Küster H, Quandt H J, Broer I, Perlick A M, Pühler A
Universität Bielefeld, Lehrstuhl für Genetik, Bielefeld, Germany.
Plant Mol Biol. 1995 Nov;29(4):759-72. doi: 10.1007/BF00041166.
We recently reported on the broad bean gene VfENOD-GRP3 encoding a glycine-rich early nodulin. This gene was predominantly expressed in the interzone II-III region of Vicia faba root nodules. The VfENOD-GRP3 promoter contained several sequence motifs potentially involved in the regulation of gene expression. To investigate the molecular basis for the specific VfENOD-GRP3 expression, defined VfENOD-GRP3 promoter fragments were fused to an intron-containing gusAint gene. Agrobacterium rhizogenes ARqual strains carrying these fusions integrated into the TL DNA were used to generate hairy roots on Vicia hirsuta, which subsequently were nodulated. Histochemical analysis of transgenic nodules indicated that a strong gusAint expression in the interzone II-III region was mediated by the -1252/+10 VfENOD-GRP3 promoter region. This reporter gene expression in V. hirsuta was comparable to the location of VfENOD-GRP3 transcripts in V. faba nodules. An analysis of defined promoter fragments revealed that a strong gusAint expression in the interzone II-III region was also mediated by the -737/+10 promoter, whereas the -239/+10 promoter only mediated a weak gusAint expression in the interzone II-III region. Since the -239/+10 promoter fragment did not resemble published nodulin gene promoters, we propose that it contains new sequence motifs involved in mediating gene expression in the interzone II-III region of Vicia nodules.
我们最近报道了蚕豆基因VfENOD - GRP3,它编码一种富含甘氨酸的早期结瘤素。该基因主要在蚕豆根瘤的II - III区表达。VfENOD - GRP3启动子包含几个可能参与基因表达调控的序列基序。为了研究VfENOD - GRP3特异性表达的分子基础,将特定的VfENOD - GRP3启动子片段与含内含子的gusAint基因融合。携带这些融合体并整合到TL DNA中的发根农杆菌ARqual菌株用于在硬毛野豌豆上产生毛状根,这些毛状根随后形成根瘤。对转基因根瘤的组织化学分析表明,- 1252 / + 10 VfENOD - GRP3启动子区域介导了II - III区强烈的gusAint表达。在硬毛野豌豆中的这种报告基因表达与蚕豆根瘤中VfENOD - GRP3转录本的位置相当。对特定启动子片段的分析表明,- 737 / + 10启动子也介导了II - III区强烈的gusAint表达,而- 239 / + 10启动子仅介导了II - III区较弱的gusAint表达。由于- 239 / + 10启动子片段与已发表的结瘤素基因启动子不同,我们推测它包含参与介导蚕豆根瘤II - III区基因表达的新序列基序。