Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Xian, Xiao, Lijun, Liu, Jiahui, Tian, Qibai, Xie, Jiaqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
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
_version_ 1785091700403732480
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
work_keys_str_mv AT zhangxian tradeoffingenometurnovereventsleadingtoadaptiveevolutionofmicrocystisaeruginosaspeciescomplex
AT xiaolijun tradeoffingenometurnovereventsleadingtoadaptiveevolutionofmicrocystisaeruginosaspeciescomplex
AT liujiahui tradeoffingenometurnovereventsleadingtoadaptiveevolutionofmicrocystisaeruginosaspeciescomplex
AT tianqibai tradeoffingenometurnovereventsleadingtoadaptiveevolutionofmicrocystisaeruginosaspeciescomplex
AT xiejiaqi tradeoffingenometurnovereventsleadingtoadaptiveevolutionofmicrocystisaeruginosaspeciescomplex