Mavandad M, Edwards R, Liang X, Lamb C J, Dixon R A
Plant Biology Division, The Samuel Roberts Noble Foundation, P.O. Box 2180, Ardmore, Oklahoma 73402.
Plant Physiol. 1990 Oct;94(2):671-80. doi: 10.1104/pp.94.2.671.
Using DNA probes specific for the three members of the bean (Phaseolus vulgaris L.) phenylalanine ammonia-lyase (PAL) gene family, we have studied the effects of the product of the PAL reaction, trans-cinnamic acid (CA), on the appearance of individual PAL transcripts in suspension cultured bean cells. Concentrations of CA in excess of 10(-4) molar inhibited appearance of elicitor-induced transcripts encoding PAL1, PAL2, and PAL3 when added to the cells at the same time as fungal elicitor. Addition of CA 4 hours postelicitation caused a major reduction in the levels of all three PAL transcripts, but with different kinetics and subsequent rates of recovery. The inhibition of accumulation of PAL1, PAL2, or PAL3 transcripts, measured 3 hours after exposure to elicitor, as a function of the time of addition of CA postelicitation reflected the different rates of appearance of the three PAL transcripts in the presence of elicitor alone. The inhibitory effects of CA as seen on PAL transcripts were not observed for the constitutively expressed transcript H1, or the elicitor-inducible 1,3-beta-D-glucanase. Analysis of in vitro translated polypeptides showed that some elicitor-induced mRNA activities were not down-regulated by CA, and that a number of other mRNA activities were induced by CA, thus providing further evidence for specificity in the action of CA on bean cells. Treatment of elicited cells with L-alpha-aminooxy-beta-phenylpropionic acid, a potent and specific inhibitor of PAL activity, resulted in maintenance of elevated PAL transcript levels beyond 12 hours postelicitation, this effect being greatest for PAL transcripts 2 and 3. Our results are consistent with a model in which CA, or a derivative, could act as a component in a regulatory feedback system operating at the level of phenylpropanoid gene transcription.
利用针对菜豆(Phaseolus vulgaris L.)苯丙氨酸解氨酶(PAL)基因家族三个成员的DNA探针,我们研究了PAL反应产物反式肉桂酸(CA)对悬浮培养菜豆细胞中单个PAL转录本出现的影响。当与真菌激发子同时添加到细胞中时,超过10^(-4)摩尔浓度的CA抑制了编码PAL1、PAL2和PAL3的激发子诱导转录本的出现。激发后4小时添加CA导致所有三种PAL转录本水平大幅降低,但动力学和随后的恢复速率不同。在暴露于激发子3小时后测量的PAL1、PAL2或PAL3转录本积累的抑制作用,作为激发后添加CA时间的函数,反映了仅在存在激发子的情况下三种PAL转录本出现的不同速率。对于组成型表达的转录本H1或激发子诱导的1,3-β-D-葡聚糖酶,未观察到CA对PAL转录本的抑制作用。对体外翻译多肽的分析表明,一些激发子诱导的mRNA活性未被CA下调,并且一些其他mRNA活性被CA诱导,从而为CA对菜豆细胞作用的特异性提供了进一步证据。用L-α-氨基氧基-β-苯丙酸(一种有效的PAL活性特异性抑制剂)处理激发的细胞,导致PAL转录本水平在激发后12小时以上维持升高,这种效应对于PAL转录本2和3最为明显。我们的结果与一个模型一致,即CA或其衍生物可以作为在苯丙烷类基因转录水平上运行的调节反馈系统的一个组成部分。