CIS-ACTING DNA ELEMENTS RESPONSIVE TO GIBBERELLIN AND ITS ANTAGONIST ABSCISIC-ACID

被引:272
作者
SKRIVER, K
OLSEN, FL
ROGERS, JC
MUNDY, J
机构
[1] CARLSBERG LAB, CARLSBERG RES LAB, GL CARLSBERG VEJ 10, DK-2500 COPENHAGEN, DENMARK
[2] CARLSBERG LAB, DEPT PHYSIOL, DK-2500 COPENHAGEN, DENMARK
[3] WASHINGTON UNIV, SCH MED, DIV HEMATOL & ONCOL, ST LOUIS, MO 63110 USA
关键词
ALEURONE PROTOPLAST; GENE EXPRESSION; HORMONE RESPONSE ELEMENT; INDUCIBLE ENHANCER;
D O I
10.1073/pnas.88.16.7266
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We have used a transient expression assay in aleurone protoplasts of barley to delineate hormone response elements of the abscisic acid (ABA)-responsive rice gene Rab-16A and of the gibberellin A3 (GA3)-responsive barley alpha-amylase gene Amy 1/6-4. Our approach used transcriptional fusions between their 5' upstream sequences and a bacterial chloramphenicol acetyltransferase reporter gene. A chimeric promoter containing six copies of the -181 to -171 region of Rab 16A fused to a minimal promoter conferred ABA-responsive expression on the reporter gene. Transcription from this ABA response element (GTACGTGGCGC) was unaffected by GA3. A chimeric promoter containing six copies of the -148 to -128 sequence of Amy 1/6-4 fused to the minimal promoter conferred GA3-responsive expression on the reporter gene. Transcription from this GA3 response element (GGCCGATAACAAACTCCGGCC) was repressed by ABA. The effect on transcription from both hormone response elements was orientation-independent, indicating that they function as inducible enhancers in their native genes.
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页码:7266 / 7270
页数:5
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