Dept. of Crop Production, University of Helsinki, SF-00710, Helsinki, Finland.
Plant Cell Rep. 1993 Jan;12(2):107-9. doi: 10.1007/BF00241944.
The identification of somatic hybrids between Solanum tuberosum and S. brevidens can be carried out using polymerase chain reaction (PCR) and arbitrary 10-mer primers to generate random amplified polymorphic DNA (RAPD) markers. Five commercial primers have been tested. Each primer directed the amplification of a genome-specific "fingerprint" for the fusion parents and S. brevidens. The size of the amplified DNA fragments ranged from 100 to 1800 base pairs. The somatic hybrids showed a combination of the parental banding profiles with four of the five primers surveyed, whereas regenerants from one of the parents had the same or a similar banding pattern to that of the parent. Thus RAPD markers provide a quick, simple and preliminary screening method for putative somatic hybrids.
利用聚合酶链反应(PCR)和任意的 10 -mer 引物,可以鉴定出马铃薯和短柄野芝麻之间的体细胞杂种。已经测试了 5 种商业引物。每个引物都针对融合亲本和短柄野芝麻的基因组特异性“指纹”进行扩增。扩增 DNA 片段的大小范围从 100 到 1800 个碱基对。体细胞杂种表现出 5 个调查引物中的 4 个亲本带型的组合,而来自一个亲本的再生体具有与亲本相同或相似的带型。因此,RAPD 标记为潜在的体细胞杂种提供了一种快速、简单和初步的筛选方法。