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不同产区麦冬、山麦冬rDNA-ITS序列分析

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利用特异性引物进行PCR扩增和克隆、测定不同产区麦冬和山麦冬原植物的18S~26S r DNA-ITS区碱基序列,结果得到供试的7个不同产区麦冬和山麦冬植株样品rDNA的ITS及5.8S rDNA全序列、18S和26S rDNA部分序列,序列长度在696~711 bp.通过分析比较各ITS序列,表明不同产区麦冬和山麦冬rDNA-ITS区存在差异,可为其分子鉴别提供了依据.
rDNA-ITS of Radix ophiopogonis and Radix liriopes from different regions
The 18S-26S rDNA-ITS base sequences of Radix ophiopogonis and Radix liriopes from different geographical regions were compared by using the specific PCR-ITS. The complete sequences of ITS and 5. 8S rDNA, as well as partial sequences of 18S rDNA and 26S rDNA, in the range of 696-711 bp for the seven samples were obtained. By comparing the sequences, it was apparent that the ITS sequences of R. ophiopogonis and R. liriopes from different regions varied. Our analytical results provided a basis for molecular identification of the species.

Radix ophiopogonisRadix liriopesrDNA-ITS

黄玉吉、陈菁瑛、苏海兰、黄颖桢、万学锋

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福建省农业科学院农业生物资源研究所,福建,福州,350003

福建农林大学园艺植物生物工程研究所,福建,福州,350002

麦冬 山麦冬 rDNA-ITS

国家科技支撑计划福建省农业科学院青年科技人才创新基金

2006BAI06A11-03A2007QJ02

2009

福建农业学报
福建省农业科学院

福建农业学报

CSTPCD
影响因子:0.656
ISSN:1008-0384
年,卷(期):2009.24(6)
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