Sugar-responsible elements in the promoter of a gene for β-amylase of sweet potato

被引:43
|
作者
Maeo, K [1 ]
Tomiya, T [1 ]
Hayashi, K [1 ]
Akaike, M [1 ]
Morikami, A [1 ]
Ishiguro, S [1 ]
Nakamura, K [1 ]
机构
[1] Nagoya Univ, Grad Sch Bioagr Sci, Dept Cellular Mechanisms & Funct, Biochem Lab,Chikusa Ku, Nagoya, Aichi 4648601, Japan
关键词
beta-amylase; cis element; gene expression; sporamin; sugar induction; transgenic tobacco;
D O I
10.1023/A:1010684908364
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Expression of genes coding for sporamin and beta -amylase, the two most abundant proteins in storage roots of sweet potato, is coordinately inducible in atypical vegetative tissues by sugars. A sweet potato gene for beta -amylase (beta -Amy) with introns as well as a beta -Amy::GUS fusion gene composed of the beta -Amy promoter and the GUS coding sequence, both showed sugar-inducible expression in leaves of transgenic tobacco which occurred via a hexokinase-independent pathway. Analyses using various 5'-terminal and internal deletions of the beta -Amy promoter indicated that truncated promoters of beta -Amy containing a sequence between -901 and -820, relative to the transcription start site, and the basic promoter region can confer sugar-inducible expression. This 82 bp region contained the TGGACGG sequence that plays an essential role in the sugar-inducible expression of the truncated promoter of the sporamin gene. Deletion or base substitutions of this element in the truncated beta -Amy promoter abolished the sugar-inducible expression, the results suggesting that the TGGACGG element plays an important role in the coordinate induction of expression of genes for beta -amylase and sporamin by sugars.
引用
收藏
页码:627 / 637
页数:11
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