Cargando…
Homoeologous Exchanges, Segmental Allopolyploidy, and Polyploid Genome Evolution
Polyploidy is a major force in plant evolution and speciation. In newly formed allopolyploids, pairing between related chromosomes from different subgenomes (homoeologous chromosomes) during meiosis is common. The initial stages of allopolyploid formation are characterized by a spectrum of saltation...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7485112/ https://www.ncbi.nlm.nih.gov/pubmed/33005183 http://dx.doi.org/10.3389/fgene.2020.01014 |
_version_ | 1783581093516017664 |
---|---|
author | Mason, Annaliese S. Wendel, Jonathan F. |
author_facet | Mason, Annaliese S. Wendel, Jonathan F. |
author_sort | Mason, Annaliese S. |
collection | PubMed |
description | Polyploidy is a major force in plant evolution and speciation. In newly formed allopolyploids, pairing between related chromosomes from different subgenomes (homoeologous chromosomes) during meiosis is common. The initial stages of allopolyploid formation are characterized by a spectrum of saltational genomic and regulatory alterations that are responsible for evolutionary novelty. Here we highlight the possible effects and roles of recombination between homoeologous chromosomes during the early stages of allopolyploid stabilization. Homoeologous exchanges (HEs) have been reported in young allopolyploids from across the angiosperms. Although all lineages undergo karyotype change via chromosome rearrangements over time, the early generations after allopolyploid formation are predicted to show an accelerated rate of genomic change. HEs can also cause changes in allele dosage, genome-wide methylation patterns, and downstream phenotypes, and can hence be responsible for speciation and genome stabilization events. Additionally, we propose that fixation of duplication – deletion events resulting from HEs could lead to the production of genomes which appear to be a mix of autopolyploid and allopolyploid segments, sometimes termed “segmental allopolyploids.” We discuss the implications of these findings for our understanding of the relationship between genome instability in novel polyploids and genome evolution. |
format | Online Article Text |
id | pubmed-7485112 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74851122020-09-30 Homoeologous Exchanges, Segmental Allopolyploidy, and Polyploid Genome Evolution Mason, Annaliese S. Wendel, Jonathan F. Front Genet Genetics Polyploidy is a major force in plant evolution and speciation. In newly formed allopolyploids, pairing between related chromosomes from different subgenomes (homoeologous chromosomes) during meiosis is common. The initial stages of allopolyploid formation are characterized by a spectrum of saltational genomic and regulatory alterations that are responsible for evolutionary novelty. Here we highlight the possible effects and roles of recombination between homoeologous chromosomes during the early stages of allopolyploid stabilization. Homoeologous exchanges (HEs) have been reported in young allopolyploids from across the angiosperms. Although all lineages undergo karyotype change via chromosome rearrangements over time, the early generations after allopolyploid formation are predicted to show an accelerated rate of genomic change. HEs can also cause changes in allele dosage, genome-wide methylation patterns, and downstream phenotypes, and can hence be responsible for speciation and genome stabilization events. Additionally, we propose that fixation of duplication – deletion events resulting from HEs could lead to the production of genomes which appear to be a mix of autopolyploid and allopolyploid segments, sometimes termed “segmental allopolyploids.” We discuss the implications of these findings for our understanding of the relationship between genome instability in novel polyploids and genome evolution. Frontiers Media S.A. 2020-08-28 /pmc/articles/PMC7485112/ /pubmed/33005183 http://dx.doi.org/10.3389/fgene.2020.01014 Text en Copyright © 2020 Mason and Wendel. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Mason, Annaliese S. Wendel, Jonathan F. Homoeologous Exchanges, Segmental Allopolyploidy, and Polyploid Genome Evolution |
title | Homoeologous Exchanges, Segmental Allopolyploidy, and Polyploid Genome Evolution |
title_full | Homoeologous Exchanges, Segmental Allopolyploidy, and Polyploid Genome Evolution |
title_fullStr | Homoeologous Exchanges, Segmental Allopolyploidy, and Polyploid Genome Evolution |
title_full_unstemmed | Homoeologous Exchanges, Segmental Allopolyploidy, and Polyploid Genome Evolution |
title_short | Homoeologous Exchanges, Segmental Allopolyploidy, and Polyploid Genome Evolution |
title_sort | homoeologous exchanges, segmental allopolyploidy, and polyploid genome evolution |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7485112/ https://www.ncbi.nlm.nih.gov/pubmed/33005183 http://dx.doi.org/10.3389/fgene.2020.01014 |
work_keys_str_mv | AT masonannalieses homoeologousexchangessegmentalallopolyploidyandpolyploidgenomeevolution AT wendeljonathanf homoeologousexchangessegmentalallopolyploidyandpolyploidgenomeevolution |