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菲油果LEAFY基因的表达模式及启动子克隆
引用本文:冯延芝,张琳,袁德义,龙洪旭,刘敏,张日清,陈圣林.菲油果LEAFY基因的表达模式及启动子克隆[J].植物遗传资源学报,2014,15(4):831-837.
作者姓名:冯延芝  张琳  袁德义  龙洪旭  刘敏  张日清  陈圣林
作者单位:中南林业科技大学,中南林业科技大学,中南林业科技大学,中南林业科技大学,中南林业科技大学,中南林业科技大学,中南林业科技大学
基金项目:国家林业局“948”项目
摘    要:LEAFY(简称LFY)是植物花分生组织特征基因,在植物由营养生长向生殖生长转变过程中起着重要作用,是启动开花的枢纽。菲油果是一种新兴的果树资源,为研究菲油果LFY基因(FsLFY)的表达调控规律,本研究通过实时荧光定量PCR技术研究了FsLFY基因的时空表达模式,并通过染色体步移技术克隆了该基因的启动子序列。荧光定量PCR结果表明,FsLFY基因在菲油果花蕾不同发育阶段以及其他组织器官中均有表达。在花蕾中,小蕾期最高,中蕾期最低;组织器官中,营养枝茎段最高,花瓣最低。FsLFY基因启动子序列长度为2436 bp(GenBank登录号:KF766536),运用PLACE、PlantCARE等在线软件对其序列进行顺式作用元件分析,结果显示该序列不仅含有CAAT-box、TATA-box等核心启动子元件,而且还具有响应水分、光、赤霉素(GA)以及其他功能未知的顺式调控元件,表明FsLFY基因的表达受多种外界环境条件的调控。本研究为阐明菲油果的开花机理,以及通过分子育种手段使菲油果早花早果奠定了理论基础。

关 键 词:菲油果  LFY基因  实时荧光定量PCR  表达模式  启动子
收稿时间:2013/11/29 0:00:00
修稿时间:3/3/2014 12:00:00 AM

The Expression Pattern and its Promoter Cloning of FsLFY Gene in Feijoa Sellowiana
FENG Yan-zhi;ZHANG Lin;YUAN De-yi;LONG Hong-xu;LIU Min;ZHANG Ri-qing;CHEN Sheng-lin.The Expression Pattern and its Promoter Cloning of FsLFY Gene in Feijoa Sellowiana[J].Journal of Plant Genetic Resources,2014,15(4):831-837.
Authors:FENG Yan-zhi;ZHANG Lin;YUAN De-yi;LONG Hong-xu;LIU Min;ZHANG Ri-qing;CHEN Sheng-lin
Institution:FENG Yan-zhi;ZHANG Lin;YUAN De-yi;LONG Hong-xu;LIU Min;ZHANG Ri-qing;CHEN Sheng-lin;Key Laboratory of Cultivation and Protection for Non-Wood Forest Trees,Ministry of Education,Central South University of Forestry and Technology;College of Forestry,Central South University of Forestry and Technology;
Abstract:LFY gene plays an important role in the transformation process from vegetative growth to reproductive growth in flowering plants. Feijoa sellowiana, a promising fruit, was introduced to China recently. To clarify the expression and pattern of the FsLFY (F. sellowiana LFY) gene, the spatial and temporal expression pattern of the FSLFY gene was revealed by real-time fluorescent quantitative PCR (qPCR) technology, and the promoter sequences of the FsLFY gene sequences were isolated by the chromosome walking technology. QPCR analysis showed that the FsLFY gene was expressed at all developmental stages of floral buds and all different tissues/organs. In developmental buds, the expression level of the FsLFY was the highest in small bud stage and the lowest in middle bud stage. In tisses/organs, the expression level was the highest in stems from vegetative branches and the lowest in sepals. The newly cloned FsLFY promoter was 2436 bp in length and was deposited in GenBank under accession no. KF766536. Promoter analysis with online softwares PLACE and PlantCARE showed that the FsLFY promoter contained not only CAAT-box, TATA-box and other core promoter elements, but also the unknown cis-regulatory elements response to the water, light, and gibberellin(GA), implying that the expression of the FsLFY gene is regulated by various external environment conditions. This study would provide atheoretical basis for fully understanding the flowering mechanism of F. sellowiana and accelerating flowering and fruit setting via molecular breeding strategy.
Keywords:Feijoa sellowiana  LFY gene  Real-time fluorescent quantitative PCR  Expression pattern  Promoter
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