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烟草黄酮醇合成酶基因的克隆及其序列分析
引用本文:黄伟伟,杨曦,张常娥,方斌,马靓,常俊丽,杨广笑,何光源. 烟草黄酮醇合成酶基因的克隆及其序列分析[J]. 植物生理学通讯, 2006, 42(6): 1059-1062
作者姓名:黄伟伟  杨曦  张常娥  方斌  马靓  常俊丽  杨广笑  何光源
作者单位:华中科技大学中英HUST-RRes基因工程和基因组学联合实验室,武汉,430074
基金项目:国家重点基础研究发展计划(973计划);国家自然科学基金
摘    要:根据已知的黄酮醇合成酶cDNA保守序列设计引物,用RT-PCR技术从烟草叶片中扩增获得黄酮醇合成酶cDNA片段,再用RACE方法得到其两端序列。根据获得的序列,设计引物分离得到完整的1188bp的黄酮醇合成酶基因,其开放阅读框编码346个氨基酸。序列分析显示,烟草黄酮醇合成酶与高杯花、矮牵牛和马铃薯的同源性分别为87%、86%和84%,与其它物种中的同源性也在80%左右,表明不同物种中黄酮醇合成酶基因具有高度同源性。此外,在氨基酸水平上,该酶与其它依赖于2-酮戊二酸的双加氧酶及其相关酶也具有同源性。

关 键 词:烟草  黄酮醇合成酶基因  序列分析
收稿时间:2006-07-11
修稿时间:2006-11-16

Cloning and Sequence Analysis of Flavonol Synthase Gene from Tobacco (Nicotiana tabacun L.)
HUANG Wei-Wei,YANG Xi,ZHANG Chang-E,FANG Bin,MA Liang,CHANG Jun-Li,YANG Guang-Xiao,HE Guang-Yuan. Cloning and Sequence Analysis of Flavonol Synthase Gene from Tobacco (Nicotiana tabacun L.)[J]. Plant Physiology Communications, 2006, 42(6): 1059-1062
Authors:HUANG Wei-Wei  YANG Xi  ZHANG Chang-E  FANG Bin  MA Liang  CHANG Jun-Li  YANG Guang-Xiao  HE Guang-Yuan
Affiliation:China-UK HUST-RRes Genetic Engineering and Genomics Joint Laboratory, Huazhong University of Science and Technology, Wuhan 430074, China
Abstract:According to the conserved cDNA sequence of flavonol synthase(FLS)gene,a pair of primers was designed,and FLS was cloned from tobacco(Nicotiana tabacun L.)leaves using RT-PCR and RACE.The full length cDNA sequence was 1 188 bp and it included a open reading frame(ORF)which encoded 346 residues.Sequence analysis showed that homologies of FLS cDNA from tobacco with Nierembergia caernlea,Petunia hybrida and Solanum tuberosum were 87%,86% and 84%,and which among the others were about 80%.The results indicated that FLS was highly stable in evolution of plants.On the other hand,it also had similarity with other 2-oxoglutarate-dependent dioxygenases on amino acids level.
Keywords:RACE
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