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Novel microsatellite markers suitable for genetic studies in Polyporus umbellatus (Polyporales, Basidiomycota)

机译:新型微卫星标记适用于多肽umbellatus(多脂素,盆西)的基因研究

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Polyporus umbellatus, known as Zhuling in China, is a well-known and important medicinal fungus in Asia. Although P. umbellatus is highly valued for its medicinal properties, the expressed sequence based (genetic) markers are unknown. High-throughput transcriptome sequencing provides large amounts of transcriptome data for gene discovery and the development of molecular markers. In this study, all 38,444 unigenes were used to screen the SSR loci. A total of 1527 primer pairs were designed for marker development. Tri-nucleotide repeat motifs were the most abundant type, with a frequency of 47.4%, followed by mono- (28.5%), di- (21.1%), tetra- (0.16%), hexa- (0.1%) and penta-nucleotide repeat motifs (0.05%). A total of 50 primer pairs were synthesized, of which 31(62%) yielded PCR amplification products. Eight individuals were used to examine amplifications and polymorphisms for all 50 loci. In eight P. umbellatus accessions, eight markers were polymorphic. To describe the genetic diversity and genetic relationship of P. umbellatus, the genotypes of 42 accessions representing diverse wild genotypes of P. umbellatus were analyzed. The number of alleles per locus varied from 7 to 13 alleles, and the genetic diversity values ranged from 0.345 to 0.785. We performed genetic diversity analysis using these 8 polymorphic markers. A UPGMA dendrogram was constructed based on Jaccard's similarity coefficients, revealing distinct clusters among the 42 accessions. This comprehensive set of genic SSR markers developed in our study is powerful and suitable for genetic analysis. (C) 2015 Elsevier Ltd. All rights reserved.
机译:在中国称为zhuling的Polyporus Umbellatus是亚洲的着名和重要的药用真菌。虽然P.Mubellatus高度重视其药用特性,但基于表达的序列(遗传)标记是未知的。高通量转录组测序为基因发现和分子标记的发育提供了大量的转录组数据。在这项研究中,所有38,444个unigenes都用于筛选SSR基因座。共有1527个底漆对进行标记开发。三核苷酸重复基序是最丰富的类型,频率为47.4%,其次是单 - (28.5%),二 - (21.1%),四(0.16%),六升(0.1%)和五角洲 - 核苷酸重复基序(0.05%)。合成总共50个引物对,其中31(62%)得到PCR扩增产物。八个人用于检查所有50个基因座的扩增和多态性。在八个P.Mubellatus access中,八个标记是多态的。为了描述P.Mubellatus的遗传多样性和遗传关系,分析了代表P.Mubellatus的不同野生基因型的42种遗传学的基因型。每个基因座的等位基因数量从7到13等位基因变化,遗传分集值范围为0.345至0.785。我们使用这8种多态标记进行了遗传多样性分析。基于Jaccard的相似性系数构建了UPGMA树木图,在42种附加方案中揭示了不同的簇。我们研究中开发的这一综合基因SSR标记是强大的,适合遗传分析。 (c)2015 Elsevier Ltd.保留所有权利。

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