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Discovery and characterization of new microsatellite loci in Dipteryx alata Vogel (Fabaceae) using next-generation sequencing data

机译:利用下一代测序数据在Dipteryx alata Vogel(Fabaceae)中发现和表征新的微卫星基因座

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The use of next-generation sequencing (NGS) technologies provides a great volume of genome sequence data even for non-model species. The development of microsatellite markers using these data is a relatively quick and easy process. Dipteryx alata Vogel (Fabaceae) is an arboreal species from the Cerrado biome and is considered an important plant genetic resource. Here, we report the development of microsatellite markers for D. alata using NGS data. DNA samples from four individuals were sequenced using the Illumina MiSeq platform and high-quality reads were assembled into contigs of the D. alata genome sequence. Microsatellite regions were identified using the IMEX webserver and primer pairs were designed using the Primer3 software. The amplification settings for each locus were optimized. Fluorescent-labeled primers were developed and used to genotype individuals derived from three natural populations of D. alata. Fifty-four microsatellite regions were identified, from which 27 were elected to primer design. Among the amplified loci, 11 were polymorphic, with the number of alleles ranging from 2 to 10. The expected heterozygosity under Hardy-Weinberg Equilibrium (HWE) per locus varied from 0.191 to 0.807. Genotype and allele frequencies for all loci agreed with those expected under HWE and linkage disequilibrium was not significant for all pairs of loci. The probabilities of exclusion of paternity and of combined identity were equal to 0.993 and 5.65 x 10-8, respectively. The markers developed in this study are useful to several types of population genetic studies with D. alata and, eventually, for closely related species.
机译:下一代测序(NGS)技术的使用甚至为非模型物种提供了大量的基因组序列数据。利用这些数据开发微卫星标记是一个相对快速和容易的过程。 Dipteryx alata Vogel(Fabaceae)是Cerrado生物群落中的树栖物种,被认为是重要的植物遗传资源。在这里,我们使用NGS数据报告D. alata微卫星标记的发展。使用Illumina MiSeq平台对来自四个个体的DNA样品进行测序,并将高质量读段组装到D. alata基因组序列的重叠群中。使用IMEX Web服务器识别微卫星区域,并使用Primer3软件设计引物对。优化每个基因座的扩增设置。开发了荧光标记的引物,并将其用于对来自三个D. alata自然种群的个体进行基因分型。确定了54个微卫星区域,从中选择了27个进行引物设计。在扩增的基因座中,有11个是多态性,等位基因的数量在2到10之间。在每个位点的Hardy-Weinberg平衡(HWE)下预期的杂合度在0.191到0.807之间变化。所有基因座的基因型和等位基因频率与在HWE下预期的一致,连锁不平衡对所有基因座对都不显着。排除亲子关系和合并身份的概率分别等于0.993和5.65 x 10-8。在这项研究中开发的标记可用于几种与D. alata的种群遗传研究,并最终可用于密切相关的物种。

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