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首页> 外文期刊>Pakistan journal of botany >GENETIC DIVERSITY ANALYSIS OF BRASSICA NAPUS/BRASSICA CAMPESTRIS PROGENIES USING MICROSATELLITE MARKERS
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GENETIC DIVERSITY ANALYSIS OF BRASSICA NAPUS/BRASSICA CAMPESTRIS PROGENIES USING MICROSATELLITE MARKERS

机译:使用微卫星标记的Brassica Napus / Brassica Campestris Prensies的遗传多样性分析

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Genetic diversity and relationship of F2 segregating progenies of interspecific crosses between B. napus N-501/B.campestris C-118 were studied. A set of 90 genotypes (2 parental lines and their 88 F2 progenies) was characterizedseparately using 24 microsatellite or SSR markers to cover the diversity as broadly as possibly present in them. In initialscreening only 12 out of 24 SSR primers combination amplified DNA fragments, while the remaining 12 SSR primers didnot amplify DNA fragment therefore those 12 SSR molecular markers were not used for further analysis. The 12 SSRprimer combinations generated a total of 33 alleles, of that 32 were polymorphic loci, whereas only one was monomorphiclocus. Primers BRMS-19 and BRMS-40 were highly polymorphic producing 4 bands each. Primer Ra2-D04 was lesspolymorphic and it produced only one band. The proportion of polymorphic loci was 95.83% which indicates high geneticdiversity among the progenies. The average number of polymorphic alleles per locus was 2.66. The PIC values ranged from0.395 for primer Ra2-E03 to 0.726 for primer BRMS-019 with an average genetic diversity (PIC value) of 0.584 per locus.Seven primers showed PIC values above 0.5 (50%) indicating high genetic diversity in the studied plant materials. Pair-wisesimilarity indices among 90 genotypes ranged from 0.3 to 0.95. Dendrogram obtained through UPGMA clustering of F2progenies depicted eight main groups using similarity coefficient of 0.70. The progenies could be similar to their parents ifthey have the same banding patterns as that of the parents and could be distinguished from each other by the combination offragments which are repeatedly present in one progeny and absent in the other. Considerable genetic diversity has beenfound among the F2 segregating progenies and their parents using SSR markers thus, SSR analysis proved to be a usefultool.
机译:研究了B. Napus N-501 / B.campseStris C-118之间间隙横向的F2分离后代的遗传多样性和关系。使用24种微卫星或SSR标记的肝脏表征了一组90种基因型(2个父母线及其88个F2后代),以尽可能广泛地覆盖多样性。在初始筛选中仅为24个SSR引物组合组合扩增的DNA片段,而剩余的12SSR引物未吸收DNA片段,因此不使用那些12SSR的分子标记进行进一步分析。 12个SSRPRIMER组合产生了总共33个等位基因,其中32个是多态位置,而只有一个是单数卟啉。引物BRMS-19和BRMS-40是高度多态性产生4条带。引物Ra2-D04是不合因的,它仅生产一个带。多晶型基因座的比例为95.83%,这表明产后的高遗传性。每个基因座的平均多态等位基因数为2.66。用于引物BRMS-019的引物Ra2-E03至0.726的PIC值范围为0.395,具有0.584的平均遗传多样性(PIC值),每位基因座。综注于0.5(50%)表明高遗传多样性的PIC值学习植物材料。 90种基因型中的配对似体指数范围为0.3至0.95。通过F2PrOgeneies的UPGMA聚类获得的树枝图描绘了使用0.70的相似系数的八个主要组。这种后代可以与父母类似,如果它们具有与父母的绑扎图案相同,并且可以通过组合偏移彼此区分,其在一个后代中重复存在并且在另一个后部缺席。因此,使用SSR标记的F2分离后代和父母的遗传多样性相当大的遗传多样性因此,SSR分析被证明是一种使用。

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