【摘要】 [目的]进行红锥、白椎、大叶栎3个树种的分子鉴定研究。[方法]利用ISSR-PCR方法构建红锥(Castanopsis hystrix)、白椎(Cas-tanopsis carlesii Hayata)、大叶栎(Quercus griffithii Hook)3个树种的DNA指纹图谱,根据各个体的Nei氏遗传距离矩阵,利用UPGMA法进行聚类分析。[结果]从50个ISSR引物中筛选出6个多态性引物用于ISSR-PCR扩增,共扩增出86条不同DNA带,平均每个引物扩增的DNA带的数目为10.75条,多态性条带数目为53条,占总条带数的61.2%。其中,有5个引物可扩增出差异条带和特异条带,能准确地鉴定上述3个树种。应用DPS软件计算供试材料的遗传距离界于0.166 67～0.809 52之间,平均为0.563 57。[结论]ISSR-PCR方法可以解决红锥、白锥、大叶栎的鉴定问题。更多还原

【Abstract】 [Objective] This research aimed to develop molecular identification method for Castanopsis hystrix,Castanopsis carlesii and Quercus griffithii.[Method] DNA fingerprints of C.hystrix,C.carlesii and Q.griffithii were established using ISSR-PCR method.Cluster Analysis was carried out using UPGMA method based on Nei’s genetic distances among each individual.[Result] Six polymorphic primers were selected from 50 ISSR primers for ISSR-PCR amplification,and totally 86 discernible DNA bands were amplified with 53 polymorphic bands,accounting for 61.2% of the total.The average number of DNA bands amplified by each primer was 10.75.Specifically,totally 5 primers had amplified differential bands and specific bands,which were able to accurately identify C.hystrix,C.carlesii and Q.griffithii.As calculated by DPS v3.01 software,the genetic distances among test materials were ranged from 0.166 67 to 0.809 52,with an average of 0.563 57.[Conclusion] ISSR-PCR method can be used to identify C.hystrix,C.carlesii and Q.griffithii effectively.更多还原