期刊文献+

空间飞行水稻pi-hit-1基因启动子功能分析 被引量:2

Function analysis of space flight rice pi-hit-1 gene promoter
下载PDF
导出
摘要 pi-hit-1基因是本实验室通过空间诱变找到的一个水稻新基因。为了对pi-hit-1基因启动子结构和功能进行研究,首先使用植物启动子分析数据库(PlantProm DB-TSSP,TFSEARCH,PLACE及PlantCARE)对该基因转录调控区序列进行预测分析,结果显示该基因上游调控区存在多个顺式元件,主要集中在翻译起始位点前300bp的区域,转录起始位点位于翻译起始位点前100bp,在转录起始位点前132bp存在TATA box元件。凝胶电泳迁移率实验(EMSA)发现翻译起始位点上游约300bp存在转录因子特异结合位点,为该基因的核心启动子,这与预测结果一致。采用系统生物学的方法研究水稻新基因pi-hit-1启动子结构,发现了该基因的核心启动子元件,为研究空间环境如何影响基因的转录调控提供了重要依据。 pi-hit-1 gene was a novel gene identified from space flight rice,and was predicted as a blast related gene.To analyze the structure and function of pi-hit-1 promoter,the gene promoter analyze softwares(PlantProm DB-TSSP,TFSEARCH,PLACE PlantCARE)were used to predict the promoter of pi-hit-1 gene.Result showed there are some cis-elements in about 300bp upstream of pi-hit-1 gene.The transcription start site is at 100 bp upstream of the translation start site.There is a TATA box in 132bp upstream of the transcription stare site.EMSA was used to analyze the promoter.The result showed that the sequence of the sample was same to the predict sequence about the TATA box.
出处 《生物学杂志》 CAS CSCD 2011年第2期1-4,24,共5页 Journal of Biology
基金 国家自然科学基金资助项目(30670176)
关键词 空间飞行 基因 水稻 pi-hit-1基因 启动子 凝胶电泳迁移率实验 space flight genes rice pi-hit-1 gene promoter EMSA
  • 相关文献

参考文献16

  • 1李常银,杨谦,王晓飞,孙野青.抗稻瘟病新基因pi-hit-1的克隆与功能研究[J].高技术通讯,2004,14(10):21-26. 被引量:5
  • 2Romer P,Recht S,Lahaye T.A single plant resistance gene promoter engineered to recognize multiple TAL effeetors from disparate pathogens[J].PANS.2009,106(48):20526-20531. 被引量:1
  • 3Kovalchuk N.Li M,Wittek F,et al.Defensin promoters as potential tools for engineering disease resistance in cereal grains[J].Plant Biotechnol Journal,2009,1(8):47-64. 被引量:1
  • 4Yamaji N,Huang C F,Nngao S,et al.A zinc finger transcription factor ART1 regulates multiple genes implicated in aluminum tolerance in rice[J].plant Cell,2009,21(10):3339-3349. 被引量:1
  • 5Higa K,Ugawa Y,Iwamoto M,et al.Plant cis-acting regulatory DNA elements (PLACE) database:1999[J].Nucleic Acids Res,1999,27(1):297-300. 被引量:1
  • 6Lescot M,De hais P,Thijs G,et al.PlantCARE,a database of plant cisacting regulatory elements and a portal to tools for in silico analysis of promoter sequences[J].Nucleic Acids Res,2002,30(1):325-327. 被引量:1
  • 7王海华,谢科,吴坤陆,郭泽建.稻瘟菌诱导的水稻WRKY基因OsWRKY52的分离和鉴定(英文)[J].生物化学与生物物理进展,2005,32(10):937-946. 被引量:14
  • 8Jung H W,Kim K D.Hwang B K.Identification of pathogen-responsive regions in the promoter of a pepper lipid transfer protein gene (CALTPI) and the enhanced resistance of the CALTPI transgenic Arabidopsis against pathogen and environmental stresses[J].Plants,2005,221(3):361-373. 被引量:1
  • 9Xiang Y,Tang N,De H,et al.Characterization of OsbZIP23 as a key player of the basic leucine zipper transcription factor family for conferring abscisic acid sensitivity and salinity and drought tolerance in rice[J].Plant Phyziol,2008,148(4):1938-1952. 被引量:1
  • 10Guo J J,Wang J B,Xi L,et al.RACKI is a negative regulator of ABA responses in Arabidopsis[J].Journal of Experimental Botany,2009,60(13):3819-3833. 被引量:1

二级参考文献6

共引文献17

同被引文献56

引证文献2

二级引证文献18

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部