigger small RNA biogenesis |
title | Translation and codon usage regulate Argonaute slicer activity to trigger small RNA biogenesis |
title_full | Translation and codon usage regulate Argonaute slicer activity to trigger small RNA biogenesis |
title_fullStr | Translation and codon usage regulate Argonaute slicer activity to trigger small RNA biogenesis |
title_full_unstemmed | Translation and codon usage regulate Argonaute slicer activity to trigger small RNA biogenesis |
title_short | Translation and codon usage regulate Argonaute slicer activity to trigger small RNA biogenesis |
title_sort | translation and codon usage regulate argonaute slicer activity to trigger small rna biogenesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8190271/ https://www.ncbi.nlm.nih.gov/pubmed/34108460 http://dx.doi.org/10.1038/s41467-021-23615-w |
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