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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...

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Autores principales: Takada, Yuki, Fierro, Ludivine, Sato, Keisuke, Sanada, Takahiro, Ishii, Anna, Yamamoto, Takehiro, Kotani, Tomoya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2023
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.
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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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