龙眼LEAFY同源基因启动子的克隆与序列分析  

Cloning and sequence analysis of LEAFY gene promoter from longan(Dimocarpus longan)

作　　者：许家辉[1] 朱娜[2] 温超[2] 曾黎辉[2] 

机构地区：[1]福建省农业科学院果树研究所 [2]福建农林大学园艺学院,福州350002

出　　处：《果树学报》2011年第4期689-693,共5页Journal of Fruit Science

基　　金：国家自然科学基金(30971989)

摘　　要：为了解龙眼LEAFY同源基因(LLFY)的表达调控规律,应用染色体步移方法克隆了809 bp的LLFY启动子序列。用在线软件PlantCARE分析表明,该序列除含有启动子基本元件,如TATA-BOX、CAAT-BOX外,还含有参与生理周期调控、干旱诱导MYB结合位点、ABA响应元件、光响应元件等一些其他的调控序列,推测LLFY的表达受生理周期、干旱、光照等的调控。用FootPrinter在线工具对龙眼等6个物种的LEAFY同源基因启动子进行比较,发现不同植物的启动子具有保守性,也存在差异,表明LEAFY同源基因功能上的分化,LLFY基因具有多种功能。In order to study the expression and regulation rule of LEAFY homolog in longan（LLFY）,a 809 bp fragment of LLFY promoter was cloned by chromosome walking method.Promoter sequence analyzed by PlantCARE and PLACE showed that this promoter fragment had TATA-BOX,CAAT-BOX and some other regulatory elements,such as cis-acting element involved in circadian control,MYB binding site involved in drought-inducibility,cis-acting regulatory element involved in the abscisic acid responsiveness and light responsive element.It was supposed that the expression of LLFY was regulated by circadian,drought,light et al.Compared the promoter of LLFY with other 5 plants by FootPrinter analysis,these promoters had conserved domains while the distribution of transcription factor-binding site had difference.It implied the diversity of gene function of LEAFY genes,and LLFY may had different functions.

关 键 词：龙眼 LEAFY同源基因 启动子 序列分析 

分 类 号：S667.2[农业科学—果树学]