Cargando…

Symmetric subgenomes and balanced homoeolog expression stabilize the establishment of allopolyploidy in cyprinid fish

BACKGROUND: Interspecific postzygotic reproduction isolation results from large genetic divergence between the subgenomes of established hybrids. Polyploidization immediately after hybridization may reset patterns of homologous chromosome pairing and ameliorate deleterious genomic incompatibility be...

Descripción completa

Detalles Bibliográficos
Autores principales: Ren, Li, Gao, Xin, Cui, Jialin, Zhang, Chun, Dai, He, Luo, Mengxue, He, Shaofang, Qin, Qinbo, Luo, Kaikun, Tao, Min, Xiao, Jun, Wang, Jing, Zhang, Hong, Zhang, Xueyin, Zhou, Yi, Zhao, Xin, Liu, Guiming, Wang, Guoliang, Huo, Linhe, Wang, Shi, Hu, Fangzhou, Zhao, Rurong, Zhou, Rong, Wang, Yude, Liu, Qinfeng, Yan, Xiaojing, Wu, Chang, Yang, Conghui, Tang, Chenchen, Duan, Wei, Liu, Shaojun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9472340/
https://www.ncbi.nlm.nih.gov/pubmed/36100845
http://dx.doi.org/10.1186/s12915-022-01401-4
_version_ 1784789284747739136
author Ren, Li
Gao, Xin
Cui, Jialin
Zhang, Chun
Dai, He
Luo, Mengxue
He, Shaofang
Qin, Qinbo
Luo, Kaikun
Tao, Min
Xiao, Jun
Wang, Jing
Zhang, Hong
Zhang, Xueyin
Zhou, Yi
Wang, Jing
Zhao, Xin
Liu, Guiming
Wang, Guoliang
Huo, Linhe
Wang, Shi
Hu, Fangzhou
Zhao, Rurong
Zhou, Rong
Wang, Yude
Liu, Qinfeng
Yan, Xiaojing
Wu, Chang
Yang, Conghui
Tang, Chenchen
Duan, Wei
Liu, Shaojun
author_facet Ren, Li
Gao, Xin
Cui, Jialin
Zhang, Chun
Dai, He
Luo, Mengxue
He, Shaofang
Qin, Qinbo
Luo, Kaikun
Tao, Min
Xiao, Jun
Wang, Jing
Zhang, Hong
Zhang, Xueyin
Zhou, Yi
Wang, Jing
Zhao, Xin
Liu, Guiming
Wang, Guoliang
Huo, Linhe
Wang, Shi
Hu, Fangzhou
Zhao, Rurong
Zhou, Rong
Wang, Yude
Liu, Qinfeng
Yan, Xiaojing
Wu, Chang
Yang, Conghui
Tang, Chenchen
Duan, Wei
Liu, Shaojun
author_sort Ren, Li
collection PubMed
description BACKGROUND: Interspecific postzygotic reproduction isolation results from large genetic divergence between the subgenomes of established hybrids. Polyploidization immediately after hybridization may reset patterns of homologous chromosome pairing and ameliorate deleterious genomic incompatibility between the subgenomes of distinct parental species in plants and animals. However, the observation that polyploidy is less common in vertebrates raises the question of which factors restrict its emergence. Here, we perform analyses of the genome, epigenome, and gene expression in the nascent allotetraploid lineage (2.95 Gb) derived from the intergeneric hybridization of female goldfish (Carassius auratus, 1.49 Gb) and male common carp (Cyprinus carpio, 1.42 Gb), to shed light on the changes leading to the stabilization of hybrids. RESULTS: We firstly identify the two subgenomes derived from the parental lineages of goldfish and common carp. We find variable unequal homoeologous recombination in somatic and germ cells of the intergeneric F(1) and allotetraploid (F(22) and F(24)) populations, reflecting high plasticity between the subgenomes, and rapidly varying copy numbers between the homoeolog genes. We also find dynamic changes in transposable elements accompanied by genome merger and duplication in the allotetraploid lineage. Finally, we observe the gradual decreases in cis-regulatory effects and increases in trans-regulatory effects along with the allotetraploidization, which contribute to increases in the symmetrical homoeologous expression in different tissues and developmental stages, especially in early embryogenesis. CONCLUSIONS: Our results reveal a series of changes in transposable elements, unequal homoeologous recombination, cis- and trans-regulations (e.g. DNA methylation), and homoeologous expression, suggesting their potential roles in mediating adaptive stabilization of regulatory systems of the nascent allotetraploid lineage. The symmetrical subgenomes and homoeologous expression provide a novel way of balancing genetic incompatibilities, providing a new insight into the early stages of allopolyploidization in vertebrate evolution. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-022-01401-4.
format Online
Article
Text
id pubmed-9472340
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-94723402022-09-15 Symmetric subgenomes and balanced homoeolog expression stabilize the establishment of allopolyploidy in cyprinid fish Ren, Li Gao, Xin Cui, Jialin Zhang, Chun Dai, He Luo, Mengxue He, Shaofang Qin, Qinbo Luo, Kaikun Tao, Min Xiao, Jun Wang, Jing Zhang, Hong Zhang, Xueyin Zhou, Yi Wang, Jing Zhao, Xin Liu, Guiming Wang, Guoliang Huo, Linhe Wang, Shi Hu, Fangzhou Zhao, Rurong Zhou, Rong Wang, Yude Liu, Qinfeng Yan, Xiaojing Wu, Chang Yang, Conghui Tang, Chenchen Duan, Wei Liu, Shaojun BMC Biol Research Article BACKGROUND: Interspecific postzygotic reproduction isolation results from large genetic divergence between the subgenomes of established hybrids. Polyploidization immediately after hybridization may reset patterns of homologous chromosome pairing and ameliorate deleterious genomic incompatibility between the subgenomes of distinct parental species in plants and animals. However, the observation that polyploidy is less common in vertebrates raises the question of which factors restrict its emergence. Here, we perform analyses of the genome, epigenome, and gene expression in the nascent allotetraploid lineage (2.95 Gb) derived from the intergeneric hybridization