首页> 外文期刊>BMC research notes >The coding region of the UFGT gene is a source of diagnostic SNP markers that allow single-locus DNA genotyping for the assessment of cultivar identity and ancestry in grapevine (Vitis vinifera L.)
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The coding region of the UFGT gene is a source of diagnostic SNP markers that allow single-locus DNA genotyping for the assessment of cultivar identity and ancestry in grapevine (Vitis vinifera L.)

机译:UFGT基因的编码区是诊断SNP标记的来源,可通过单基因座DNA基因分型来评估葡萄的品种同一性和血统(葡萄)。

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Background Vitis vinifera L. is one of society’s most important agricultural crops with a broad genetic variability. The difficulty in recognizing grapevine genotypes based on ampelographic traits and secondary metabolites prompted the development of molecular markers suitable for achieving variety genetic identification. Findings Here, we propose a comparison between a multi-locus barcoding approach based on six chloroplast markers and a single-copy nuclear gene sequencing method using five coding regions combined with a character-based system with the aim of reconstructing cultivar-specific haplotypes and genotypes to be exploited for the molecular characterization of 157 V. vinifera accessions. The analysis of the chloroplast target regions proved the inadequacy of the DNA barcoding approach at the subspecies level, and hence further DNA genotyping analyses were targeted on the sequences of five nuclear single-copy genes amplified across all of the accessions. The sequencing of the coding region of the UFGT nuclear gene (UDP-glucose: flavonoid 3-0-glucosyltransferase, the key enzyme for the accumulation of anthocyanins in berry skins) enabled the discovery of discriminant SNPs (1/34?bp) and the reconstruction of 130 V. vinifera distinct genotypes. Most of the genotypes proved to be cultivar-specific, and only few genotypes were shared by more, although strictly related, cultivars. Conclusion On the whole, this technique was successful for inferring SNP-based genotypes of grapevine accessions suitable for assessing the genetic identity and ancestry of international cultivars and also useful for corroborating some hypotheses regarding the origin of local varieties, suggesting several issues of misidentification (synonymy/homonymy).
机译:背景葡萄(Vitis vinifera L.)是社会上最重要的农作物之一,具有广泛的遗传变异性。基于流变学特征和次生代谢产物识别葡萄基因型的困难促使人们开发了适于实现多种遗传鉴定的分子标记。研究结果在这里,我们提出了一种基于六个叶绿体标记的多位点条形码编码方法与一个使用五个编码区结合基于字符的系统的单拷贝核基因测序方法的比较,目的是重建特定品种的单倍型和基因型可用于157个酿酒葡萄种的分子鉴定。对叶绿体靶区域的分析证明了在亚种水平上DNA条形码方法的不足,因此进一步的DNA基因分型分析针对的是在所有种质中扩增的五个核单拷贝基因的序列。 UFGT核基因编码区(UDP-葡萄糖:类黄酮3-0-葡萄糖基转移酶,是花色苷在浆果皮中积累的关键酶)的测序使发现有区别的SNP(1 / 34bp)成为可能。 130 V. vinifera不同基因型的重组。大多数基因型被证明是特定品种的,只有少数基因型与更多(尽管严格相关)的品种共享。结论总体而言,该技术成功地推论了基于SNP的葡萄品种的基因型,适合评估国际品种的遗传同一性和祖先,也可用于证实有关本地品种起源的某些假设,提示了一些错误识别的问题(同义词/同名)。

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