A soybean (Glycine max) polyubiquitin promoter gives strong constitutive expression in transgenic soybean

被引:71
作者
Hernandez-Garcia, Carlos M. [1 ]
Martinelli, Adriana P. [1 ]
Bouchard, Robert A. [1 ]
Finer, John J. [1 ]
机构
[1] Ohio State Univ, Dept Hort & Crop Sci, OARDC, Wooster, OH 44691 USA
关键词
Promoter characterization; gfp; Gmubi promoter; CaMV35S promoter; Intron; gfp fluorescence; INTRON-MEDIATED ENHANCEMENT; MAIZE UBIQUITIN PROMOTER; RICE RUBI3 GENE; STABLE TRANSFORMATION; 5'-UTR INTRON; PROTEASOME; TISSUE; SEQUENCES; TRANSIENT; PROTEINS;
D O I
10.1007/s00299-009-0681-7
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The success of plant genetic transformation relies greatly on the strength and specificity of the promoters used to drive genes of interest. In this study, we analyzed gfp gene expression mediated by a polyubiquitin promoter (Gmubi) from soybean (Glycine max) in stably transformed soybean tissues. Strong GFP expression was observed in stably transformed proliferative embryogenic tissues. In whole transgenic plants, GFP expression was observed in root tips, main and lateral roots, cotyledons and plumules in young plants as well as in leaf veins, petioles, flower petals, pollen, pods and developing seeds in mature plants. GFP expression was localized mainly in epidermal cells, leaf mesophyll, procambium and vascular tissues. Introduction of an intron-less version of the Gmubi promoter (Gmupri) displayed almost the same GFP expression pattern albeit at lower intensities. The Gmubi promoter showed high levels of constitutive expression and represents an alternative to viral promoters for driving gene expression in soybean.
引用
收藏
页码:837 / 849
页数:13
相关论文
共 55 条
  • [1] [Anonymous], 1989, Molecular Cloning: A Laboratory Manual
  • [2] HISTOCHEMICAL ANALYSIS OF CAMV 35S PROMOTER-BETA-GLUCURONIDASE GENE-EXPRESSION IN TRANSGENIC RICE PLANTS
    BATTRAW, MJ
    HALL, TC
    [J]. PLANT MOLECULAR BIOLOGY, 1990, 15 (04) : 527 - 538
  • [3] ANALYSIS OF A SUNFLOWER POLYUBIQUITIN PROMOTER BY TRANSIENT EXPRESSION
    BINET, MN
    LEPETIT, M
    WEIL, JH
    TESSIER, LH
    [J]. PLANT SCIENCE, 1991, 79 (01) : 87 - 94
  • [4] Comparative analysis of 35S and lectin promoters in transgenic soybean tissue using an automated image acquisition system and image analysis
    Buenrostro-Nava, Marco Tulio
    Ling, Peter P.
    Finer, John J.
    [J]. PLANT CELL REPORTS, 2006, 25 (09) : 920 - 926
  • [5] Approaches to minimize variation of transgene expression in plants
    Butaye, KMJ
    Cammue, BPA
    Delauré, SL
    De Bolle, MFC
    [J]. MOLECULAR BREEDING, 2005, 16 (01) : 79 - 91
  • [6] CALLIS J, 1990, J BIOL CHEM, V265, P12486
  • [7] INTRONS INCREASE GENE-EXPRESSION IN CULTURED MAIZE CELLS
    CALLIS, J
    FROMM, M
    WALBOT, V
    [J]. GENES & DEVELOPMENT, 1987, 1 (10) : 1183 - 1200
  • [8] Ectopic expression of a soybean phytase in developing seeds of Glycine max to improve phosphorus availability
    Chiera, JM
    Finer, JJ
    Grabau, EA
    [J]. PLANT MOLECULAR BIOLOGY, 2004, 56 (06) : 895 - 904
  • [9] Isolation of two highly active soybean (Glycine max (L.) Merr.) promoters and their characterization using a new automated image collection and analysis system
    Chiera, Joseph M.
    Bouchard, Robert A.
    Dorsey, Summer L.
    Park, EuiHo
    Buenrostro-Nava, Marco T.
    Ling, Peter P.
    Finer, John J.
    [J]. PLANT CELL REPORTS, 2007, 26 (09) : 1501 - 1509
  • [10] Ononitol and pinitol production in transgenic soybean containing the inositol methyl transferase gene from Mesembryanthemum crystallinum
    Chiera, Joseph M.
    Streeter, John G.
    Finer, John J.
    [J]. PLANT SCIENCE, 2006, 171 (06) : 647 - 654