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Cotton D genome assemblies built with long-read data unveil mechanisms of centromere evolution and stress tolerance divergence

BACKGROUND: Many of genome features which could help unravel the often complex post-speciation evolution of closely related species are obscured because of their location in chromosomal regions difficult to accurately characterize using standard genome analysis methods, including centromeres and rep...

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Autores principales: Yang, Zhaoen, Ge, Xiaoyang, Li, Weinan, Jin, Yuying, Liu, Lisen, Hu, Wei, Liu, Fuyan, Chen, Yanli, Peng, Shaoliang, Li, Fuguang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8176745/
https://www.ncbi.nlm.nih.gov/pubmed/34082735
http://dx.doi.org/10.1186/s12915-021-01041-0
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author Yang, Zhaoen
Ge, Xiaoyang
Li, Weinan
Jin, Yuying
Liu, Lisen
Hu, Wei
Liu, Fuyan
Chen, Yanli
Peng, Shaoliang
Li, Fuguang
author_facet Yang, Zhaoen
Ge, Xiaoyang
Li, Weinan
Jin, Yuying
Liu, Lisen
Hu, Wei
Liu, Fuyan
Chen, Yanli
Peng, Shaoliang
Li, Fuguang
author_sort Yang, Zhaoen
collection PubMed
description BACKGROUND: Many of genome features which could help unravel the often complex post-speciation evolution of closely related species are obscured because of their location in chromosomal regions difficult to accurately characterize using standard genome analysis methods, including centromeres and repeat regions. RESULTS: Here, we analyze the genome evolution and diversification of two recently diverged sister cotton species based on nanopore long-read sequence assemblies and Hi-C 3D genome data. Although D genomes are conserved in gene content, they have diversified in gene order, gene structure, gene family diversification, 3D chromatin structure, long-range regulation, and stress-related traits. Inversions predominate among D genome rearrangements. Our results support roles for 5mC and 6mA in gene activation, and 3D chromatin analysis showed that diversification in proximal-vs-distal regulatory-region interactions shape the regulation of defense-related-gene expression. Using a newly developed method, we accurately positioned cotton centromeres and found that these regions have undergone obviously more rapid evolution relative to chromosome arms. We also discovered a cotton-specific LTR class that clarifies evolutionary trajectories among diverse cotton species and identified genetic networks underlying the Verticillium tolerance of Gossypium thurberi (e.g., SA signaling) and salt-stress tolerance of Gossypium davidsonii (e.g., ethylene biosynthesis). Finally, overexpression of G. thurberi genes in upland cotton demonstrated how wild cottons can be exploited for crop improvement. CONCLUSIONS: Our study substantially deepens understanding about how centromeres have developed and evolutionarily impacted the divergence among closely related cotton species and reveals genes and 3D genome structures which can guide basic investigations and applied efforts to improve crops. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-021-01041-0.
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spelling pubmed-81767452021-06-04 Cotton D genome assemblies built with long-read data unveil mechanisms of centromere evolution and stress tolerance divergence Yang, Zhaoen Ge, Xiaoyang Li, Weinan Jin, Yuying Liu, Lisen Hu, Wei Liu, Fuyan Chen, Yanli Peng, Shaoliang Li, Fuguang BMC Biol Research Article BACKGROUND: Many of genome features which could help unravel the often complex post-speciation evolution of closely related species are obscured because of their location in chromosomal regions difficult to accurately characterize using standard genome analysis methods, including centromeres and repeat regions. RESULTS: Here, we analyze the genome evolution and diversification of two recently diverged sister cotton species based on nanopore long-read sequence assemblies and Hi-C 3D genome data. Although D genomes are conserved in gene content, they have diversified in gene order, gene structure, gene family diversification, 3D chromatin structure, long-range regulation, and stress-related traits. Inversions predominate among D genome rearrangements. Our results support roles for 5mC and 6mA in gene activation, and 3D chromatin analysis showed that diversification in proximal-vs-distal regulatory-region interactions shape the regulation of defense-related-gene expression. Using a newly developed method, we accurately positioned cotton centromeres and found that these regions have undergone obviously more rapid evolution relative to chromosome arms. We also discovered a cotton-specific LTR class that clarifies evolutionary trajectories among diverse cotton species and identified genetic networks underlying the Verticillium tolerance of Gossypium thurberi (e.g., SA signaling) and salt-stress tolerance of Gossypium davidsonii (e.g., ethylene biosynthesis). Finally, overexpression of G. thurberi genes in upland cotton demonstrated how wild cottons can be exploited for crop improvement. CONCLUSIONS: Our study substantially deepens understanding about how centromeres have developed and evolutionarily impacted the divergence among closely related cotton species and reveals genes and 3D genome structures which can guide basic investigations and applied efforts to improve crops. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-021-01041-0. BioMed Central 2021-06-03 /pmc/articles/PMC8176745/ /pubmed/34082735 http://dx.doi.org/10.1186/s12915-021-01041-0 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 Article
Yang, Zhaoen
Ge, Xiaoyang
Li, Weinan
Jin, Yuying
Liu, Lisen
Hu, Wei
Liu, Fuyan
Chen, Yanli
Peng, Shaoliang
Li, Fuguang
Cotton D genome assemblies built with long-read data unveil mechanisms of centromere evolution and stress tolerance divergence
title Cotton D genome assemblies built with long-read data unveil mechanisms of centromere evolution and stress tolerance divergence
title_full Cotton D genome assemblies built with long-read data unveil mechanisms of centromere evolution and stress tolerance divergence
title_fullStr Cotton D genome assemblies built with long-read data unveil mechanisms of centromere evolution and stress tolerance divergence
title_full_unstemmed Cotton D genome assemblies built with long-read data unveil mechanisms of centromere evolution and stress tolerance divergence
title_short Cotton D genome assemblies built with long-read data unveil mechanisms of centromere evolution and stress tolerance divergence
title_sort cotton d genome assemblies built with long-read data unveil mechanisms of centromere evolution and stress tolerance divergence
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8176745/
https://www.ncbi.nlm.nih.gov/pubmed/34082735
http://dx.doi.org/10.1186/s12915-021-01041-0
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