Cambridge Laboratory, Colney Lane, NR4 7UJ, Norwich, UK.
Theor Appl Genet. 1992 Aug;84(5-6):567-72. doi: 10.1007/BF00224153.
An evaluation was made of the use of random amplified polymorphic DNA (RAPD) as a genetic marker system in wheat. Reproducible amplification products were obtained from varietal, homozygous single chromosome recombinant line and wheat/alien addition line genomic DNA with selected primers and rigorously optimized reaction conditions. Factors influencing the RAPD patterns are DNA concentration, Mg(2+) concentration, polymerase concentration and denaturing temperature. In wheat, the non-homoeologous, non-dose responsive and dominant behaviour of RAPD products devalues their use as genetic markers for the construction of linkage maps, and the high probability that the amplified fragments derive from repetitive DNA limits their use as a source of conventional RFLP probes. However, RAPD markers will most certainly find many applications in the analysis of genotypes where single chromosomes or chromosome segments are to be manipulated.
评价了随机扩增多态性 DNA(RAPD)作为小麦遗传标记系统的应用。使用选定的引物和严格优化的反应条件,从品种、纯合单染色体重组系和小麦/外源添加系基因组 DNA 中获得了可重复的扩增产物。影响 RAPD 图谱的因素有 DNA 浓度、Mg(2+)浓度、聚合酶浓度和变性温度。在小麦中,RAPD 产物的非同源、非剂量反应和显性行为降低了它们作为连锁图谱构建遗传标记的用途,而扩增片段来源于重复 DNA 的高概率限制了它们作为常规 RFLP 探针来源的用途。然而,RAPD 标记在分析需要操作单条染色体或染色体片段的基因型时,肯定会有许多应用。