of female goldfish (Carassius auratus, 1.49 Gb) and male common carp (Cyprinus carpio, 1.42 Gb), to shed light on the changes leading to the stabilization of hybrids. RESULTS: We firstly identify the two subgenomes derived from the parental lineages of goldfish and common carp. We find variable unequal homoeologous recombination in somatic and germ cells of the intergeneric F(1) and allotetraploid (F(22) and F(24)) populations, reflecting high plasticity between the subgenomes, and rapidly varying copy numbers between the homoeolog genes. We also find dynamic changes in transposable elements accompanied by genome merger and duplication in the allotetraploid lineage. Finally, we observe the gradual decreases in cis-regulatory effects and increases in trans-regulatory effects along with the allotetraploidization, which contribute to increases in the symmetrical homoeologous expression in different tissues and developmental stages, especially in early embryogenesis. CONCLUSIONS: Our results reveal a series of changes in transposable elements, unequal homoeologous recombination, cis- and trans-regulations (e.g. DNA methylation), and homoeologous expression, suggesting their potential roles in mediating adaptive stabilization of regulatory systems of the nascent allotetraploid lineage. The symmetrical subgenomes and homoeologous expression provide a novel way of balancing genetic incompatibilities, providing a new insight into the early stages of allopolyploidization in vertebrate evolution. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-022-01401-4. BioMed Central 2022-09-14 /pmc/articles/PMC9472340/ /pubmed/36100845 http://dx.doi.org/10.1186/s12915-022-01401-4 Text en © The Author(s) 2022 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
Ren, Li
Gao, Xin
Cui, Jialin
Zhang, Chun
Dai, He
Luo, Mengxue
He, Shaofang
Qin, Qinbo
Luo, Kaikun
Tao, Min
Xiao, Jun
Wang, Jing
Zhang, Hong
Zhang, Xueyin
Zhou, Yi
Wang, Jing
Zhao, Xin
Liu, Guiming
Wang, Guoliang
Huo, Linhe
Wang, Shi
Hu, Fangzhou
Zhao, Rurong
Zhou, Rong
Wang, Yude
Liu, Qinfeng
Yan, Xiaojing
Wu, Chang
Yang, Conghui
Tang, Chenchen
Duan, Wei
Liu, Shaojun
Symmetric subgenomes and balanced homoeolog expression stabilize the establishment of allopolyploidy in cyprinid fish
title Symmetric subgenomes and balanced homoeolog expression stabilize the establishment of allopolyploidy in cyprinid fish
title_full Symmetric subgenomes and balanced homoeolog expression stabilize the establishment of allopolyploidy in cyprinid fish
title_fullStr Symmetric subgenomes and balanced homoeolog expression stabilize the establishment of allopolyploidy in cyprinid fish
title_full_unstemmed Symmetric subgenomes and balanced homoeolog expression stabilize the establishment of allopolyploidy in cyprinid fish
title_short Symmetric subgenomes and balanced homoeolog expression stabilize the establishment of allopolyploidy in cyprinid fish
title_sort symmetric subgenomes and balanced homoeolog expression stabilize the establishment of allopolyploidy in cyprinid fish
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9472340/
https://www.ncbi.nlm.nih.gov/pubmed/36100845
http://dx.doi.org/10.1186/s12915-022-01401-4
work_keys_str_mv AT renli symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT gaoxin symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT cuijialin symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT zhangchun symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT daihe symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT luomengxue symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT heshaofang symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT qinqinbo symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT luokaikun symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT taomin symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT xiaojun symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT wangjing symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT zhanghong symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT zhangxueyin symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT zhouyi symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT wangjing symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT zhaoxin symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT liuguiming symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT wangguoliang symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT huolinhe symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT wangshi symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT hufangzhou symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT zhaorurong symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT zhourong symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT wangyude symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT liuqinfeng symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT yanxiaojing symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT wuchang symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT yangconghui symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT tangchenchen symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT duanwei symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish
AT liushaojun symmetricsubgenomesandbalancedhomoeologexpressionstabilizetheestablishmentofallopolyploidyincyprinidfish