Cargando…
Chromosome inheritance and meiotic stability in allopolyploid Brassica napus
Homoeologous recombination, aneuploidy, and other genetic changes are common in resynthesized allopolyploid Brassica napus. In contrast, the chromosomes of cultivars have long been considered to be meiotically stable. To gain a better understanding of the underlying mechanisms leading to stabilizati...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8022990/ https://www.ncbi.nlm.nih.gov/pubmed/33704431 http://dx.doi.org/10.1093/g3journal/jkaa011 |
_version_ | 1783675040681689088 |
---|---|
author | Xiong, Zhiyong Gaeta, Robert T Edger, Patrick P Cao, Yao Zhao, Kanglu Zhang, Siqi Pires, J Chris |
author_facet | Xiong, Zhiyong Gaeta, Robert T Edger, Patrick P Cao, Yao Zhao, Kanglu Zhang, Siqi Pires, J Chris |
author_sort | Xiong, Zhiyong |
collection | PubMed |
description | Homoeologous recombination, aneuploidy, and other genetic changes are common in resynthesized allopolyploid Brassica napus. In contrast, the chromosomes of cultivars have long been considered to be meiotically stable. To gain a better understanding of the underlying mechanisms leading to stabilization in the allopolyploid, the behavior of chromosomes during meiosis can be compared by unambiguous chromosome identification between resynthesized and natural B. napus. Compared with natural B. napus, resynthesized lines show high rates of nonhomologous centromere association, homoeologous recombination leading to translocation, homoeologous chromosome replacement, and association and breakage of 45S rDNA loci. In both natural and resynthesized B. napus, we observed low rates of univalents, A–C bivalents, and early sister chromatid separations. Reciprocal homoeologous chromosome exchanges and double reductions were photographed for the first time in meiotic telophase I. Meiotic errors were non-uniformly distributed across the genome in resynthesized B. napus, and in particular homoeologs sharing synteny along their entire length exhibited multivalents at diakinesis and polysomic inheritance at telophase I. Natural B. napus appeared to resolve meiotic errors mainly by suppressing homoeologous pairing, resolving nonhomologous centromere associations and 45S rDNA associations before diakinesis, and reducing homoeologous cross-overs. |
format | Online Article Text |
id | pubmed-8022990 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-80229902021-04-09 Chromosome inheritance and meiotic stability in allopolyploid Brassica napus Xiong, Zhiyong Gaeta, Robert T Edger, Patrick P Cao, Yao Zhao, Kanglu Zhang, Siqi Pires, J Chris G3 (Bethesda) Investigation Homoeologous recombination, aneuploidy, and other genetic changes are common in resynthesized allopolyploid Brassica napus. In contrast, the chromosomes of cultivars have long been considered to be meiotically stable. To gain a better understanding of the underlying mechanisms leading to stabilization in the allopolyploid, the behavior of chromosomes during meiosis can be compared by unambiguous chromosome identification between resynthesized and natural B. napus. Compared with natural B. napus, resynthesized lines show high rates of nonhomologous centromere association, homoeologous recombination leading to translocation, homoeologous chromosome replacement, and association and breakage of 45S rDNA loci. In both natural and resynthesized B. napus, we observed low rates of univalents, A–C bivalents, and early sister chromatid separations. Reciprocal homoeologous chromosome exchanges and double reductions were photographed for the first time in meiotic telophase I. Meiotic errors were non-uniformly distributed across the genome in resynthesized B. napus, and in particular homoeologs sharing synteny along their entire length exhibited multivalents at diakinesis and polysomic inheritance at telophase I. Natural B. napus appeared to resolve meiotic errors mainly by suppressing homoeologous pairing, resolving nonhomologous centromere associations and 45S rDNA associations before diakinesis, and reducing homoeologous cross-overs. Oxford University Press 2020-12-22 /pmc/articles/PMC8022990/ /pubmed/33704431 http://dx.doi.org/10.1093/g3journal/jkaa011 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Genetics Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Investigation Xiong, Zhiyong Gaeta, Robert T Edger, Patrick P Cao, Yao Zhao, Kanglu Zhang, Siqi Pires, J Chris Chromosome inheritance and meiotic stability in allopolyploid Brassica napus |
title | Chromosome inheritance and meiotic stability in allopolyploid Brassica napus |
title_full | Chromosome inheritance and meiotic stability in allopolyploid Brassica napus |
title_fullStr | Chromosome inheritance and meiotic stability in allopolyploid Brassica napus |
title_full_unstemmed | Chromosome inheritance and meiotic stability in allopolyploid Brassica napus |
title_short | Chromosome inheritance and meiotic stability in allopolyploid Brassica napus |
title_sort | chromosome inheritance and meiotic stability in allopolyploid brassica napus |
topic | Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8022990/ https://www.ncbi.nlm.nih.gov/pubmed/33704431 http://dx.doi.org/10.1093/g3journal/jkaa011 |
work_keys_str_mv | AT xiongzhiyong chromosomeinheritanceandmeioticstabilityinallopolyploidbrassicanapus AT gaetarobertt chromosomeinheritanceandmeioticstabilityinallopolyploidbrassicanapus AT edgerpatrickp chromosomeinheritanceandmeioticstabilityinallopolyploidbrassicanapus AT caoyao chromosomeinheritanceandmeioticstabilityinallopolyploidbrassicanapus AT zhaokanglu chromosomeinheritanceandmeioticstabilityinallopolyploidbrassicanapus AT zhangsiqi chromosomeinheritanceandmeioticstabilityinallopolyploidbrassicanapus AT piresjchris chromosomeinheritanceandmeioticstabilityinallopolyploidbrassicanapus |