Plant Biology Laboratory, The Salk Institute for Biological Studies, P. O. Box 85800, San Diego, CA 92138.
Proc Natl Acad Sci U S A. 1984 Sep;81(18):5724-8. doi: 10.1073/pnas.81.18.5724.
DNAs complementary to poly(A)(+) RNA present in elicitor-treated cells of Phaseolus vulgaris L. were inserted into pBR325 and used to transform Escherichia coli strain JA221. A clone was identified that contained sequences complementary to mRNA encoding chalcone synthase, a regulatory enzyme of phenylpropanoid biosynthesis, which catalyzes the first reaction of a branch pathway specific to flavonoid and isoflavonoid biosynthesis. Rapid, marked but transient increases in chalcone synthase mRNA in response to elicitor treatment were observed by RNA blot hybridization with (32)P-labeled chalcone synthase cDNA sequences. Induction of chalcone synthase mRNA governs the rate of enzyme synthesis throughout the phase of rapid increase in enzyme activity at the onset of accumulation of isoflavonoid-derived phytoalexins. The data are consistent with the hypothesis that elicitor causes a rapid transient stimulation of transcription of chalcone synthase gene(s) as an early event in the expression of the phytoalexin defense response.
在长春花细胞的 poly(A)(+) RNA 中,与 DNA 互补的序列被插入 pBR325 中,并用于转化大肠杆菌 JA221 菌株。鉴定出一个含有与 chalcone synthase mRNA 互补序列的克隆,chalcone synthase 是苯丙烷生物合成的调节酶,催化黄酮和异黄酮生物合成的一个分支途径的第一个反应。用 (32)P 标记的 chalcone synthase cDNA 序列进行 RNA 印迹杂交,观察到诱导物处理后 chalcone synthase mRNA 迅速、显著但短暂增加。chalcone synthase mRNA 的诱导控制着酶合成的速率,在异黄酮衍生的植物抗毒素积累开始时,酶活性迅速增加的阶段。这些数据与这样一种假设一致,即诱导物作为植物抗毒素防御反应表达的早期事件,引起 chalcone synthase 基因的快速短暂转录刺激。