» Articles » PMID: 12807785

PrBn, a Major Gene Controlling Homeologous Pairing in Oilseed Rape (Brassica Napus) Haploids

Overview
Journal Genetics
Specialty Genetics
Date 2003 Jun 17
PMID 12807785
Citations 80
Authors
Affiliations
Soon will be listed here.
Abstract

Precise control of chromosome pairing is vital for conferring meiotic, and hence reproductive, stability in sexually reproducing polyploids. Apart from the Ph1 locus of wheat that suppresses homeologous pairing, little is known about the activity of genes that contribute to the cytological diploidization of allopolyploids. In oilseed rape (Brassica napus) haploids, the amount of chromosome pairing at metaphase I (MI) of meiosis varies depending on the varieties the haploids originate from. In this study, we combined a segregation analysis with a maximum-likelihood approach to demonstrate that this variation is genetically based and controlled mainly by a gene with a major effect. A total of 244 haploids were produced from F(1) hybrids between a high- and a low-pairing variety (at the haploid stage) and their meiotic behavior at MI was characterized. Likelihood-ratio statistics were used to demonstrate that the distribution of the number of univalents among these haploids was consistent with the segregation of a diallelic major gene, presumably in a background of polygenic variation. Our observations suggest that this gene, named PrBn, is different from Ph1 and could thus provide complementary information on the meiotic stabilization of chromosome pairing in allopolyploid species.

Citing Articles

Unambiguous chromosome identification reveals the factors impacting irregular chromosome behaviors in allotriploid AAC Brassica.

Cao Y, Xu J, Wang M, Gao J, Zhao Z, Li K Theor Appl Genet. 2024; 137(10):245.

PMID: 39365356 DOI: 10.1007/s00122-024-04734-6.


Contribution of homoeologous exchange to domestication of polyploid Brassica.

Wang T, van Dijk A, Zhao R, Bonnema G, Wang X Genome Biol. 2024; 25(1):231.

PMID: 39192349 PMC: 11350971. DOI: 10.1186/s13059-024-03370-z.


Genetic diversification of allohexaploid Brassica hybrids (AABBCC) using a fertile octoploid with excessive C genome set (AABBCCCC).

Shinke T, Yamazaki A, Nakamura S, Kudoh H, Hosokawa M Planta. 2024; 260(3):71.

PMID: 39136783 DOI: 10.1007/s00425-024-04497-w.


Separating phases of allopolyploid evolution with resynthesized and natural .

Duan T, Sicard A, Glemin S, Lascoux M Elife. 2024; 12.

PMID: 38189348 PMC: 10945474. DOI: 10.7554/eLife.88398.


The genetic consequences of range expansion and its influence on diploidization in polyploids.

Booker W, Schrider D bioRxiv. 2023; .

PMID: 37905020 PMC: 10614938. DOI: 10.1101/2023.10.18.562992.


References
1.
Sharpe A, Parkin I, Keith D, Lydiate D . Frequent nonreciprocal translocations in the amphidiploid genome of oilseed rape (Brassica napus). Genome. 1995; 38(6):1112-21. DOI: 10.1139/g95-148. View

2.
Masterson J . Stomatal size in fossil plants: evidence for polyploidy in majority of angiosperms. Science. 1994; 264(5157):421-4. DOI: 10.1126/science.264.5157.421. View

3.
Wu R, Li B, Wu S, Casella G . A maximum likelihood-based method for mining major genes affecting a quantitative character. Biometrics. 2001; 57(3):764-8. DOI: 10.1111/j.0006-341x.2001.00764.x. View

4.
Sanchez-Moran E, Benavente E, Orellana J . Analysis of karyotypic stability of homoeologous-pairing (ph) mutants in allopolyploid wheats. Chromosoma. 2001; 110(5):371-7. DOI: 10.1007/s004120100156. View

5.
Shaw P, Moore G . Meiosis: vive la difference!. Curr Opin Plant Biol. 1999; 1(6):458-62. DOI: 10.1016/s1369-5266(98)80035-6. View