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Structural variation and parallel evolution of apomixis in citrus during domestication and diversification

Apomixis, or asexual seed formation, is prevalent in Citrinae via a mechanism termed nucellar or adventitious embryony. Here, multiple embryos of a maternal genotype form directly from nucellar cells in the ovule and can outcompete the developing zygotic embryo as they utilize the sexually derived e...

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Autores principales: Wang, Nan, Song, Xietian, Ye, Junli, Zhang, Siqi, Cao, Zhen, Zhu, Chenqiao, Hu, Jianbing, Zhou, Yin, Huang, Yue, Cao, Shuo, Liu, Zhongjie, Wu, Xiaomeng, Chai, Lijun, Guo, Wenwu, Xu, Qiang, Gaut, Brandon S, Koltunow, Anna M G, Zhou, Yongfeng, Deng, Xiuxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9671666/
https://www.ncbi.nlm.nih.gov/pubmed/36415319
http://dx.doi.org/10.1093/nsr/nwac114
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author Wang, Nan
Song, Xietian
Ye, Junli
Zhang, Siqi
Cao, Zhen
Zhu, Chenqiao
Hu, Jianbing
Zhou, Yin
Huang, Yue
Cao, Shuo
Liu, Zhongjie
Wu, Xiaomeng
Chai, Lijun
Guo, Wenwu
Xu, Qiang
Gaut, Brandon S
Koltunow, Anna M G
Zhou, Yongfeng
Deng, Xiuxin
author_facet Wang, Nan
Song, Xietian
Ye, Junli
Zhang, Siqi
Cao, Zhen
Zhu, Chenqiao
Hu, Jianbing
Zhou, Yin
Huang, Yue
Cao, Shuo
Liu, Zhongjie
Wu, Xiaomeng
Chai, Lijun
Guo, Wenwu
Xu, Qiang
Gaut, Brandon S
Koltunow, Anna M G
Zhou, Yongfeng
Deng, Xiuxin
author_sort Wang, Nan
collection PubMed
description Apomixis, or asexual seed formation, is prevalent in Citrinae via a mechanism termed nucellar or adventitious embryony. Here, multiple embryos of a maternal genotype form directly from nucellar cells in the ovule and can outcompete the developing zygotic embryo as they utilize the sexually derived endosperm for growth. Whilst nucellar embryony enables the propagation of clonal plants of maternal genetic constitution, it is also a barrier to effective breeding through hybridization. To address the genetics and evolution of apomixis in Citrinae, a chromosome-level genome of the Hongkong kumquat (Fortunella hindsii) was assembled following a genome-wide variation map including structural variants (SVs) based on 234 Citrinae accessions. This map revealed that hybrid citrus cultivars shelter genome-wide deleterious mutations and SVs into heterozygous states free from recessive selection, which may explain the capability of nucellar embryony in most cultivars during Citrinae diversification. Analyses revealed that parallel evolution may explain the repeated origin of apomixis in different genera of Citrinae. Within Fortunella, we found that apomixis of some varieties originated via introgression. In apomictic Fortunella, the locus associated with apomixis contains the FhRWP gene, encoding an RWP-RK domain-containing protein previously shown to be required for nucellar embryogenesis in Citrus. We found the heterozygous SV in the FhRWP and CitRWP promoters from apomictic Citrus and Fortunella, due to either two or three miniature inverted transposon element (MITE) insertions. A transcription factor, FhARID, encoding an AT-rich interaction domain-containing protein binds to the MITEs in the promoter of apomictic varieties, which facilitates induction of nucellar embryogenesis. This study provides evolutionary genomic and molecular insights into apomixis in Citrinae and has potential ramifications for citrus breeding.
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spelling pubmed-96716662022-11-21 Structural variation and parallel evolution of apomixis in citrus during domestication and diversification Wang, Nan Song, Xietian Ye, Junli Zhang, Siqi Cao, Zhen Zhu, Chenqiao Hu, Jianbing Zhou, Yin Huang, Yue Cao, Shuo Liu, Zhongjie Wu, Xiaomeng Chai, Lijun Guo, Wenwu Xu, Qiang Gaut, Brandon S Koltunow, Anna M G Zhou, Yongfeng Deng, Xiuxin Natl Sci Rev Research Article Apomixis, or asexual seed formation, is prevalent in Citrinae via a mechanism termed nucellar or adventitious embryony. Here, multiple embryos of a maternal genotype form directly from nucellar cells in the ovule and can outcompete the developing zygotic embryo as they utilize the sexually derived endosperm for growth. Whilst nucellar embryony enables the propagation of clonal plants of maternal genetic constitution, it is also a barrier to effective breeding through hybridization. To address the genetics and evolution of apomixis in Citrinae, a chromosome-level genome of the Hongkong kumquat (Fortunella hindsii) was assembled following a genome-wide variation map including structural variants (SVs) based on 234 Citrinae accessions. This map revealed that hybrid citrus cultivars shelter genome-wide deleterious mutations and SVs into heterozygous states free from recessive selection, which may explain the capability of nucellar embryony in most cultivars during Citrinae diversification. Analyses revealed that parallel evolution may explain the repeated origin of apomixis in different genera of Citrinae. Within Fortunella, we found that apomixis of some varieties originated via introgression. In apomictic Fortunella, the locus associated with apomixis contains the FhRWP gene, encoding an RWP-RK domain-containing protein previously shown to be required for nucellar embryogenesis in Citrus. We found the heterozygous SV in the FhRWP and CitRWP promoters from apomictic Citrus and Fortunella, due to either two or three miniature inverted transposon element (MITE) insertions. A transcription factor, FhARID, encoding an AT-rich interaction domain-containing protein binds to the MITEs in the promoter of apomictic varieties, which facilitates induction of nucellar embryogenesis. This study provides evolutionary genomic and molecular insights into apomixis in Citrinae and has potential ramifications for citrus breeding. Oxford University Press 2022-06-14 /pmc/articles/PMC9671666/ /pubmed/36415319 http://dx.doi.org/10.1093/nsr/nwac114 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of China Science Publishing & Media Ltd. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wang, Nan
Song, Xietian
Ye, Junli
Zhang, Siqi
Cao, Zhen
Zhu, Chenqiao
Hu, Jianbing
Zhou, Yin
Huang, Yue
Cao, Shuo
Liu, Zhongjie
Wu, Xiaomeng
Chai, Lijun
Guo, Wenwu
Xu, Qiang
Gaut, Brandon S
Koltunow, Anna M G
Zhou, Yongfeng
Deng, Xiuxin
Structural variation and parallel evolution of apomixis in citrus during domestication and diversification
title Structural variation and parallel evolution of apomixis in citrus during domestication and diversification
title_full Structural variation and parallel evolution of apomixis in citrus during domestication and diversification
title_fullStr Structural variation and parallel evolution of apomixis in citrus during domestication and diversification
title_full_unstemmed Structural variation and parallel evolution of apomixis in citrus during domestication and diversification
title_short Structural variation and parallel evolution of apomixis in citrus during domestication and diversification
title_sort structural variation and parallel evolution of apomixis in citrus during domestication and diversification
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9671666/
https://www.ncbi.nlm.nih.gov/pubmed/36415319
http://dx.doi.org/10.1093/nsr/nwac114
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