Dean C, Favreau M, Bedbrook J, Dunsmuir P
Advanced Genetic Sciences, Oakland, California 94608.
Plant Cell. 1989 Feb;1(2):209-15. doi: 10.1105/tpc.1.2.209.
The promoter sequences that contribute to quantitative differences in expression of the petunia genes (rbcS) encoding the small subunit of ribulose bisphosphate carboxylase have been characterized. The promoter regions of the two most abundantly expressed petunia rbcS genes, SSU301 and SSU611, show sequence similarity not present in other rbcS genes. We investigated the significance of these and other sequences by adding specific regions from the SSU301 promoter (the most strongly expressed gene) to equivalent regions in the SSU911 promoter (the least strongly expressed gene) and assaying the expression of the fusions in transgenic tobacco plants. In this way, we characterized an SSU301 promoter region (either from -285 to -178 or -291 to -204) which, when added to SSU911, in either orientation, increased SSU911 expression 25-fold. This increase was equivalent to that caused by addition of the entire SSU301 5'-flanking region. Replacement of SSU911 promoter sequences between -198 and the start codon with sequences from the equivalent region of SSU301 did not increase SSU911 expression significantly. The -291 to -204 SSU301 promoter fragment contributes significantly to quantitative differences in expression between the petunia rbcS genes.
对矮牵牛中编码核酮糖二磷酸羧化酶小亚基的基因(rbcS)表达量产生定量差异的启动子序列进行了表征。矮牵牛中表达量最高的两个rbcS基因SSU301和SSU611的启动子区域,显示出其他rbcS基因中不存在的序列相似性。我们通过将SSU301启动子(表达最强的基因)的特定区域添加到SSU911启动子(表达最弱的基因)的等效区域,并检测转基因烟草植株中融合基因的表达,来研究这些序列及其他序列的意义。通过这种方式,我们鉴定出一个SSU301启动子区域(从-285到-178或从-291到-204),当将其以任何方向添加到SSU911时,可使SSU911的表达增加25倍。这种增加与添加整个SSU301 5'侧翼区域所导致的增加相当。用SSU301等效区域的序列替换SSU911启动子-198与起始密码子之间的序列,并未显著增加SSU911的表达。SSU301启动子-291至-204片段对矮牵牛rbcS基因之间表达量的定量差异有显著贡献。