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Mature mRNA processing that deletes 3′ end sequences directs translational activation and embryonic development
Eggs accumulate thousands of translationally repressed mRNAs that are translated into proteins after fertilization to direct diverse developmental processes. However, molecular mechanisms underlying the translation of stored mRNAs after fertilization remain unclear. Here, we report a previously unkn...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10672166/ https://www.ncbi.nlm.nih.gov/pubmed/38000026 http://dx.doi.org/10.1126/sciadv.adg6532 |
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author | Takada, Yuki Fierro, Ludivine Sato, Keisuke Sanada, Takahiro Ishii, Anna Yamamoto, Takehiro Kotani, Tomoya |
author_facet | Takada, Yuki Fierro, Ludivine Sato, Keisuke Sanada, Takahiro Ishii, Anna Yamamoto, Takehiro Kotani, Tomoya |
author_sort | Takada, Yuki |
collection | PubMed |
description | Eggs accumulate thousands of translationally repressed mRNAs that are translated into proteins after fertilization to direct diverse developmental processes. However, molecular mechanisms underlying the translation of stored mRNAs after fertilization remain unclear. Here, we report a previously unknown RNA processing of 3′ end sequences of mature mRNAs that activates the translation of stored mRNAs. Specifically, 9 to 72 nucleotides at the 3′ ends of zebrafish pou5f3 and mouse Pou5f1 mRNAs were deleted in the early stages of development. Reporter assays illustrated the effective translation of the truncated forms of mRNAs. Moreover, promotion and inhibition of the shortening of 3′ ends accelerated and attenuated Pou5f3 accumulation, respectively, resulting in defective development. Identification of proteins binding to unprocessed and/or processed mRNAs revealed that mRNA shortening acts as molecular switches. Comprehensive analysis revealed that >250 mRNAs underwent this processing. Therefore, our results provide a molecular principle that triggers the translational activation and directs development. |
format | Online Article Text |
id | pubmed-10672166 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-106721662023-11-24 Mature mRNA processing that deletes 3′ end sequences directs translational activation and embryonic development Takada, Yuki Fierro, Ludivine Sato, Keisuke Sanada, Takahiro Ishii, Anna Yamamoto, Takehiro Kotani, Tomoya Sci Adv Biomedicine and Life Sciences Eggs accumulate thousands of translationally repressed mRNAs that are translated into proteins after fertilization to direct diverse developmental processes. However, molecular mechanisms underlying the translation of stored mRNAs after fertilization remain unclear. Here, we report a previously unknown RNA processing of 3′ end sequences of mature mRNAs that activates the translation of stored mRNAs. Specifically, 9 to 72 nucleotides at the 3′ ends of zebrafish pou5f3 and mouse Pou5f1 mRNAs were deleted in the early stages of development. Reporter assays illustrated the effective translation of the truncated forms of mRNAs. Moreover, promotion and inhibition of the shortening of 3′ ends accelerated and attenuated Pou5f3 accumulation, respectively, resulting in defective development. Identification of proteins binding to unprocessed and/or processed mRNAs revealed that mRNA shortening acts as molecular switches. Comprehensive analysis revealed that >250 mRNAs underwent this processing. Therefore, our results provide a molecular principle that triggers the translational activation and directs development. American Association for the Advancement of Science 2023-11-24 /pmc/articles/PMC10672166/ /pubmed/38000026 http://dx.doi.org/10.1126/sciadv.adg6532 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Takada, Yuki Fierro, Ludivine Sato, Keisuke Sanada, Takahiro Ishii, Anna Yamamoto, Takehiro Kotani, Tomoya Mature mRNA processing that deletes 3′ end sequences directs translational activation and embryonic development |
title | Mature mRNA processing that deletes 3′ end sequences directs translational activation and embryonic development |
title_full | Mature mRNA processing that deletes 3′ end sequences directs translational activation and embryonic development |
title_fullStr | Mature mRNA processing that deletes 3′ end sequences directs translational activation and embryonic development |
title_full_unstemmed | Mature mRNA processing that deletes 3′ end sequences directs translational activation and embryonic development |
title_short | Mature mRNA processing that deletes 3′ end sequences directs translational activation and embryonic development |
title_sort | mature mrna processing that deletes 3′ end sequences directs translational activation and embryonic development |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10672166/ https://www.ncbi.nlm.nih.gov/pubmed/38000026 http://dx.doi.org/10.1126/sciadv.adg6532 |
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