Cargando…

A genome assembly for Orinus kokonorica provides insights into the origin, adaptive evolution and further diversification of two closely related grass genera

Ancient whole-genome duplication (WGD) or polyploidization is prevalent in plants and has played a crucial role in plant adaptation. However, the underlying genomic basis of ecological adaptation and subsequent diversification after WGD are still poorly understood in most plants. Here, we report a c...

Descripción completa

Detalles Bibliográficos
Autores principales: Qu, Kunjing, Liu, Ai, Yin, Mou, Mu, Wenjie, Wu, Shuang, Hu, Hongyin, Chen, Jinyuan, Su, Xu, Dou, Quanwen, Ren, Guangpeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10693610/
https://www.ncbi.nlm.nih.gov/pubmed/38042963
http://dx.doi.org/10.1038/s42003-023-05620-5
_version_ 1785153200079241216
author Qu, Kunjing
Liu, Ai
Yin, Mou
Mu, Wenjie
Wu, Shuang
Hu, Hongyin
Chen, Jinyuan
Su, Xu
Dou, Quanwen
Ren, Guangpeng
author_facet Qu, Kunjing
Liu, Ai
Yin, Mou
Mu, Wenjie
Wu, Shuang
Hu, Hongyin
Chen, Jinyuan
Su, Xu
Dou, Quanwen
Ren, Guangpeng
author_sort Qu, Kunjing
collection PubMed
description Ancient whole-genome duplication (WGD) or polyploidization is prevalent in plants and has played a crucial role in plant adaptation. However, the underlying genomic basis of ecological adaptation and subsequent diversification after WGD are still poorly understood in most plants. Here, we report a chromosome-scale genome assembly for the genus Orinus (Orinus kokonorica as representative) and preform comparative genomics with its closely related genus Cleistogenes (Cleistogenes songorica as representative), both belonging to a newly named subtribe Orininae of the grass subfamily Chloridoideae. The two genera may share one paleo-allotetraploidy event before 10 million years ago, and the two subgenomes of O. kokonorica display neither fractionation bias nor global homoeolog expression dominance. We find substantial genome rearrangements and extensive structural variations (SVs) between the two species. With comparative transcriptomics, we demonstrate that functional innovations of orthologous genes may have played an important role in promoting adaptive evolution and diversification of the two genera after polyploidization. In addition, copy number variations and extensive SVs between orthologs of flower and rhizome related genes may contribute to the morphological differences between the two genera. Our results provide new insights into the adaptive evolution and subsequent diversification of the two genera after polyploidization.
format Online
Article
Text
id pubmed-10693610
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-106936102023-12-04 A genome assembly for Orinus kokonorica provides insights into the origin, adaptive evolution and further diversification of two closely related grass genera Qu, Kunjing Liu, Ai Yin, Mou Mu, Wenjie Wu, Shuang Hu, Hongyin Chen, Jinyuan Su, Xu Dou, Quanwen Ren, Guangpeng Commun Biol Article Ancient whole-genome duplication (WGD) or polyploidization is prevalent in plants and has played a crucial role in plant adaptation. However, the underlying genomic basis of ecological adaptation and subsequent diversification after WGD are still poorly understood in most plants. Here, we report a chromosome-scale genome assembly for the genus Orinus (Orinus kokonorica as representative) and preform comparative genomics with its closely related genus Cleistogenes (Cleistogenes songorica as representative), both belonging to a newly named subtribe Orininae of the grass subfamily Chloridoideae. The two genera may share one paleo-allotetraploidy event before 10 million years ago, and the two subgenomes of O. kokonorica display neither fractionation bias nor global homoeolog expression dominance. We find substantial genome rearrangements and extensive structural variations (SVs) between the two species. With comparative transcriptomics, we demonstrate that functional innovations of orthologous genes may have played an important role in promoting adaptive evolution and diversification of the two genera after polyploidization. In addition, copy number variations and extensive SVs between orthologs of flower and rhizome related genes may contribute to the morphological differences between the two genera. Our results provide new insights into the adaptive evolution and subsequent diversification of the two genera after polyploidization. Nature Publishing Group UK 2023-12-02 /pmc/articles/PMC10693610/ /pubmed/38042963 http://dx.doi.org/10.1038/s42003-023-05620-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) .
