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Mitonuclear mismatch alters nuclear gene expression in naturally introgressed Rhinolophus bats

BACKGROUND: Mitochondrial function involves the interplay between mitochondrial and nuclear genomes. Such mitonuclear interactions can be disrupted by the introgression of mitochondrial DNA between taxa or divergent populations. Previous studies of several model systems (e.g. Drosophila) indicate th...

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Autores principales: Ding, Yuting, Chen, Wenli, Li, Qianqian, Rossiter, Stephen J., Mao, Xiuguang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419968/
https://www.ncbi.nlm.nih.gov/pubmed/34488775
http://dx.doi.org/10.1186/s12983-021-00424-x
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author Ding, Yuting
Chen, Wenli
Li, Qianqian
Rossiter, Stephen J.
Mao, Xiuguang
author_facet Ding, Yuting
Chen, Wenli
Li, Qianqian
Rossiter, Stephen J.
Mao, Xiuguang
author_sort Ding, Yuting
collection PubMed
description BACKGROUND: Mitochondrial function involves the interplay between mitochondrial and nuclear genomes. Such mitonuclear interactions can be disrupted by the introgression of mitochondrial DNA between taxa or divergent populations. Previous studies of several model systems (e.g. Drosophila) indicate that the disruption of mitonuclear interactions, termed mitonuclear mismatch, can alter nuclear gene expression, yet few studies have focused on natural populations. RESULTS: Here we study a naturally introgressed population in the secondary contact zone of two subspecies of the intermediate horseshoe bat (Rhinolophus affinis), in which individuals possess either mitonuclear matched or mismatched genotypes. We generated transcriptome data for six tissue types from five mitonuclear matched and five mismatched individuals. Our results revealed strong tissue-specific effects of mitonuclear mismatch on nuclear gene expression with the largest effect seen in pectoral muscle. Moreover, consistent with the hypothesis that genes associated with the response to oxidative stress may be upregulated in mitonuclear mismatched individuals, we identified several such gene candidates, including DNASE1L3, GPx3 and HSPB6 in muscle, and ISG15 and IFI6 in heart. CONCLUSION: Our study reveals how mitonuclear mismatch arising from introgression in natural populations is likely to have fitness consequences. Underlying the processes that maintain mitonuclear discordance is a step forward to understand the role of mitonuclear interactions in population divergence and speciation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12983-021-00424-x.
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spelling pubmed-84199682021-09-09 Mitonuclear mismatch alters nuclear gene expression in naturally introgressed Rhinolophus bats Ding, Yuting Chen, Wenli Li, Qianqian Rossiter, Stephen J. Mao, Xiuguang Front Zool Research BACKGROUND: Mitochondrial function involves the interplay between mitochondrial and nuclear genomes. Such mitonuclear interactions can be disrupted by the introgression of mitochondrial DNA between taxa or divergent populations. Previous studies of several model systems (e.g. Drosophila) indicate that the disruption of mitonuclear interactions, termed mitonuclear mismatch, can alter nuclear gene expression, yet few studies have focused on natural populations. RESULTS: Here we study a naturally introgressed population in the secondary contact zone of two subspecies of the intermediate horseshoe bat (Rhinolophus affinis), in which individuals possess either mitonuclear matched or mismatched genotypes. We generated transcriptome data for six tissue types from five mitonuclear matched and five mismatched individuals. Our results revealed strong tissue-specific effects of mitonuclear mismatch on nuclear gene expression with the largest effect seen in pectoral muscle. Moreover, consistent with the hypothesis that genes associated with the response to oxidative stress may be upregulated in mitonuclear mismatched individuals, we identified several such gene candidates, including DNASE1L3, GPx3 and HSPB6 in muscle, and ISG15 and IFI6 in heart. CONCLUSION: Our study reveals how mitonuclear mismatch arising from introgression in natural populations is likely to have fitness consequences. Underlying the processes that maintain mitonuclear discordance is a step forward to understand the role of mitonuclear interactions in population divergence and speciation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12983-021-00424-x. BioMed Central 2021-09-06 /pmc/articles/PMC8419968/ /pubmed/34488775 http://dx.doi.org/10.1186/s12983-021-00424-x 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
Ding, Yuting
Chen, Wenli
Li, Qianqian
Rossiter, Stephen J.
Mao, Xiuguang
Mitonuclear mismatch alters nuclear gene expression in naturally introgressed Rhinolophus bats
title Mitonuclear mismatch alters nuclear gene expression in naturally introgressed Rhinolophus bats
title_full Mitonuclear mismatch alters nuclear gene expression in naturally introgressed Rhinolophus bats
title_fullStr Mitonuclear mismatch alters nuclear gene expression in naturally introgressed Rhinolophus bats
title_full_unstemmed Mitonuclear mismatch alters nuclear gene expression in naturally introgressed Rhinolophus bats
title_short Mitonuclear mismatch alters nuclear gene expression in naturally introgressed Rhinolophus bats
title_sort mitonuclear mismatch alters nuclear gene expression in naturally introgressed rhinolophus bats
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419968/
https://www.ncbi.nlm.nih.gov/pubmed/34488775
http://dx.doi.org/10.1186/s12983-021-00424-x
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