Dominov J A, Stenzler L, Lee S, Schwarz J J, Leisner S, Howell S H
Boyce Thompson Institute, Ithaca, New York 14853.
Plant Cell. 1992 Apr;4(4):451-61. doi: 10.1105/tpc.4.4.451.
Both cytokinin (N6-benzyladenine [BA]) and auxin (2,4-dichlorophenoxyacetic acid [2,4-D]) stimulate the accumulation of an mRNA, represented by the cDNA pLS216, in Nicotiana plumbaginifolia suspension culture cells. The kinetics of RNA accumulation were different for the two hormones; however, the response to both was transient, and the magnitude of the response was dose dependent. Runoff transcription experiments demonstrated that the transient appearance of the RNA could be accounted for by feedback regulation of transcription and not by the induction of an RNA degradation system. The feedback mechanism appeared to desensitize the cells to further exposure of the hormone. In particular, cells became refractory to the subsequent addition of 2,4-D after the initial RNA accumulation response subsided. A very different response was observed when the second hormone was added to cells that had been desensitized to the first hormone. Under such conditions, BA produced a heightened response in cells desensitized to 2,4-D and vice versa. These findings support a model in which cytokinin further enhances the auxin response or prevents its feedback inhibition. The hormone-induced RNA accumulation was blocked by the protein kinase inhibitor staurosporin. On the other hand, the protein phosphatase inhibitor okadaic acid stimulated expression, and, in particular, okadaic acid was able to stimulate RNA accumulation in cells desensitized to auxin. This suggests that hormone activation involves phosphorylation of critical proteins on the hormone signaling pathway, whereas feedback inhibition may involve dephosphorylation of these proteins. The sequence of pLS216 is similar to genes in other plants that are stimulated by multiple agonists such as auxins, elicitors, and heavy metals, and to the gene encoding the stringent starvation protein in Escherichia coli. It is proposed that this gene family in various plants be called multiple stimulus response (msr) genes.
细胞分裂素(N6-苄基腺嘌呤[BA])和生长素(2,4-二氯苯氧乙酸[2,4-D])均能刺激烟草悬浮培养细胞中一种由cDNA pLS216所代表的mRNA的积累。两种激素诱导RNA积累的动力学不同;然而,对两者的反应都是短暂的,且反应程度呈剂量依赖性。连续转录实验表明,RNA的短暂出现可由转录的反馈调节来解释,而非RNA降解系统的诱导。反馈机制似乎使细胞对激素的进一步暴露不敏感。特别是,在最初的RNA积累反应消退后,细胞对随后添加的2,4-D变得不敏感。当向对第一种激素已不敏感的细胞中添加第二种激素时,观察到一种非常不同的反应。在这种情况下,BA在对2,4-D不敏感的细胞中产生增强的反应,反之亦然。这些发现支持了一种模型,即细胞分裂素进一步增强生长素反应或阻止其反馈抑制。激素诱导的RNA积累被蛋白激酶抑制剂星形孢菌素阻断。另一方面,蛋白磷酸酶抑制剂冈田酸刺激了表达,特别是冈田酸能够在对生长素不敏感的细胞中刺激RNA积累。这表明激素激活涉及激素信号通路中关键蛋白的磷酸化,而反馈抑制可能涉及这些蛋白的去磷酸化。pLS216的序列与其他植物中受生长素、激发子和重金属等多种激动剂刺激的基因以及大肠杆菌中编码严谨饥饿蛋白的基因相似。有人提议将各种植物中的这个基因家族称为多刺激反应(msr)基因。