Chromosome inheritance and meiotic stability in allopolyploidBrassica napus

Author:

Xiong Zhiyong12ORCID,Gaeta Robert T3,Edger Patrick P24,Cao Yao1,Zhao Kanglu1,Zhang Siqi1,Pires J Chris2ORCID

Affiliation:

1. Key Laboratory of Herbage and Endemic Crop Biotechnology, Ministry of Education, College of Life Science, Inner Mongolia University, Hohhot, Inner Mongolia 010021, PR China

2. Division of Biological Sciences, University of Missouri, Columbia, MO 65211, USA

3. Bayer’s Crop Science Division, Chesterfield, MO 63017, USA

4. Department of Horticulture, Michigan State University, East Lansing, MI 48823, USA

Abstract

AbstractHomoeologous 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.

Funder

National Natural Science Foundation of China

National Key Research and Development Program

Inner Mongolia Key Technology Research Plan

Inner Mongolia Natural Science Foundation

USDA-NIFA Hatch

USA National Science Foundation

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology

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