The genetic diversities of cytochrome b, COI, ND2, ND4, 12S rRNA and 16S rRNA genes of mtDNA were analyzed by PCR-SSCP method among these individuals, and variable sites were found through sequencing analysis which led to the diversities.

• 通过PCR-SSCP 及DNA 测序的方法对这些品种(共468 个体)线粒体DNA 编码区的Cytb、COI、ND2、ND4、12S rRNA 和16SrRNA 基因设计特异性引物进行多态性分析,并通过测序分析找出了导致多态的变异位点。