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RNA structural dynamics regulate early embryogenesis through controlling transcriptome fate and function
BACKGROUND: Vertebrate early embryogenesis is initially directed by a set of maternal RNAs and proteins, yet the mechanisms controlling this program remain largely unknown. Recent transcriptome-wide studies on RNA structure have revealed its pervasive and crucial roles in RNA processing and function...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7236375/ https://www.ncbi.nlm.nih.gov/pubmed/32423473 http://dx.doi.org/10.1186/s13059-020-02022-2 |
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author | Shi, Boyang Zhang, Jinsong Heng, Jian Gong, Jing Zhang, Ting Li, Pan Sun, Bao-Fa Yang, Ying Zhang, Ning Zhao, Yong-Liang Wang, Hai-Lin Liu, Feng Zhang, Qiangfeng Cliff Yang, Yun-Gui |
author_facet | Shi, Boyang Zhang, Jinsong Heng, Jian Gong, Jing Zhang, Ting Li, Pan Sun, Bao-Fa Yang, Ying Zhang, Ning Zhao, Yong-Liang Wang, Hai-Lin Liu, Feng Zhang, Qiangfeng Cliff Yang, Yun-Gui |
author_sort | Shi, Boyang |
collection | PubMed |
description | BACKGROUND: Vertebrate early embryogenesis is initially directed by a set of maternal RNAs and proteins, yet the mechanisms controlling this program remain largely unknown. Recent transcriptome-wide studies on RNA structure have revealed its pervasive and crucial roles in RNA processing and functions, but whether and how RNA structure regulates the fate of the maternal transcriptome have yet to be determined. RESULTS: Here we establish the global map of four nucleotide-based mRNA structures by icSHAPE during zebrafish early embryogenesis. Strikingly, we observe that RNA structurally variable regions are enriched in the 3′ UTR and contain cis-regulatory elements important for maternal-to-zygotic transition (MZT). We find that the RNA-binding protein Elavl1a stabilizes maternal mRNAs by binding to the cis-elements. Conversely, RNA structure formation suppresses Elavl1a’s binding leading to the decay of its maternal targets. CONCLUSIONS: Our study finds that RNA structurally variable regions are enriched in mRNA 3′ UTRs and contain cis-regulatory elements during zebrafish early embryogenesis. We reveal that Elavl1a regulates maternal RNA stability in an RNA structure-dependent fashion. Overall, our findings reveal a broad and fundamental role of RNA structure-based regulation in vertebrate early embryogenesis. ELECTRONIC SUPPLEMENTARY MATERIAL: Supplementary information accompanies this paper at 10.1186/s13059-020-02022-2. |
format | Online Article Text |
id | pubmed-7236375 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-72363752020-05-29 RNA structural dynamics regulate early embryogenesis through controlling transcriptome fate and function Shi, Boyang Zhang, Jinsong Heng, Jian Gong, Jing Zhang, Ting Li, Pan Sun, Bao-Fa Yang, Ying Zhang, Ning Zhao, Yong-Liang Wang, Hai-Lin Liu, Feng Zhang, Qiangfeng Cliff Yang, Yun-Gui Genome Biol Research BACKGROUND: Vertebrate early embryogenesis is initially directed by a set of maternal RNAs and proteins, yet the mechanisms controlling this program remain largely unknown. Recent transcriptome-wide studies on RNA structure have revealed its pervasive and crucial roles in RNA processing and functions, but whether and how RNA structure regulates the fate of the maternal transcriptome have yet to be determined. RESULTS: Here we establish the global map of four nucleotide-based mRNA structures by icSHAPE during zebrafish early embryogenesis. Strikingly, we observe that RNA structurally variable regions are enriched in the 3′ UTR and contain cis-regulatory elements important for maternal-to-zygotic transition (MZT). We find that the RNA-binding protein Elavl1a stabilizes maternal mRNAs by binding to the cis-elements. Conversely, RNA structure formation suppresses Elavl1a’s binding leading to the decay of its maternal targets. CONCLUSIONS: Our study finds that RNA structurally variable regions are enriched in mRNA 3′ UTRs and contain cis-regulatory elements during zebrafish early embryogenesis. We reveal that Elavl1a regulates maternal RNA stability in an RNA structure-dependent fashion. Overall, our findings reveal a broad and fundamental role of RNA structure-based regulation in vertebrate early embryogenesis. ELECTRONIC SUPPLEMENTARY MATERIAL: Supplementary information accompanies this paper at 10.1186/s13059-020-02022-2. BioMed Central 2020-05-18 /pmc/articles/PMC7236375/ /pubmed/32423473 http://dx.doi.org/10.1186/s13059-020-02022-2 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Shi, Boyang Zhang, Jinsong Heng, Jian Gong, Jing Zhang, Ting Li, Pan Sun, Bao-Fa Yang, Ying Zhang, Ning Zhao, Yong-Liang Wang, Hai-Lin Liu, Feng Zhang, Qiangfeng Cliff Yang, Yun-Gui RNA structural dynamics regulate early embryogenesis through controlling transcriptome fate and function |
title | RNA structural dynamics regulate early embryogenesis through controlling transcriptome fate and function |
title_full | RNA structural dynamics regulate early embryogenesis through controlling transcriptome fate and function |
title_fullStr | RNA structural dynamics regulate early embryogenesis through controlling transcriptome fate and function |
title_full_unstemmed | RNA structural dynamics regulate early embryogenesis through controlling transcriptome fate and function |
title_short | RNA structural dynamics regulate early embryogenesis through controlling transcriptome fate and function |
title_sort | rna structural dynamics regulate early embryogenesis through controlling transcriptome fate and function |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7236375/ https://www.ncbi.nlm.nih.gov/pubmed/32423473 http://dx.doi.org/10.1186/s13059-020-02022-2 |
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