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Trade-off in genome turnover events leading to adaptive evolution of Microcystis aeruginosa species complex
BACKGROUND: Numerous studies in the past have expanded our understanding of the genetic differences of global distributed cyanobacteria that originated around billions of years ago, however, unraveling how gene gain and loss drive the genetic evolution of cyanobacterial species, and the trade-off of...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10433662/ https://www.ncbi.nlm.nih.gov/pubmed/37592233 http://dx.doi.org/10.1186/s12864-023-09555-3 |
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author | Zhang, Xian Xiao, Lijun Liu, Jiahui Tian, Qibai Xie, Jiaqi |
author_facet | Zhang, Xian Xiao, Lijun Liu, Jiahui Tian, Qibai Xie, Jiaqi |
author_sort | Zhang, Xian |
collection | PubMed |
description | BACKGROUND: Numerous studies in the past have expanded our understanding of the genetic differences of global distributed cyanobacteria that originated around billions of years ago, however, unraveling how gene gain and loss drive the genetic evolution of cyanobacterial species, and the trade-off of these evolutionary forces are still the central but poorly understood issues. RESULTS: To delineate the contribution of gene flow in mediating the hereditary differentiation and shaping the microbial evolution, a global genome-wide study of bloom-forming cyanobacterium, Microcystis aeruginosa species complex, provided robust evidence for genetic diversity, reflected by enormous variation in gene repertoire among various strains. Mathematical extrapolation showed an ‘open’ microbial pan-genome of M. aeruginosa species, since novel genes were predicted to be introduced after new genomes were sequenced. Identification of numerous horizontal gene transfer’s signatures in genome regions of interest suggested that genome expansion via transformation and phage-mediated transduction across bacterial lineage as an evolutionary route may contribute to the differentiation of Microcystis functions (e.g., carbohydrate metabolism, amino acid metabolism, and energy metabolism). Meanwhile, the selective loss of some dispensable genes at the cost of metabolic versatility is as a mean of adaptive evolution that has the potential to increase the biological fitness. CONCLUSIONS: Now that the recruitment of novel genes was accompanied by a parallel loss of some other ones, a trade-off in gene content may drive the divergent differentiation of M. aeruginosa genomes. Our study provides a genetic framework for the evolution of M. aeruginosa species and illustrates their possible evolutionary patterns. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09555-3. |
format | Online Article Text |
id | pubmed-10433662 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-104336622023-08-18 Trade-off in genome turnover events leading to adaptive evolution of Microcystis aeruginosa species complex Zhang, Xian Xiao, Lijun Liu, Jiahui Tian, Qibai Xie, Jiaqi BMC Genomics Research BACKGROUND: Numerous studies in the past have expanded our understanding of the genetic differences of global distributed cyanobacteria that originated around billions of years ago, however, unraveling how gene gain and loss drive the genetic evolution of cyanobacterial species, and the trade-off of these evolutionary forces are still the central but poorly understood issues. RESULTS: To delineate the contribution of gene flow in mediating the hereditary differentiation and shaping the microbial evolution, a global genome-wide study of bloom-forming cyanobacterium, Microcystis aeruginosa species complex, provided robust evidence for genetic diversity, reflected by enormous variation in gene repertoire among various strains. Mathematical extrapolation showed an ‘open’ microbial pan-genome of M. aeruginosa species, since novel genes were predicted to be introduced after new genomes were sequenced. Identification of numerous horizontal gene transfer’s signatures in genome regions of interest suggested that genome expansion via transformation and phage-mediated transduction across bacterial lineage as an evolutionary route may contribute to the differentiation of Microcystis functions (e.g., carbohydrate metabolism, amino acid metabolism, and energy metabolism). Meanwhile, the selective loss of some dispensable genes at the cost of metabolic versatility is as a mean of adaptive evolution that has the potential to increase the biological fitness. CONCLUSIONS: Now that the recruitment of novel genes was accompanied by a parallel loss of some other ones, a trade-off in gene content may drive the divergent differentiation of M. aeruginosa genomes. Our study provides a genetic framework for the evolution of M. aeruginosa species and illustrates their possible evolutionary patterns. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09555-3. BioMed Central 2023-08-17 /pmc/articles/PMC10433662/ /pubmed/37592233 http://dx.doi.org/10.1186/s12864-023-09555-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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 Zhang, Xian Xiao, Lijun Liu, Jiahui Tian, Qibai Xie, Jiaqi Trade-off in genome turnover events leading to adaptive evolution of Microcystis aeruginosa species complex |
title | Trade-off in genome turnover events leading to adaptive evolution of Microcystis aeruginosa species complex |
title_full | Trade-off in genome turnover events leading to adaptive evolution of Microcystis aeruginosa species complex |
title_fullStr | Trade-off in genome turnover events leading to adaptive evolution of Microcystis aeruginosa species complex |
title_full_unstemmed | Trade-off in genome turnover events leading to adaptive evolution of Microcystis aeruginosa species complex |
title_short | Trade-off in genome turnover events leading to adaptive evolution of Microcystis aeruginosa species complex |
title_sort | trade-off in genome turnover events leading to adaptive evolution of microcystis aeruginosa species complex |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10433662/ https://www.ncbi.nlm.nih.gov/pubmed/37592233 http://dx.doi.org/10.1186/s12864-023-09555-3 |
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