Department of Botany and Microbiology, College of Science, King Saud University, Riyadh 11451, Kingdom of Saudi Arabia.
Saudi J Biol Sci. 2011 Jul;18(3):287-92. doi: 10.1016/j.sjbs.2011.03.001. Epub 2011 Mar 25.
In this study "RAPD" molecular marker was employed for the identification of Senna angustifolia, Senna acutifolia, Senna tora and Senna sophera. Total 32 decamer primers were screened in amplification with genomic DNA extracted from all species, of which 6 primers yielded species-specific reproducible bands. Out of 42 loci detected, the polymorphic, monomorphic and unique loci were 24, 2 and 16, respectively. Based on dendrogram and similarity matrix, 4 species were differentiated from each other and showed more divergence. Thus, this technique may prove and to contribute the identification of these species of Senna having similar morphology sold in the local markets.
本研究采用“RAPD”分子标记对狭叶番泻、尖叶番泻、扭肚泻和大孔番泻进行鉴定。从所有物种中提取基因组 DNA 进行扩增,筛选出 32 个十聚体引物,其中 6 个引物产生了具有物种特异性的可重复带。在检测到的 42 个位点中,多态性、单态性和独特性位点分别为 24、2 和 16。基于聚类图和相似性矩阵,这 4 种番泻属植物彼此分化,表现出更大的差异。因此,该技术可能有助于鉴定在当地市场上销售的形态相似的番泻属植物。