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Pan-mitogenomics reveals the genetic basis of cytonuclear conflicts in citrus hybridization, domestication, and diversification

Although interactions between the cytoplasmic and nuclear genomes occurred during diversification of many plants, the evolutionary conflicts due to cytonuclear interactions are poorly understood in crop breeding. Here, we constructed a pan-mitogenome and identified chimeric open reading frames (ORFs...

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Autores principales: Wang, Nan, Li, Chaochao, Kuang, Lihua, Wu, Xiaomeng, Xie, Kaidong, Zhu, Andan, Xu, Qiang, Larkin, Robert M., Zhou, Yongfeng, Deng, Xiuxin, Guo, Wenwu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618123/
https://www.ncbi.nlm.nih.gov/pubmed/36260744
http://dx.doi.org/10.1073/pnas.2206076119
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author Wang, Nan
Li, Chaochao
Kuang, Lihua
Wu, Xiaomeng
Xie, Kaidong
Zhu, Andan
Xu, Qiang
Larkin, Robert M.
Zhou, Yongfeng
Deng, Xiuxin
Guo, Wenwu
author_facet Wang, Nan
Li, Chaochao
Kuang, Lihua
Wu, Xiaomeng
Xie, Kaidong
Zhu, Andan
Xu, Qiang
Larkin, Robert M.
Zhou, Yongfeng
Deng, Xiuxin
Guo, Wenwu
author_sort Wang, Nan
collection PubMed
description Although interactions between the cytoplasmic and nuclear genomes occurred during diversification of many plants, the evolutionary conflicts due to cytonuclear interactions are poorly understood in crop breeding. Here, we constructed a pan-mitogenome and identified chimeric open reading frames (ORFs) generated by extensive structural variations (SVs). Meanwhile, short reads from 184 accessions of citrus species were combined to construct three variation maps for the nuclear, mitochondrial, and chloroplast genomes. The population genomic data showed discordant topologies between the cytoplasmic and nuclear genomes because of differences in mutation rates and levels of heteroplasmy from paternal leakage. An analysis of species-specific SVs indicated that mitochondrial heteroplasmy was common and that chloroplast heteroplasmy was undetectable. Interestingly, we found a prominent divergence in the mitogenomes and the highest genetic load in the, which may provide the basis for cytoplasmic male sterility (CMS) and thus influence the reshuffling of the cytoplasmic and nuclear genomes during hybridization. Using cytoplasmic replacement experiments, we identified a type of species-specific CMS in mandarin related to two chimeric mitochondrial genes. Our analyses indicate that cytoplasmic genomes from mandarin have rarely been maintained in hybrids and that paternal leakage produced very low levels of mitochondrial heteroplasmy in mandarin. A genome-wide association study (GWAS) provided evidence for three nuclear genes that encode pentatricopeptide repeat (PPR) proteins contributing to the cytonuclear interactions in the Citrus genus. Our study demonstrates the occurrence of evolutionary conflicts between cytoplasmic and nuclear genomes in citrus and has important implications for genetics and breeding.
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spelling pubmed-96181232023-04-19 Pan-mitogenomics reveals the genetic basis of cytonuclear conflicts in citrus hybridization, domestication, and diversification Wang, Nan Li, Chaochao Kuang, Lihua Wu, Xiaomeng Xie, Kaidong Zhu, Andan Xu, Qiang Larkin, Robert M. Zhou, Yongfeng Deng, Xiuxin Guo, Wenwu Proc Natl Acad Sci U S A Biological Sciences Although interactions between the cytoplasmic and nuclear genomes occurred during diversification of many plants, the evolutionary conflicts due to cytonuclear interactions are poorly understood in crop breeding. Here, we constructed a pan-mitogenome and identified chimeric open reading frames (ORFs) generated by extensive structural variations (SVs). Meanwhile, short reads from 184 accessions of citrus species were combined to construct three variation maps for the nuclear, mitochondrial, and chloroplast genomes. The population genomic data showed discordant topologies between the cytoplasmic and nuclear genomes because of differences in mutation rates and levels of heteroplasmy from paternal leakage. An analysis of species-specific SVs indicated that mitochondrial heteroplasmy was common and that chloroplast heteroplasmy was undetectable. Interestingly, we found a prominent divergence in the mitogenomes and the highest genetic load in the, which may provide the basis for cytoplasmic male sterility (CMS) and thus influence the reshuffling of the cytoplasmic and nuclear genomes during hybridization. Using cytoplasmic replacement experiments, we identified a type of species-specific CMS in mandarin related to two chimeric mitochondrial genes. Our analyses indicate that cytoplasmic genomes from mandarin have rarely been maintained in hybrids and that paternal leakage produced very low levels of mitochondrial heteroplasmy in mandarin. A genome-wide association study (GWAS) provided evidence for three nuclear genes that encode pentatricopeptide repeat (PPR) proteins contributing to the cytonuclear interactions in the Citrus genus. Our study demonstrates the occurrence of evolutionary conflicts between cytoplasmic and nuclear genomes in citrus and has important implications for genetics and breeding. National Academy of Sciences 2022-10-19 2022-10-25 /pmc/articles/PMC9618123/ /pubmed/36260744 http://dx.doi.org/10.1073/pnas.2206076119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Wang, Nan
Li, Chaochao
Kuang, Lihua
Wu, Xiaomeng
Xie, Kaidong
Zhu, Andan
Xu, Qiang
Larkin, Robert M.
Zhou, Yongfeng
Deng, Xiuxin
Guo, Wenwu
Pan-mitogenomics reveals the genetic basis of cytonuclear conflicts in citrus hybridization, domestication, and diversification
title Pan-mitogenomics reveals the genetic basis of cytonuclear conflicts in citrus hybridization, domestication, and diversification
title_full Pan-mitogenomics reveals the genetic basis of cytonuclear conflicts in citrus hybridization, domestication, and diversification
title_fullStr Pan-mitogenomics reveals the genetic basis of cytonuclear conflicts in citrus hybridization, domestication, and diversification
title_full_unstemmed Pan-mitogenomics reveals the genetic basis of cytonuclear conflicts in citrus hybridization, domestication, and diversification
title_short Pan-mitogenomics reveals the genetic basis of cytonuclear conflicts in citrus hybridization, domestication, and diversification
title_sort pan-mitogenomics reveals the genetic basis of cytonuclear conflicts in citrus hybridization, domestication, and diversification
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618123/
https://www.ncbi.nlm.nih.gov/pubmed/36260744
http://dx.doi.org/10.1073/pnas.2206076119
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