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Development of SSR markers from Musa balbisiana for genetic diversity analysis among Thai bananas

机译:开发芭蕉(Musa balbisiana)SSR标记用于泰国香蕉遗传多样性分析

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Bananas in Thailand have been surveyed by our team to be at least 140 cultivars in the plantations, 10 wild species and, 4 introduced species. To characterize the genetic relationship of species and cultivars, a set of novel SSR markers was developed. Totaling 53 clones containing SSR motifs were isolated from SSR-enriched library of wild Musa balbisiana Colla 'Tani' (BB). Selected positive clones were used to design 28 primer pairs for amplification of 12 wild and 82 cultivar accessions with genome designations AA, AB, AAA, AAB, ABB, and BBB. These SSR markers loci were homology searched to the banana genomes to map their locations. The seven-sets multiplex PCR approach using four fluorescent-labeled universal primers were utilized for cost effectiveness. Capillary fragment analysis yielded the accurate size of amplicons for evaluation of particular patterns for each cultivar. Phylogram and Structure analysis presented the specific genotype of genome groups (A and B genotypes, polyploid hybrid genomes) and cultivar groups. By A:B specific alleles ratio, accurate genome designations of hybrids can be determined. Additionally, a marker, characterized to be partial plastid ycf2 gene, indicated the maternal identification of hybrid cultivars. One SSR marker was also preliminary tested with some wild species and advised to be the candidate fingerprinting marker for species identification. In conclusion, SSR marker sets developed here proved their exploitation in detailed identity and relationship of cultivated bananas, which would be useful for genetic conservation and ongoing breeding programs in Thailand and other areas.
机译:我们的团队对泰国的香蕉进行了调查,得出他们的种植园中至少有140个品种,有10种野生物种和4种引进物种。为了表征物种和品种的遗传关系,开发了一套新颖的SSR标记。从富集了野生野生芭蕉科(Mus balbisiana)Colla'Tani'(BB)的SSR的库中分离出总共53个含有SSR主题的克隆。选定的阳性克隆用于设计28个引物对,用于扩增12个野生和82个品种,基因组名称为AA,AB,AAA,AAB,ABB和BBB。将这些SSR标记基因座与香蕉基因组进行同源搜索以定位它们的位置。使用七套多重PCR方法(使用四种荧光标记的通用引物)可提高成本效益。毛细管片段分析产生了准确的扩增子大小,用于评估每个品种的特定模式。文字和结构分析显示了基因组组(A和B基因型,多倍体杂种基因组)和品种组的特定基因型。通过A:B特定等位基因比率,可以确定杂种的准确基因组名称。另外,特征在于部分质体ycf2基因的标记表明母本鉴定了杂交品种。还对一些野生物种进行了一种SSR标记的初步测试,建议将其用作进行物种鉴定的候选指纹标记。总之,这里开发的SSR标记集证明了它们在栽培香蕉的详细身份和关系上的开发利用,这对于泰国和其他地区的基因保护和正在进行的育种计划很有用。

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