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Post-transcriptional repression of CFP-1 expands the regulatory repertoire of LIN-41/TRIM71
The Caenorhabditis elegans LIN-41/TRIM71 is a well-studied example of a versatile regulator of mRNA fate, which plays different biological functions involving distinct post-transcriptional mechanisms. In the soma, LIN-41 determines the timing of developmental transitions between larval stages. The s...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10602926/ https://www.ncbi.nlm.nih.gov/pubmed/37670562 http://dx.doi.org/10.1093/nar/gkad729 |
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author | Kumari, Pooja Thuestad, Lars Harald Ciosk, Rafal |
author_facet | Kumari, Pooja Thuestad, Lars Harald Ciosk, Rafal |
author_sort | Kumari, Pooja |
collection | PubMed |
description | The Caenorhabditis elegans LIN-41/TRIM71 is a well-studied example of a versatile regulator of mRNA fate, which plays different biological functions involving distinct post-transcriptional mechanisms. In the soma, LIN-41 determines the timing of developmental transitions between larval stages. The somatic LIN-41 recognizes specific mRNAs via LREs (LIN-41 Recognition Elements) and elicits either mRNA decay or translational repression. In the germline, LIN-41 controls the oocyte-to-embryo transition (OET), although the relevant targets and regulatory mechanisms are poorly understood. The germline LIN-41 was suggested to regulate mRNAs indirectly by associating with another RNA-binding protein. We show here that LIN-41 can also regulate germline mRNAs via the LREs. Through a computational-experimental analysis, we identified the germline mRNAs potentially controlled via LREs and validated one target, the cfp-1 mRNA, encoding a conserved chromatin modifier. Our analysis suggests that cfp-1 may be a long-sought target whose LIN-41-mediated regulation during OET facilitates the transcriptional reprogramming underlying the switch from germ- to somatic cell identity. |
format | Online Article Text |
id | pubmed-10602926 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-106029262023-10-28 Post-transcriptional repression of CFP-1 expands the regulatory repertoire of LIN-41/TRIM71 Kumari, Pooja Thuestad, Lars Harald Ciosk, Rafal Nucleic Acids Res RNA and RNA-protein complexes The Caenorhabditis elegans LIN-41/TRIM71 is a well-studied example of a versatile regulator of mRNA fate, which plays different biological functions involving distinct post-transcriptional mechanisms. In the soma, LIN-41 determines the timing of developmental transitions between larval stages. The somatic LIN-41 recognizes specific mRNAs via LREs (LIN-41 Recognition Elements) and elicits either mRNA decay or translational repression. In the germline, LIN-41 controls the oocyte-to-embryo transition (OET), although the relevant targets and regulatory mechanisms are poorly understood. The germline LIN-41 was suggested to regulate mRNAs indirectly by associating with another RNA-binding protein. We show here that LIN-41 can also regulate germline mRNAs via the LREs. Through a computational-experimental analysis, we identified the germline mRNAs potentially controlled via LREs and validated one target, the cfp-1 mRNA, encoding a conserved chromatin modifier. Our analysis suggests that cfp-1 may be a long-sought target whose LIN-41-mediated regulation during OET facilitates the transcriptional reprogramming underlying the switch from germ- to somatic cell identity. Oxford University Press 2023-09-06 /pmc/articles/PMC10602926/ /pubmed/37670562 http://dx.doi.org/10.1093/nar/gkad729 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | RNA and RNA-protein complexes Kumari, Pooja Thuestad, Lars Harald Ciosk, Rafal Post-transcriptional repression of CFP-1 expands the regulatory repertoire of LIN-41/TRIM71 |
title | Post-transcriptional repression of CFP-1 expands the regulatory repertoire of LIN-41/TRIM71 |
title_full | Post-transcriptional repression of CFP-1 expands the regulatory repertoire of LIN-41/TRIM71 |
title_fullStr | Post-transcriptional repression of CFP-1 expands the regulatory repertoire of LIN-41/TRIM71 |
title_full_unstemmed | Post-transcriptional repression of CFP-1 expands the regulatory repertoire of LIN-41/TRIM71 |
title_short | Post-transcriptional repression of CFP-1 expands the regulatory repertoire of LIN-41/TRIM71 |
title_sort | post-transcriptional repression of cfp-1 expands the regulatory repertoire of lin-41/trim71 |
topic | RNA and RNA-protein complexes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10602926/ https://www.ncbi.nlm.nih.gov/pubmed/37670562 http://dx.doi.org/10.1093/nar/gkad729 |
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