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Investigation of Genetic Diversity in Afghan Bread Wheat Genotypes Using SSR and AFLP Markers

机译:使用SSR和AFLP标记调查阿富汗面包小麦基因型遗传多样性

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摘要

Genetic diversity assessment is the principle component for conservation and characterization of germplasm. Genetic diversity study of Afghan bread wheat genotypes is a first step to identify and to select high performance genotypes and distribute to wheat breeding programs. The main objective of this study is to investigate of genetic diversity in 35 Afghan bread wheat genotypes by using Simple Sequence Repeat (SSR) and Amplified Fragment Length Polymorphism (AFLP) markers. DNA extraction according to Cetyl Trimethyl Ammonium Bromide (CTAB) method was conducted and the total genomic DNA was isolated from each variety. Sixty-four SSR primer markers were used and eighteen EcoRI+(N)/MseI+(N) primer combinations with their primer sequences were used for selective polymerase chain reaction (PCR) amplification. Every SSR and AFLP fragment was scored as present (1) or absent (0) within all genotypes under study. Marker/ Value ratio of pairwise genetic distance between genotypes according to the SSRs data was from 0.508 to 0.691 with an average distance of 0.599. Relatively different grouping pattern in comparison to AFLP data observed through cluster analysis. Both types of molecular markers (AFLP and SSR) used in this research proved to be suitable for investigating genetic diversity in the genotypes of Afghan bread wheat, however, AFLP markers gave better view of genetically relationships among genotypes than the SSR markers. The grouping generated by AFLP data showed a special agreement with the origin regions of genotypes (Ariana-07 and Mazar-99 originating from the north of Afghanistan, Lalmi-03 and Kabul-02. Large number of DNA bands identified with AFLP markers might provide a better estimation of genetic similarity than those of SSR markers.
机译:遗传多样性评估是种质保护和表征的原则组分。阿富汗面包小麦基因型的遗传多样性研究是识别和选择高性能基因型并分配给小麦育种计划的第一步。本研究的主要目的是通过使用简单的序列重复(SSR)和扩增的片段长度多态性(AFLP)标记来探讨35阿富汗面包小麦基因型中的遗传多样性。进行根据十六烷基三甲基溴化物(CTAB)方法的DNA提取,并从各种各样分离总基因组DNA。使用六十四个SSR引物标记物,并使用具有其引物序列的十八型EcoRI +(N)/ mSEI +(n)底漆组合用于选择性聚合酶链反应(PCR)扩增。每个SSR和AFLP片段都在研究中的所有基因型内被评定为现有(1)或缺席(0)。根据SSRS数据的基因型之间的成对遗传距离的标记/值比为0.508至0.691,平均距离为0.599。与通过聚类分析观察到的AFLP数据相对不同的分组模式。本研究中使用的两种类型的分子标记(AFLP和SSR)被证明是适合于研究阿富汗面包小麦的基因型中的遗传多样性,然而,AFLP标记物在基因型中的基因关系方面比SSR标记更好地看作遗传关系。 AFLP数据产生的分组显示了与基因型的起源区域特别协议(Ariana-07和来自阿富汗北部的Ariana-07和Mazar-99,Lalmi-03和Kabul-02。用AFLP标记鉴定的大量DNA带可能提供更好地估计遗传相似性比SSR标记物。

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