Department of Crop Science, North Carolina State University, 27695-7620, Raleigh, NC.
Theor Appl Genet. 1994 Jan;87(6):689-96. doi: 10.1007/BF00222894.
Isozyme analysis is a valuable tool for determining genetic relationships among breeding lines and populations. The recently developed DNA technologies which can assay a greater proportion of the plant genome are providing a plentiful array of additional genomic markers. The objective of this research was to compare random amplified polymorphic DNA (RAPD) versus isozyme-based estimation of relationships among 24 accessions of a hexaploid wild oat, Avena sterilis L. The accessions were evaluated for variation in 23 enzyme systems and by 21 10-mer primers. A total of 77 polymorphic isozyme bands and 115 polymorphic RAPD bands were observed. Two matrices of genetic distances were estimated based on band presence/ absence. These matrices were subsequently utilized in cluster analysis and principal coordinate analysis. Both isozymes and RAPDs were proficient at distinguishing between the 24 accessions. The correspondence between the elements of both distance matrices was moderate (r=0.36**). Nevertheless, the overall representation of relationships among accessions by cluster analysis and ordination was in considerable agreement. The two techniques contrasted most notably in pair-by-pair comparisons of relationships. RAPD analysis resulted in a more definitive separation of clusters of accessions. The most significant impact of the DNA-based markers probably will be the more accurate determination of relationships between accessions that are too close to be accurately differentiated by isozymes.
同工酶分析是确定育种系和群体遗传关系的一种有价值的工具。最近开发的 DNA 技术可以检测植物基因组的更大比例,为提供大量额外的基因组标记提供了可能。本研究的目的是比较随机扩增多态性 DNA(RAPD)与同工酶对 24 个六倍体野生燕麦 Avena sterilis L. 系的亲缘关系的估计。对 23 种酶系统和 21 种 10 聚体引物的变异进行了评估。共观察到 77 条多态同工酶带和 115 条多态 RAPD 带。基于带的存在/不存在,估计了两个遗传距离矩阵。随后将这些矩阵用于聚类分析和主坐标分析。同工酶和 RAPD 都能很好地区分 24 个系。两个距离矩阵的元素之间具有中等的对应关系(r=0.36**)。尽管如此,聚类分析和排序对系之间关系的整体表现还是相当一致的。这两种技术的对比在关系的两两比较中最为明显。RAPD 分析导致聚类的系更明确地分离。DNA 标记的最大影响可能是更准确地确定由于太接近而不能通过同工酶准确区分的系之间的关系。