Max-Planck-Institut für Züchtungsforschung, D-5000 Köln 30, FRG.
EMBO J. 1987 May;6(5):1189-95. doi: 10.1002/j.1460-2075.1987.tb02353.x.
We have isolated genomic clones encoding 4-coumarate:CoA ligase (4CL), a key enzyme of general phenylpropanoid metabolism, and have analysed the structure and regulation of the genes contained on these clones. Restriction enzyme and sequence analysis indicated that two distinct 4CL genes, Pc4CL-1 and Pc4CL-2, are represented on the clones and that additional 4CL genes are not present in parsley. Two lines of evidence suggest that each gene is transcriptionally activated by both elicitor and u.v. irradiation: cDNA clones corresponding to each gene were found in cDNA libraries made with RNA from both elicitor-treated and u.v-irradiated cells, and run-off transcripts homologous to a Pc4CL-2-specific intron probe were induced by both treatments. This induction was about half of the induction measured using probes homologous to both genes. The transcription initiation sites of both genes were determined. Comparison of the nucleotide sequences of the two genes 5' to these sites showed that they are highly homologous for several hundred base pairs and that they contain features potentially involved in regulation by elicitor and u.v. irradiation.
我们已经分离出编码 4-香豆酸:辅酶 A 连接酶(4CL)的基因组克隆,4CL 是一般苯丙烷代谢的关键酶,并分析了这些克隆中包含的基因的结构和调控。限制酶和序列分析表明,在克隆中存在两个不同的 4CL 基因 Pc4CL-1 和 Pc4CL-2,而在欧芹中不存在其他 4CL 基因。有两条证据表明,每个基因都被诱导剂和 u.v. 辐射转录激活:从用来自诱导剂处理和 u.v. 辐射的细胞的 RNA 制成的 cDNA 文库中发现了与每个基因相对应的 cDNA 克隆,并且与 Pc4CL-2 特异性内含子探针同源的转录本在两种处理下均被诱导。这种诱导大约是使用与两个基因都同源的探针测量的诱导的一半。两个基因的转录起始位点都被确定。比较这些位点 5' 处两个基因的核苷酸序列表明,它们在几百个碱基对内高度同源,并且它们包含可能涉及诱导剂和 u.v. 辐射调控的特征。