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从甘蓝型油菜(油菜)大小分级基因组文库中分离的简单重复序列(SSR)的丰度和特征。

Abundance and characterization of simple-sequence repeats (SSRs) isolated from a size-fractionated genomic library of Brassica napus L. (rapeseed).

机构信息

USDA-ARS, Plant Genetic Resources Conservation Unit, University of Georgia, 30223-1797, Griffin, GA, USA.

出版信息

Theor Appl Genet. 1995 Jul;91(2):206-11. doi: 10.1007/BF00220879.

Abstract

A size-fractionated library of Brassica napus L. (rapeseed), composed of 15000 clones, was screened for the presence of GA-, CA-, and GATA-simple-sequence repeats (SSRs). GA-SSRs were four- and five-fold more abundant than CA- and GATA-SSRs, respectively, and present at a frequency of approximately one SSR for every 100 kb of DNA. Following the sequencing of 124 positive clones, primer pairs were designed and evaluated for seven selected SSRs. Products were amplified in an array of individuals of B. napus, B. oleracea and B. rapa, demonstrating that the seven SSRs were conserved among species. Two SSRs were polymorphic. Among 11 accessions, the dinucleotide (GA)-repeat, B.n.9A, yielded 12 fragments, while the tetranucleotide-repeat (GATA), B.n.6A2, revealed two fragments. Automated, fluorescence-based detection of polyacrylamide gels has been employed to simultaneously increase throughput, reduce unit cost, improve analytical resolution, and expedite data acquisition of SSR analysis. Though initial financial investment and technical capabilities may prevent some from directly employing our documented approach, SSR analysis warrants further investigation as a tool in genetic studies for enhancing both the conservation and utilization of genetic resources.

摘要

甘蓝型油菜(油菜)的大小分级文库由 15000 个克隆组成,用于筛选 GA-、CA- 和 GATA-简单重复序列(SSR)的存在。GA-SSR 的丰度分别比 CA-和 GATA-SSR 高四到五倍,频率约为每 100kbDNA 有一个 SSR。在对 124 个阳性克隆进行测序后,为七个选定的 SSR 设计并评估了引物对。在油菜、甘蓝和白菜的一系列个体中扩增了产物,证明了这七个 SSR 在物种间是保守的。两个 SSR 是多态的。在 11 个品系中,二核苷酸(GA)-重复 B.n.9A 产生 12 个片段,而四核苷酸重复 B.n.6A2 显示出两个片段。自动、基于荧光的聚丙烯酰胺凝胶检测已被用于同时提高通量、降低单位成本、提高分析分辨率,并加快 SSR 分析的数据采集。尽管初始财务投资和技术能力可能会阻止一些人直接采用我们记录的方法,但 SSR 分析作为遗传研究中增强遗传资源保护和利用的工具值得进一步研究。

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