2009Journal of Pharmaceutical and Biomedical SciencesRequires access

Genetic diversity of parental lines of rapeseed hybrids based on SSR and SRAP markers.

Zu-meng TAN, Yunchang Li, Qiong Hu, Mei DeSheng, Yusong Xu, Ying-de LI

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Abstract

The genetic diversity of 49 parental lines used for hybrid production and breeding in Brassica napus L.and 2 related species was studied by SSR and SRAP markers, and the results of these two maker systems were compared.One hundred and ninety-four polymorphic fragments were detected using 45 SSR primer pairs, with an average number of polymorphic fragments per primer pair of 4.3, whereas 197 polymorphic fragments were detected using 25 SRAP primer pairs, with an average number of polymorphic fragments per primer pair of 7.9.The 51 lines could be divided into 5 groups based on either SSR or SRAP markers by UPGMA cluster analysis.The main maintainer lines and restorer lines of Polima cytoplasmic male sterility(CMS) were classified into the same group but different sub-groups.The groups classified by SRAP markers were more in accord with pedigree information than that by SSR markers.The SRAP markers were more effective in genetic analysis of closely related lines.The genetic distance calculated based on SRAP markers was larger than that on SSR markers.There was difference between the genetic diversity evaluated by SRAP and SSR markers, even though the same number of polymorphic fragments was used for evaluation.This difference may be caused by different numbers of variation alleles of the same gene detected by different primer sequences.

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The genetic diversity of 49 parental lines used for hybrid production and breeding in Brassica napus L.and 2 related species was studied by SSR and SRAP markers, and the results of these two maker systems were compared.One hundred and ninety-four polymorphic fragments were detected using 45 SSR primer pairs, with an average number of polymorphic fragments per primer pair of 4.3, whereas 197 polymorphic fragments were detected using 25 SRAP primer pairs, with an average number of polymorphic fragments per primer pair of 7.9.The 51 lines could be divided into 5 groups based on either SSR or SRAP markers by UPGMA cluster analysis.The main maintainer lines and restorer lines of Polima cytoplasmic male sterility(CMS) were classified into the same group but different sub-groups.The groups classified by SRAP markers were more in accord with pedigree information than that by SSR markers.The SRAP markers were more effective in genetic analysis of closely related lines.The genetic distance calculated based on SRAP markers was larger than that on SSR markers.There was difference between the genetic diversity evaluated by SRAP and SSR markers, even though the same number of polymorphic fragments was used for evaluation.This difference may be caused by different numbers of variation alleles of the same gene detected by different primer sequences.

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Available abstract

The genetic diversity of 49 parental lines used for hybrid production and breeding in Brassica napus L.and 2 related species was studied by SSR and SRAP markers, and the results of these two maker systems were compared.One hundred and ninety-four polymorphic fragments were detected using 45 SSR primer pairs, with an average number of polymorphic fragments per primer pair of 4.3, whereas 197 polymorphic fragments were detected using 25 SRAP primer pairs, with an average number of polymorphic fragments per primer pair of 7.9.The 51 lines could be divided into 5 groups based on either SSR or SRAP markers by UPGMA cluster analysis.The main maintainer lines and restorer lines of Polima cytoplasmic male sterility(CMS) were classified into the same group but different sub-groups.The groups classified by SRAP markers were more in accord with pedigree information than that by SSR markers.The SRAP markers were more effective in genetic analysis of closely related lines.The genetic distance calculated based on SRAP markers was larger than that on SSR markers.There was difference between the genetic diversity evaluated by SRAP and SSR markers, even though the same number of polymorphic fragments was used for evaluation.This difference may be caused by different numbers of variation alleles of the same gene detected by different primer sequences.

Key concepts: Biology, UPGMA, Genetic diversity, Genetics, Hybrid, Primer (cosmetics), Software maintainer, Genetic marker

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Genetic diversity of parental lines of rapeseed hybrids based on SSR and SRAP markers. — Research Paper | ScholarLens