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Wheat in vivo RNA structure landscape reveals a prevalent role of RNA structure in modulating translational subgenome expression asymmetry

BACKGROUND: Polyploidy, especially allopolyploidy, which entails merging divergent genomes via hybridization and whole-genome duplication (WGD), is a major route to speciation in plants. The duplication among the parental genomes (subgenomes) often leads to one subgenome becoming dominant over the o...

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Autores principales: Yang, Xiaofei, Yu, Haopeng, Sun, Wenqing, Ding, Ling, Li, Ji, Cheema, Jitender, Ramirez-Gonzalez, Ricardo, Zhao, Xuebo, Martín, Azahara C., Lu, Fei, Liu, Bao, Uauy, Cristobal, Ding, Yiliang, Zhang, Huakun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8638558/
https://www.ncbi.nlm.nih.gov/pubmed/34847934
http://dx.doi.org/10.1186/s13059-021-02549-y
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author Yang, Xiaofei
Yu, Haopeng
Sun, Wenqing
Ding, Ling
Li, Ji
Cheema, Jitender
Ramirez-Gonzalez, Ricardo
Zhao, Xuebo
Martín, Azahara C.
Lu, Fei
Liu, Bao
Uauy, Cristobal
Ding, Yiliang
Zhang, Huakun
author_facet Yang, Xiaofei
Yu, Haopeng
Sun, Wenqing
Ding, Ling
Li, Ji
Cheema, Jitender
Ramirez-Gonzalez, Ricardo
Zhao, Xuebo
Martín, Azahara C.
Lu, Fei
Liu, Bao
Uauy, Cristobal
Ding, Yiliang
Zhang, Huakun
author_sort Yang, Xiaofei
collection PubMed
description BACKGROUND: Polyploidy, especially allopolyploidy, which entails merging divergent genomes via hybridization and whole-genome duplication (WGD), is a major route to speciation in plants. The duplication among the parental genomes (subgenomes) often leads to one subgenome becoming dominant over the other(s), resulting in subgenome asymmetry in gene content and expression. Polyploid wheats are allopolyploids with most genes present in two (tetraploid) or three (hexaploid) functional copies, which commonly show subgenome expression asymmetry. It is unknown whether a similar subgenome asymmetry exists during translation. We aim to address this key biological question and explore the major contributing factors to subgenome translation asymmetry. RESULTS: Here, we obtain the first tetraploid wheat translatome and reveal that subgenome expression asymmetry exists at the translational level. We further perform in vivo RNA structure profiling to obtain the wheat RNA structure landscape and find that mRNA structure has a strong impact on translation, independent of GC content. We discover a previously uncharacterized contribution of RNA structure in subgenome translation asymmetry. We identify 3564 single-nucleotide variations (SNVs) across the transcriptomes between the two tetraploid wheat subgenomes, which induce large RNA structure disparities. These SNVs are highly conserved within durum wheat cultivars but are divergent in both domesticated and wild emmer wheat. CONCLUSIONS: We successfully determine both the translatome and in vivo RNA structurome in tetraploid wheat. We reveal that RNA structure serves as an important modulator of translational subgenome expression asymmetry in polyploids. Our work provides a new perspective for molecular breeding of major polyploid crops. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-021-02549-y.
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spelling pubmed-86385582021-12-03 Wheat in vivo RNA structure landscape reveals a prevalent role of RNA structure in modulating translational subgenome expression asymmetry Yang, Xiaofei Yu, Haopeng Sun, Wenqing Ding, Ling Li, Ji Cheema, Jitender Ramirez-Gonzalez, Ricardo Zhao, Xuebo Martín, Azahara C. Lu, Fei Liu, Bao Uauy, Cristobal Ding, Yiliang Zhang, Huakun Genome Biol Research BACKGROUND: Polyploidy, especially allopolyploidy, which entails merging divergent genomes via hybridization and whole-genome duplication (WGD), is a major route to speciation in plants. The duplication among the parental genomes (subgenomes) often leads to one subgenome becoming dominant over the other(s), resulting in subgenome asymmetry in gene content and expression. Polyploid wheats are allopolyploids with most genes present in two (tetraploid) or three (hexaploid) functional copies, which commonly show subgenome expression asymmetry. It is unknown whether a similar subgenome asymmetry exists during translation. We aim to address this key biological question and explore the major contributing factors to subgenome translation asymmetry. RESULTS: Here, we obtain the first tetraploid wheat translatome and reveal that subgenome expression asymmetry exists at the translational level. We further perform in vivo RNA structure profiling to obtain the wheat RNA structure landscape and find that mRNA structure has a strong impact on translation, independent of GC content. We discover a previously uncharacterized contribution of RNA structure in subgenome translation asymmetry. We identify 3564 single-nucleotide variations (SNVs) across the transcriptomes between the two tetraploid wheat subgenomes, which induce large RNA structure disparities. These SNVs are highly conserved within durum wheat cultivars but are divergent in both domesticated and wild emmer wheat. CONCLUSIONS: We successfully determine both the translatome and in vivo RNA structurome in tetraploid wheat. We reveal that RNA structure serves as an important modulator of translational subgenome expression asymmetry in polyploids. Our work provides a new perspective for molecular breeding of major polyploid crops. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-021-02549-y. BioMed Central 2021-11-30 /pmc/articles/PMC8638558/ /pubmed/34847934 http://dx.doi.org/10.1186/s13059-021-02549-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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
Yang, Xiaofei
Yu, Haopeng
Sun, Wenqing
Ding, Ling
Li, Ji
Cheema, Jitender
Ramirez-Gonzalez, Ricardo
Zhao, Xuebo
Martín, Azahara C.
Lu, Fei
Liu, Bao
Uauy, Cristobal
Ding, Yiliang
Zhang, Huakun
Wheat in vivo RNA structure landscape reveals a prevalent role of RNA structure in modulating translational subgenome expression asymmetry
title Wheat in vivo RNA structure landscape reveals a prevalent role of RNA structure in modulating translational subgenome expression asymmetry
title_full Wheat in vivo RNA structure landscape reveals a prevalent role of RNA structure in modulating translational subgenome expression asymmetry
title_fullStr Wheat in vivo RNA structure landscape reveals a prevalent role of RNA structure in modulating translational subgenome expression asymmetry
title_full_unstemmed Wheat in vivo RNA structure landscape reveals a prevalent role of RNA structure in modulating translational subgenome expression asymmetry
title_short Wheat in vivo RNA structure landscape reveals a prevalent role of RNA structure in modulating translational subgenome expression asymmetry
title_sort wheat in vivo rna structure landscape reveals a prevalent role of rna structure in modulating translational subgenome expression asymmetry
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8638558/
https://www.ncbi.nlm.nih.gov/pubmed/34847934
http://dx.doi.org/10.1186/s13059-021-02549-y
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