spellingShingle Article
Qu, Kunjing
Liu, Ai
Yin, Mou
Mu, Wenjie
Wu, Shuang
Hu, Hongyin
Chen, Jinyuan
Su, Xu
Dou, Quanwen
Ren, Guangpeng
A genome assembly for Orinus kokonorica provides insights into the origin, adaptive evolution and further diversification of two closely related grass genera
title A genome assembly for Orinus kokonorica provides insights into the origin, adaptive evolution and further diversification of two closely related grass genera
title_full A genome assembly for Orinus kokonorica provides insights into the origin, adaptive evolution and further diversification of two closely related grass genera
title_fullStr A genome assembly for Orinus kokonorica provides insights into the origin, adaptive evolution and further diversification of two closely related grass genera
title_full_unstemmed A genome assembly for Orinus kokonorica provides insights into the origin, adaptive evolution and further diversification of two closely related grass genera
title_short A genome assembly for Orinus kokonorica provides insights into the origin, adaptive evolution and further diversification of two closely related grass genera
title_sort genome assembly for orinus kokonorica provides insights into the origin, adaptive evolution and further diversification of two closely related grass genera
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10693610/
https://www.ncbi.nlm.nih.gov/pubmed/38042963
http://dx.doi.org/10.1038/s42003-023-05620-5
work_keys_str_mv AT qukunjing agenomeassemblyfororinuskokonoricaprovidesinsightsintotheoriginadaptiveevolutionandfurtherdiversificationoftwocloselyrelatedgrassgenera
AT liuai agenomeassemblyfororinuskokonoricaprovidesinsightsintotheoriginadaptiveevolutionandfurtherdiversificationoftwocloselyrelatedgrassgenera
AT yinmou agenomeassemblyfororinuskokonoricaprovidesinsightsintotheoriginadaptiveevolutionandfurtherdiversificationoftwocloselyrelatedgrassgenera
AT muwenjie agenomeassemblyfororinuskokonoricaprovidesinsightsintotheoriginadaptiveevolutionandfurtherdiversificationoftwocloselyrelatedgrassgenera
AT wushuang agenomeassemblyfororinuskokonoricaprovidesinsightsintotheoriginadaptiveevolutionandfurtherdiversificationoftwocloselyrelatedgrassgenera
AT huhongyin agenomeassemblyfororinuskokonoricaprovidesinsightsintotheoriginadaptiveevolutionandfurtherdiversificationoftwocloselyrelatedgrassgenera
AT chenjinyuan agenomeassemblyfororinuskokonoricaprovidesinsightsintotheoriginadaptiveevolutionandfurtherdiversificationoftwocloselyrelatedgrassgenera
AT suxu agenomeassemblyfororinuskokonoricaprovidesinsightsintotheoriginadaptiveevolutionandfurtherdiversificationoftwocloselyrelatedgrassgenera
AT douquanwen agenomeassemblyfororinuskokonoricaprovidesinsightsintotheoriginadaptiveevolutionandfurtherdiversificationoftwocloselyrelatedgrassgenera
AT renguangpeng agenomeassemblyfororinuskokonoricaprovidesinsightsintotheoriginadaptiveevolutionandfurtherdiversificationoftwocloselyrelatedgrassgenera
AT qukunjing genomeassemblyfororinuskokonoricaprovidesinsightsintotheoriginadaptiveevolutionandfurtherdiversificationoftwocloselyrelatedgrassgenera
AT liuai genomeassemblyfororinuskokonoricaprovidesinsightsintotheoriginadaptiveevolutionandfurtherdiversificationoftwocloselyrelatedgrassgenera
AT yinmou genomeassemblyfororinuskokonoricaprovidesinsightsintotheoriginadaptiveevolutionandfurtherdiversificationoftwocloselyrelatedgrassgenera
AT muwenjie genomeassemblyfororinuskokonoricaprovidesinsightsintotheoriginadaptiveevolutionandfurtherdiversificationoftwocloselyrelatedgrassgenera
AT wushuang genomeassemblyfororinuskokonoricaprovidesinsightsintotheoriginadaptiveevolutionandfurtherdiversificationoftwocloselyrelatedgrassgenera
AT huhongyin genomeassemblyfororinuskokonoricaprovidesinsightsintotheoriginadaptiveevolutionandfurtherdiversificationoftwocloselyrelatedgrassgenera
AT chenjinyuan genomeassemblyfororinuskokonoricaprovidesinsightsintotheoriginadaptiveevolutionandfurtherdiversificationoftwocloselyrelatedgrassgenera
AT suxu genomeassemblyfororinuskokonoricaprovidesinsightsintotheoriginadaptiveevolutionandfurtherdiversificationoftwocloselyrelatedgrassgenera
AT douquanwen genomeassemblyfororinuskokonoricaprovidesinsightsintotheoriginadaptiveevolutionandfurtherdiversificationoftwocloselyrelatedgrassgenera
AT renguangpeng genomeassemblyfororinuskokonoricaprovidesinsightsintotheoriginadaptiveevolutionandfurtherdiversificationoftwocloselyrelatedgrassgenera