Cargando…

Gene duplication and evolution in recurring polyploidization–diploidization cycles in plants

BACKGROUND: The sharp increase of plant genome and transcriptome data provide valuable resources to investigate evolutionary consequences of gene duplication in a range of taxa, and unravel common principles underlying duplicate gene retention. RESULTS: We survey 141 sequenced plant genomes to eluci...

Descripción completa

Detalles Bibliográficos
Autores principales: Qiao, Xin, Li, Qionghou, Yin, Hao, Qi, Kaijie, Li, Leiting, Wang, Runze, Zhang, Shaoling, Paterson, Andrew H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6383267/
https://www.ncbi.nlm.nih.gov/pubmed/30791939
http://dx.doi.org/10.1186/s13059-019-1650-2
_version_ 1783396810763534336
author Qiao, Xin
Li, Qionghou
Yin, Hao
Qi, Kaijie
Li, Leiting
Wang, Runze
Zhang, Shaoling
Paterson, Andrew H.
author_facet Qiao, Xin
Li, Qionghou
Yin, Hao
Qi, Kaijie
Li, Leiting
Wang, Runze
Zhang, Shaoling
Paterson, Andrew H.
author_sort Qiao, Xin
collection PubMed
description BACKGROUND: The sharp increase of plant genome and transcriptome data provide valuable resources to investigate evolutionary consequences of gene duplication in a range of taxa, and unravel common principles underlying duplicate gene retention. RESULTS: We survey 141 sequenced plant genomes to elucidate consequences of gene and genome duplication, processes central to the evolution of biodiversity. We develop a pipeline named DupGen_finder to identify different modes of gene duplication in plants. Genes derived from whole-genome, tandem, proximal, transposed, or dispersed duplication differ in abundance, selection pressure, expression divergence, and gene conversion rate among genomes. The number of WGD-derived duplicate genes decreases exponentially with increasing age of duplication events—transposed duplication- and dispersed duplication-derived genes declined in parallel. In contrast, the frequency of tandem and proximal duplications showed no significant decrease over time, providing a continuous supply of variants available for adaptation to continuously changing environments. Moreover, tandem and proximal duplicates experienced stronger selective pressure than genes formed by other modes and evolved toward biased functional roles involved in plant self-defense. The rate of gene conversion among WGD-derived gene pairs declined over time, peaking shortly after polyploidization. To provide a platform for accessing duplicated gene pairs in different plants, we constructed the Plant Duplicate Gene Database. CONCLUSIONS: We identify a comprehensive landscape of different modes of gene duplication across the plant kingdom by comparing 141 genomes, which provides a solid foundation for further investigation of the dynamic evolution of duplicate genes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13059-019-1650-2) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6383267
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-63832672019-03-01 Gene duplication and evolution in recurring polyploidization–diploidization cycles in plants Qiao, Xin Li, Qionghou Yin, Hao Qi, Kaijie Li, Leiting Wang, Runze Zhang, Shaoling Paterson, Andrew H. Genome Biol Research BACKGROUND: The sharp increase of plant genome and transcriptome data provide valuable resources to investigate evolutionary consequences of gene duplication in a range of taxa, and unravel common principles underlying duplicate gene retention. RESULTS: We survey 141 sequenced plant genomes to elucidate consequences of gene and genome duplication, processes central to the evolution of biodiversity. We develop a pipeline named DupGen_finder to identify different modes of gene duplication in plants. Genes derived from whole-genome, tandem, proximal, transposed, or dispersed duplication differ in abundance, selection pressure, expression divergence, and gene conversion rate among genomes. The number of WGD-derived duplicate genes decreases exponentially with increasing age of duplication events—transposed duplication- and dispersed duplication-derived genes declined in parallel. In contrast, the frequency of tandem and proximal duplications showed no significant decrease over time, providing a continuous supply of variants available for adaptation to continuously changing environments. Moreover, tandem and proximal duplicates experienced stronger selective pressure than genes formed by other modes and evolved toward biased functional roles involved in plant self-defense. The rate of gene conversion among WGD-derived gene pairs declined over time, peaking shortly after polyploidization. To provide a platform for accessing duplicated gene pairs in different plants, we constructed the Plant Duplicate Gene Database. CONCLUSIONS: We identify a comprehensive landscape of different modes of gene duplication across the plant kingdom by comparing 141 genomes, which provides a solid foundation for further investigation of the dynamic evolution of duplicate genes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13059-019-1650-2) contains supplementary material, which is available to authorized users. BioMed Central 2019-02-21 /pmc/articles/PMC6383267/ /pubmed/30791939 http://dx.doi.org/10.1186/s13059-019-1650-2 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Qiao, Xin
Li, Qionghou
Yin, Hao
Qi, Kaijie
Li, Leiting
Wang, Runze
Zhang, Shaoling
Paterson, Andrew H.
Gene duplication and evolution in recurring polyploidization–diploidization cycles in plants
title Gene duplication and evolution in recurring polyploidization–diploidization cycles in plants
title_full Gene duplication and evolution in recurring polyploidization–diploidization cycles in plants
title_fullStr Gene duplication and evolution in recurring polyploidization–diploidization cycles in plants
title_full_unstemmed Gene duplication and evolution in recurring polyploidization–diploidization cycles in plants
title_short Gene duplication and evolution in recurring polyploidization–diploidization cycles in plants
title_sort gene duplication and evolution in recurring polyploidization–diploidization cycles in plants
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6383267/
https://www.ncbi.nlm.nih.gov/pubmed/30791939
http://dx.doi.org/10.1186/s13059-019-1650-2
work_keys_str_mv AT qiaoxin geneduplicationandevolutioninrecurringpolyploidizationdiploidizationcyclesinplants
AT liqionghou geneduplicationandevolutioninrecurringpolyploidizationdiploidizationcyclesinplants
AT yinhao geneduplicationandevolutioninrecurringpolyploidizationdiploidizationcyclesinplants
AT qikaijie geneduplicationandevolutioninrecurringpolyploidizationdiploidizationcyclesinplants
AT lileiting geneduplicationandevolutioninrecurringpolyploidizationdiploidizationcyclesinplants
AT wangrunze geneduplicationandevolutioninrecurringpolyploidizationdiploidizationcyclesinplants
AT zhangshaoling geneduplicationandevolutioninrecurringpolyploidizationdiploidizationcyclesinplants
AT patersonandrewh geneduplicationandevolutioninrecurringpolyploidizationdiploidizationcyclesinplants