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RAPD 标记在 n=9 的野生芸薹属种内和种间水平的遗传有效性。

Genetic validity of RAPD markers at the intra- and inter-specific level in wild Brassica species with n=9.

机构信息

Department of Plant Breeding Research, Swedish University of Agricultural Sciences, S-268 31, Svalöv, Sweden.

出版信息

Theor Appl Genet. 1996 Jul;93(1-2):9-14. doi: 10.1007/BF00225720.

Abstract

The sequence homology of co-migrating RAPD markers within a genus, across species, and among populations of a species was investigated. DNA was isolated from ten wild Brassica species with n=9 and the RAPD patterns were established using three random primers. Five RAPD markers which appeared to be characteristic for the n=9 species (genus level), four markers which appeared to be species specific, and one population-specific marker were isolated from agarose gels and hybridized to the RAPD profiles of the ten Brassica species. Two RAPD markers were cloned for comparison with gel-isolated RAPD fragment probes in hybridization experiments. Non-specific and background hybridization, occurring when gel-isolated fragments were used as probes, disappeared when cloned fragments were used. A total of 250 RAPD-marker hybridizations were scored according to visual presence or absence in a gel lane. All except three markers hybridized as expected, resulting in an error rate of 1.2%. The deviating results included a lack of hybridization although a band was visible in the gel, a length polymorphism for one marker, and a dual hybridization signal for two single-band markers.

摘要

本研究旨在调查同迁移 RAPD 标记在属内、种间和种内群体间的序列同源性。从 10 种野生 Brassica 物种(n=9)中提取 DNA,使用 3 个随机引物建立 RAPD 图谱。从琼脂糖凝胶中分离出 5 个似乎是 n=9 种(属水平)特有、4 个似乎是种特异、1 个种群特异的 RAPD 标记,并将其与 10 种 Brassica 物种的 RAPD 图谱进行杂交。为了与杂交实验中的凝胶分离 RAPD 片段探针进行比较,克隆了 2 个 RAPD 标记。当使用凝胶分离片段作为探针时,会发生非特异性和背景杂交,而当使用克隆片段时,这种情况就会消失。根据凝胶泳道中是否存在可视带,共对 250 个 RAPD 标记杂交进行了评分。除了 3 个标记外,所有标记都按预期进行杂交,错误率为 1.2%。偏离的结果包括尽管在凝胶中可见带但没有杂交、一个标记存在长度多态性以及两个单带标记存在双重杂交信号。

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