Biologisches Institut II der Universität, Schänzlestrasse 1, D-7800 Freiburg in Breisgau, Federal Republic of Germany.
Proc Natl Acad Sci U S A. 1984 Feb;81(4):1102-6. doi: 10.1073/pnas.81.4.1102.
The mRNAs encoding two enzymes of phenylpropanoid metabolism, phenylalanine ammonia-lyase (PAL; EC 4.3.1.5) and 4-coumarate:CoA ligase (4CL; EC 6.2.1.12), were induced in cultured parsley cells (Petroselinum hortense) either by irradiation with UV light or by treatment with elicitor, a cell-wall fraction of the fungus Phytophthora megasperma f. sp. glycinea. Two-dimensional gel electrophoresis of the encoded PAL and 4CL proteins revealed that the mRNAs induced by either treatment were very similar if not identical. RNA blot hybridization with cDNAs complementary to these mRNAs was used to measure changes in the mRNA amounts at various times after either treatment. Total cellular PAL and 4CL mRNA amounts increased coordinately after UV irradiation to a maximum at 7 hr and then decreased to uninduced levels by 30 hr with the same kinetics as observed previously for the changes in the translational activities. Treatment with the fungal elicitor also caused coordinated, but more rapid, changes in PAL and 4CL mRNA translational activities, with a sharp peak occurring 3 hr after the addition of elicitor. Corresponding changes in mRNA amounts were observed only for 4CL, whereas the amount of PAL mRNA continued to increase at least up to 20 hr after elicitor addition. Our results suggest that parsley cells respond to UV irradiation or addition of fungal elicitor by increased rates of transcription of genes involved in the synthesis of compounds related to UV or disease resistance, respectively.
苯丙烷代谢的两种酶,苯丙氨酸解氨酶(PAL;EC 4.3.1.5)和 4-香豆酸:CoA 连接酶(4CL;EC 6.2.1.12)的 mRNA 在经紫外线照射或用真菌 Phytophthora megasperma f. sp. glycinea 细胞壁部分处理的培养欧芹细胞(Petroselinum hortense)中被诱导。用编码 PAL 和 4CL 蛋白的 cDNA 进行 RNA 印迹杂交,以测量两种处理后不同时间的 mRNA 量变化。用与这些 mRNA 互补的 cDNA 进行 RNA 印迹杂交,以测量两种处理后不同时间的 mRNA 量变化。用与这些 mRNA 互补的 cDNA 进行 RNA 印迹杂交,以测量两种处理后不同时间的 mRNA 量变化。经紫外线照射后,总细胞 PAL 和 4CL mRNA 量协同增加,7 小时达到最大值,然后在 30 小时降至未诱导水平,与先前观察到的翻译活性变化的动力学相同。真菌激发子的处理也导致 PAL 和 4CL mRNA 翻译活性的协同但更快的变化,在添加激发子时出现 3 小时的急剧峰值。仅观察到 4CL 的 mRNA 量发生相应变化,而 PAL mRNA 的量至少在添加激发子后 20 小时内继续增加。我们的结果表明,欧芹细胞分别通过增加与紫外线或疾病抗性相关化合物合成相关基因的转录率来响应紫外线照射或添加真菌激发子。