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Molecular tools for utilization of mitochondrial diversity in faba bean (Vicia faba)

机译:利用蚕豆中线粒体多样性的分子工具

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We performed in silico PCR analyses utilizing complete mitochondrial (mtDNA) genome sequences of faba bean (Vicia faba) and two related species, Vigna angularis and Vigna radiata, currently available in GenBank, to infer whether 15 published universal primer pairs for amplification of all 14 cis-spliced introns in genes of NADH subunits (nad genes) are suitable for V. faba and related species. Then, we tested via PCR reactions whether seven out of 15 primer pairs would generate PCR products suitable for further manipulation in 16 genotypes of V. faba representing all botanical varieties of this species (major, minor, equina and subsp. paucijuga) of various levels of improvement (traditional and improved cultivars) originating from Europe, Africa, Asia and south America. We provide new PCR primers for amplification of nad1 intron 2/3 in V. faba, and demonstrate intraspecific variability in primary nucleotide sequences at this locus. Based on outcomes of both in silico predictions and PCR amplification, we report a set of PCR primers for amplification of five introns in nad genes that are promising molecular tools for future phylogeographic and other studies in this species for which unambiguous data on wild ancestors, centre of origin and domestication are lacking. [Projekat Ministarstva nauke Republike Srbije, br. 173005]
机译:我们利用蚕豆(Vicia faba)和目前在GenBank中可用的两个相关物种Vigna angularis和Vigna radiata的完整线粒体(mtDNA)基因组序列进行计算机PCR分析,以推断是否有15种已公开的通用引物对用于扩增全部14种NADH亚基基因(nad基因)中的顺式剪接内含子适用于蚕豆和相关种。然后,我们通过PCR反应测试了15个引物对中是否有7个会产生适合进一步处理代表该物种所有植物品种(主要,次要,马和亚种paucijuga)的16种基因型的V. faba的PCR产品来自欧洲,非洲,亚洲和南美的改良(传统和改良品种)。我们提供了新的PCR引物,用于在蚕豆中扩增nad1内含子2/3,并在该基因座处证明了主要核苷酸序列的种内变异性。基于计算机模拟预测和PCR扩增的结果,我们报告了一套PCR引物,用于扩增nad基因中的五个内含子,这些引物是该物种未来系统谱学和其他研究的有希望的分子工具,有关野生祖先,中心的明确数据缺乏起源和驯化。 [Projekat Ministarstva nauke Republike Srbije,br。 173005]

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