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Microhomologies Are Associated with Tandem Duplications and Structural Variation in Plant Mitochondrial Genomes

Short tandem repeats (STRs) contribute to structural variation in plant mitochondrial genomes, but the mechanisms underlying their formation and expansion are unclear. In this study, we detected high polymorphism in the nad7-1 region of the Pinus tabuliformis mitogenome caused by the rapid accumulat...

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Autores principales: Xia, Hanhan, Zhao, Wei, Shi, Yong, Wang, Xiao-Ru, Wang, Baosheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7643612/
https://www.ncbi.nlm.nih.gov/pubmed/32790831
http://dx.doi.org/10.1093/gbe/evaa172
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author Xia, Hanhan
Zhao, Wei
Shi, Yong
Wang, Xiao-Ru
Wang, Baosheng
author_facet Xia, Hanhan
Zhao, Wei
Shi, Yong
Wang, Xiao-Ru
Wang, Baosheng
author_sort Xia, Hanhan
collection PubMed
description Short tandem repeats (STRs) contribute to structural variation in plant mitochondrial genomes, but the mechanisms underlying their formation and expansion are unclear. In this study, we detected high polymorphism in the nad7-1 region of the Pinus tabuliformis mitogenome caused by the rapid accumulation of STRs and rearrangements over a few million years ago. The STRs in nad7-1 have a 7-bp microhomology (TAG7) flanking the repeat array. We then scanned the mitogenomes of 136 seed plants to understand the role of microhomology in the formation of STR and mitogenome evolution. A total of 13,170 STRs were identified, and almost half of them were associated with microhomologies. A substantial amount (1,197) of microhomologies was long enough to mediate structural variation, and the length of microhomology is positively correlated with the length of tandem repeat unit. These results suggest that microhomology may be involved in the formation of tandem repeat via microhomology-mediated pathway, and the formation of longer duplicates required greater length of microhomology. We examined the abundance of these 1,197 microhomologies, and found 75% of them were enriched in the plant mitogenomes. Further analyses of the 400 prevalent microhomologies revealed that 175 of them showed differential enrichment between angiosperms and gymnosperms and 186 differed between angiosperms and conifers, indicating lineage-specific usage and expansion of microhomologies. Our study sheds light on the sources of structural variation in plant mitochondrial genomes and highlights the importance of microhomology in mitochondrial genome evolution.
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spelling pubmed-76436122020-11-12 Microhomologies Are Associated with Tandem Duplications and Structural Variation in Plant Mitochondrial Genomes Xia, Hanhan Zhao, Wei Shi, Yong Wang, Xiao-Ru Wang, Baosheng Genome Biol Evol Research Article Short tandem repeats (STRs) contribute to structural variation in plant mitochondrial genomes, but the mechanisms underlying their formation and expansion are unclear. In this study, we detected high polymorphism in the nad7-1 region of the Pinus tabuliformis mitogenome caused by the rapid accumulation of STRs and rearrangements over a few million years ago. The STRs in nad7-1 have a 7-bp microhomology (TAG7) flanking the repeat array. We then scanned the mitogenomes of 136 seed plants to understand the role of microhomology in the formation of STR and mitogenome evolution. A total of 13,170 STRs were identified, and almost half of them were associated with microhomologies. A substantial amount (1,197) of microhomologies was long enough to mediate structural variation, and the length of microhomology is positively correlated with the length of tandem repeat unit. These results suggest that microhomology may be involved in the formation of tandem repeat via microhomology-mediated pathway, and the formation of longer duplicates required greater length of microhomology. We examined the abundance of these 1,197 microhomologies, and found 75% of them were enriched in the plant mitogenomes. Further analyses of the 400 prevalent microhomologies revealed that 175 of them showed differential enrichment between angiosperms and gymnosperms and 186 differed between angiosperms and conifers, indicating lineage-specific usage and expansion of microhomologies. Our study sheds light on the sources of structural variation in plant mitochondrial genomes and highlights the importance of microhomology in mitochondrial genome evolution. Oxford University Press 2020-08-13 /pmc/articles/PMC7643612/ /pubmed/32790831 http://dx.doi.org/10.1093/gbe/evaa172 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Xia, Hanhan
Zhao, Wei
Shi, Yong
Wang, Xiao-Ru
Wang, Baosheng
Microhomologies Are Associated with Tandem Duplications and Structural Variation in Plant Mitochondrial Genomes
title Microhomologies Are Associated with Tandem Duplications and Structural Variation in Plant Mitochondrial Genomes
title_full Microhomologies Are Associated with Tandem Duplications and Structural Variation in Plant Mitochondrial Genomes
title_fullStr Microhomologies Are Associated with Tandem Duplications and Structural Variation in Plant Mitochondrial Genomes
title_full_unstemmed Microhomologies Are Associated with Tandem Duplications and Structural Variation in Plant Mitochondrial Genomes
title_short Microhomologies Are Associated with Tandem Duplications and Structural Variation in Plant Mitochondrial Genomes
title_sort microhomologies are associated with tandem duplications and structural variation in plant mitochondrial genomes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7643612/
https://www.ncbi.nlm.nih.gov/pubmed/32790831
http://dx.doi.org/10.1093/gbe/evaa172
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