Isolation of the promoter of a cotton β-galactosidase gene (GhGal1) and its expression in transgenic tobacco plants

被引:10
作者
Wu Aimin
Liu Jinyuan [1 ]
机构
[1] Tsinghua Univ, Mol Biol Lab, Minist Educ, Dept Biol Sci & Biotechnol, Beijing 100084, Peoples R China
[2] Tsinghua Univ, Prot Sci Lab, Minist Educ, Dept Biol Sci & Biotechnol, Beijing 100084, Peoples R China
来源
SCIENCE IN CHINA SERIES C-LIFE SCIENCES | 2006年 / 49卷 / 02期
关键词
cotton; beta-galactosidase; transgenic tobacco; promoter activity; fruit and trichome expression;
D O I
10.1007/s11427-006-0105-7
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
beta-galactosidases (EC 3.2.1.23) constitute a widespread family of glycosyl hydrolases in plants and are thought to be involved in metabolism of cell wall polysaccharides. A cDNA of the cotton (Gossypium hirsutum) beta-galactosidase gene, designated GhGal1, has previously been identified and its transcripts are highly abundant at the elongation stage of the cotton fiber. To examine the temporal and spatial control of GhGal1 expression, a transcriptional fusion of the GhGal1 promoter region (1770 bp) with the beta-glucuronidase (GUS) reporter gene was introduced into tobacco plants by the Agrobacterium infection method. The resulting transgenic plants showed higher GUS activity of fruit in the transgenic plants than that in the negative and positive controls. Histochemical localization of GUS activity demonstrated that the expression of the GUS gene could be found in the meristem zones of roots, cotyledons, vascular tissues, fruit and trichomes in transgenic tobacco plants. Additionally, sequence analysis of the regulatory region also revealed several conserved motifs among which some were shared with previously reported fruit/seed-specific elements and the others were related with trichome expression. These results indicated the temporal and spatial expression characterization of the GhGal1 promoter in transgenic tobacco plants and provided an important insight into the roles of GhGal1 in cotton fiber development.
引用
收藏
页码:105 / 114
页数:10
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