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Self-(in)compatibility inheritance and allele-specific marker development in yellow mustard (Sinapis alba)

Yellow mustard (Sinapis alba) has a sporophytic self-incompatibility reproduction system. Genetically stable self-incompatible (SI) and self-compatible (SC) inbred lines have recently been developed in this crop. Understanding the S haplotype of different inbred lines and the inheritance of the self...

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Autores principales: Zeng, Fangqin, Cheng, Bifang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3890562/
https://www.ncbi.nlm.nih.gov/pubmed/24482603
http://dx.doi.org/10.1007/s11032-013-9943-8
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author Zeng, Fangqin
Cheng, Bifang
author_facet Zeng, Fangqin
Cheng, Bifang
author_sort Zeng, Fangqin
collection PubMed
description Yellow mustard (Sinapis alba) has a sporophytic self-incompatibility reproduction system. Genetically stable self-incompatible (SI) and self-compatible (SC) inbred lines have recently been developed in this crop. Understanding the S haplotype of different inbred lines and the inheritance of the self-(in)compatibility (SI/SC) trait is very important for breeding purposes. In this study, we used the S-locus gene-specific primers in Brassica rapa and Brassica oleracea to clone yellow mustard S-locus genes of SI lines Y514 and Y1130 and SC lines Y1499 and Y1501. The PCR amplification results and DNA sequences of the S-locus genes revealed that Y514 carried the class I S haplotype, while Y1130, Y1499, and Y1501 had the class II S haplotype. The results of our genetic studies indicated that self-incompatibility was dominant over self-compatibility and controlled by a one-gene locus in the two crosses of Y514 × Y1499 and Y1130 × Y1501. Of the five S-locus gene polymorphic primer pairs, Sal-SLGI and Sal-SRKI each generated one dominant marker for the SI phenotype of Y514; Sal-SLGII and Sal-SRKII produced dominant marker(s) for the SC phenotype of Y1501 and Y1499; Sal-SP11II generated one dominant marker for Y1130. These markers co-segregated with the SI/SC phenotype in the F(2) populations of the two crosses. In addition, co-dominant markers were developed by mixing the two polymorphic primer pairs specific for each parent in the multiplex PCR, which allowed zygosity to be determined in the F(2) populations. The SI/SC allele-specific markers have proven to be very useful for the selection of the desirable SC genotypes in our yellow mustard breeding program. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11032-013-9943-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-38905622014-01-28 Self-(in)compatibility inheritance and allele-specific marker development in yellow mustard (Sinapis alba) Zeng, Fangqin Cheng, Bifang Mol Breed Article Yellow mustard (Sinapis alba) has a sporophytic self-incompatibility reproduction system. Genetically stable self-incompatible (SI) and self-compatible (SC) inbred lines have recently been developed in this crop. Understanding the S haplotype of different inbred lines and the inheritance of the self-(in)compatibility (SI/SC) trait is very important for breeding purposes. In this study, we used the S-locus gene-specific primers in Brassica rapa and Brassica oleracea to clone yellow mustard S-locus genes of SI lines Y514 and Y1130 and SC lines Y1499 and Y1501. The PCR amplification results and DNA sequences of the S-locus genes revealed that Y514 carried the class I S haplotype, while Y1130, Y1499, and Y1501 had the class II S haplotype. The results of our genetic studies indicated that self-incompatibility was dominant over self-compatibility and controlled by a one-gene locus in the two crosses of Y514 × Y1499 and Y1130 × Y1501. Of the five S-locus gene polymorphic primer pairs, Sal-SLGI and Sal-SRKI each generated one dominant marker for the SI phenotype of Y514; Sal-SLGII and Sal-SRKII produced dominant marker(s) for the SC phenotype of Y1501 and Y1499; Sal-SP11II generated one dominant marker for Y1130. These markers co-segregated with the SI/SC phenotype in the F(2) populations of the two crosses. In addition, co-dominant markers were developed by mixing the two polymorphic primer pairs specific for each parent in the multiplex PCR, which allowed zygosity to be determined in the F(2) populations. The SI/SC allele-specific markers have proven to be very useful for the selection of the desirable SC genotypes in our yellow mustard breeding program. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11032-013-9943-8) contains supplementary material, which is available to authorized users. Springer Netherlands 2013-09-22 2014 /pmc/articles/PMC3890562/ /pubmed/24482603 http://dx.doi.org/10.1007/s11032-013-9943-8 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Article
Zeng, Fangqin
Cheng, Bifang
Self-(in)compatibility inheritance and allele-specific marker development in yellow mustard (Sinapis alba)
title Self-(in)compatibility inheritance and allele-specific marker development in yellow mustard (Sinapis alba)
title_full Self-(in)compatibility inheritance and allele-specific marker development in yellow mustard (Sinapis alba)
title_fullStr Self-(in)compatibility inheritance and allele-specific marker development in yellow mustard (Sinapis alba)
title_full_unstemmed Self-(in)compatibility inheritance and allele-specific marker development in yellow mustard (Sinapis alba)
title_short Self-(in)compatibility inheritance and allele-specific marker development in yellow mustard (Sinapis alba)
title_sort self-(in)compatibility inheritance and allele-specific marker development in yellow mustard (sinapis alba)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3890562/
https://www.ncbi.nlm.nih.gov/pubmed/24482603
http://dx.doi.org/10.1007/s11032-013-9943-8
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