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作 者:曾建[1] 张利[1] 凡星[1] 张春[1] 张海琴[1] 周永红[1]
机构地区:[1]四川农业大学小麦研究所,四川都江堰611830
出 处:《四川农业大学学报》2006年第4期369-374,共6页Journal of Sichuan Agricultural University
基 金:国家自然科学基金项目(编号:30470135和30270099);教育部长江学者和创新团队发展计划(编号:IRT0453)
摘 要:通过PCR产物克隆测序和直接产物测序的方法对禾本科小麦族仲彬草属10个物种的rDNA内转录间隔区(ITS)及5.8SrDNA进行了序列测定和系统发育分析。结果表明:该属植物ITS区直接产物测序与克隆测序存在较大差异,克隆测序序列反映的系统发育关系与形态学、地理分布、细胞学、分子标记分析结果基本一致。因此,采用克隆测序的方法对仲彬草属植物系统发育分析比直接测序方法更为可靠。The results of direct sequencing of PCR products and sequencing by cloning PCR products of the internal transcribed spacers and the 5.8S coding regions of nuclear ribosomal DNA in Kengyilia were compared and phylogenetieally analyzed. The results show that ITS sequences are of existed differences between the direct sequencing of PCR products and sequencing by cloning PCR products. The phylogenetic relationship in Kengyilia species based on sequences by cloning PCR products is consistent with the analysis of morphology, geographical distribution, cytology and molecular markers. Therefore, phylogenetic analysis carried out by sequencing of cloning PCR products is more credible than that inferred from direct sequencing of PCR products.
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