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毛白杨PtSEP2基因启动子克隆和瞬时表达特性分析
引用本文:崔东清,叶梅霞,刘军梅,李昊,张志毅,安新民.毛白杨PtSEP2基因启动子克隆和瞬时表达特性分析[J].中国生物工程杂志,2011,31(5):42-47.
作者姓名:崔东清  叶梅霞  刘军梅  李昊  张志毅  安新民
作者单位:北京林业大学林木育种国家工程实验室 林木花卉遗传育种教育部重点实验室 国家林业局树木花卉育种与生物工程重点开放实验室 北京 100083
基金项目:国家自然科学基金,国家林业公益性项目,教育部重点项目
摘    要:利用PCR技术从毛白杨基因组DNA中扩增获得花器官发育相关的SEPALLATA2类似基因PtSEP25′侧翼约2.3kb的一段序列,经PlantCARE序列分析表明,该序列中含有启动子特征的保守序列及多种光应答元件,初步推测其为PtSEP2基因启动子.进一步以GUS为报告基因,构建了pPtSEP2 promoter::...

关 键 词:毛白杨  SEPALLATA2  启动子  GUS活性  瞬时表达
收稿时间:2010-11-24
修稿时间:2011-02-11

Cloning and Transient Expression Analysis of PtSEP2 Promoter from Populus tomentosa
CUI Dong-qing,YE Mei-xia,LIU Jun-mei,LI Hao,ZHANG Zhi-yi,AN Xin-min.Cloning and Transient Expression Analysis of PtSEP2 Promoter from Populus tomentosa[J].China Biotechnology,2011,31(5):42-47.
Authors:CUI Dong-qing  YE Mei-xia  LIU Jun-mei  LI Hao  ZHANG Zhi-yi  AN Xin-min
Institution:CUI Dong-qing YE Mei-xia LIU Jun-mei LI Hao ZHANG Zhi-yi AN Xin-min(National Engineering Laboratory for Tree Breeding,Key Laboratory of Genetics and Breeding in Forest Trees and Ornamental Plants,Ministry of Education,The Tree and Ornamental Plant Breeding and Biotechnology Laboratory of State Forestry Administration,Beijing Forestry University,Beijing 100083,China)
Abstract:A 5' flanking sequence of PtSEP2 which is a SEPALLATA2 -like gene involved in floral organ development was amplified by PCR from the genomic DNA of Populus tomentosa. The length of fragment is approximately 2.3kb. The results derived from PlantCARE analysis showed that the sequence contains conserved cis-acting elements of promoter, coupled with a variety of light-responsive elements. Therefore, it was speculated preliminarily to be the promoter of PtSEP2 gene. To investigate function of this promoter, it was fused to GUS reporter gene, generating a plant expression vector pPtSEP2 promoter∷GUS, named PtSEP2p∷GUS . With roots, stems, leaves and flower buds of Nicotiana tobaccum for the receptor, the results of transient expression that Agrobacterium-mediated that showed the PtSEP2 promoter was competent to drive specially GUS reporter gene expression in anther, yet its’ activity was weaker than that of cauliflower mosaic virus (CaMV) 35S promoter, which constitutively expressed in planta. Consequently, provides a possible genetic modification tool for flowering regulation in poplar and other plants.
Keywords:Populus tomentosa SEPALLATA2 promoter GUS activity Transient expression  
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