期刊文献+

水稻Os05g0442400基因启动子分析以及由Os05g0442400基因启动子引导GUS报告基因在转基因水稻中的表达

Analysis of the rice Os05g0442400 gene promoter and expression of the GUS fusion gene under control of the rice Os05g0442400 gene promoter in transgenic rice
下载PDF
导出
摘要 采用Plant CARE和PLACE软件分析预测水稻Os05g0442400基因启动子序列中可能存在的顺式作用元件.结果显示,在起始密码子ATG上游1500bp区域内,除了启动子基本的核心作用元件外,还存在一些与植物抵御非生物胁迫过程有关的作用元件、脱落酸应答元件、光诱导启动子作用元件、病原菌诱发因子作用元件,以及根特异性结合位点.采用根癌农杆菌介导法成功将Os05g0442400 promoter::gus构建导入"中花11"水稻.由不同组织部位GUS染液检测表明:在水稻苗期,内源Os05g0442400基因可能主要在根部表达;随着水稻生殖期的延续,水稻内源Os05g0442400基因在颖壳中的表达区域由上向下面积增大,并在抽穗后达到最大表达区域.这些结果可能与Os05g0442400基因启动子上分别存在根特异性结合位点和光诱导启动子作用元件具有一定的联系. The promoter sequence of the rice Os05g0442400 gene was analyzed using Plant CARE and PLACE programs. Except the basic promoter c/s - acting elements, several cis - acting elements, including the elements that related to plant resistance to abiotic stress ,light- inducible promoter elements, pathogen- induced factor elements and the root specific motif, were recognized in a 1500bp promoter sequence upstream of the initial codon ATG. The Os05g0442400 promoter: :gus contruct was transferred in- to rice successfully by Agrobacterium tumefaciens - mediated. The GUS expression in different tissues was assayed using GUS staining. The results showed that endogenous Os05g0442400 gene may mainly expressed in roots. With the continuation of rice re- productive stage, the expression area of Os05g0442400 gene in rice glume increased from top to bottom, and after heading the ex- pression area reached the maximum. These results may have some contact with the root specific motif and light - inducible promot- er elements of Os05g0442400 gene promoter.
出处 《上海师范大学学报(自然科学版)》 2013年第2期186-191,共6页 Journal of Shanghai Normal University(Natural Sciences)
基金 农业部转基因专项项目(2009ZX08009-071B)
关键词 水稻 Os05g0442400基因 启动子 顺式作用元件 转基因 GUS报告基因 rice Os05gO442400 gene promoter cis - acting elements transgenic GUS reporter gene
  • 相关文献

参考文献13

  • 1NANTEL A, QUATRANO R S. Characterization of three rice basic/leucine zipper factors,including two inhibitors of Em- BP - 1 DNA binding activity [ J ]. J Biol Chem, 1996,271 (49) :31296 - 31305.
  • 2RIECHMANN J L, MEYEROWITZ E M. The AP2/EREBP family of plant transcription factors [ J ]. Biol Chem, 1998,379 (6) :633 -646.
  • 3ABE H,YAMAGUCHI SHINOZAKI K, URAO T, et al. Role of Arabidopsis MYC and MYB homologs in drought - and absdfic acid - regulated gene expresfion[ J ]. Plant Cell, 1997,9 ( 10 ) : 1859 - 1868.
  • 4MARTIN C, PAZ -ARES J. MYB transcription factors in plants [ J ]. Trends Genet, 1997,13 (2) :67 -73.
  • 5NADJA B, CLAUS F, SALOME P, et al. A novel DNA binding protein with homology to Myb oncoproteins containing only one repeat can function as a transcriptional activator[ J]. The EMBO Journal, 1994,13 (22) :5383 -5392.
  • 6ANNKATION R, IRIS M, UDO W. The tomato I - box binding factor LeMYBI is a member of a novel class of Myb - like proteins[J]. The Plant Journal,1999,20(6) :641 -652.
  • 7李建粤,吕英海,杨丽君,周永国,李双艳.转反义蜡质基因‘湘晴’及其杂交稻米的直链淀粉含量研究[J].西北植物学报,2008,28(6):1082-1087. 被引量:9
  • 8JEFFERSON R A. , KAVANAGH T A, BEVAN M W. GUS fusions : - glucuronidase as a sensitive and versatile gene fu-sion marker in higher olants [ J]. The EMBO Journal, 1987,6 ( 13 ) : 3901 - 3907.
  • 9陈俊,王宗阳.植物MYB类转录因子研究进展[J].植物生理与分子生物学学报,2002,28(2):81-88. 被引量:74
  • 10LU Huafei,MING Xiaotian,QU Lijia,LIU Meihua,LI Jing,GU Hongya,CHEN Zhangliang.Construction of chimeric inducible promoters by elicitors of rice fungal blast pathogen and their expression in transgenic rice[J].Chinese Science Bulletin,2000,45(3):242-246. 被引量:5

二级参考文献48

共引文献179

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