Horvath D M, Huang D J, Chua N H
Laboratory of Plant Molecular Biology, Rockefeller University, New York, NY 10021 USA.
Mol Plant Microbe Interact. 1998 Sep;11(9):895-905. doi: 10.1094/MPMI.1998.11.9.895.
We have identified and characterized fragments of 15 salicylic acid (SA) early response genes. The kinetics of induction and response to cycloheximide (CHX) treatment allowed classification of genes into four groups. Classes I-III are characterized by immediate-early responses, showing increased accumulation of mRNA within 30 min of SA treatment. Moreover, CHX did not block induction of these genes, indicating that latent cellular factors mediate the SA response. Class IV genes were induced more slowly, but still within 2 to 3 h of SA treatment, and required protein synthesis for expression. Although identified in this study as SA-responsive genes, several could also be induced by other compounds. Two genes were characterized in more detail, including isolation of cDNA sequences and additional analysis of gene expression. Sequence analysis revealed that the class I gene, C18-1, is the previously identified ethylene response element binding protein 1 (EREBP1), an ethylene-induced transcription factor for basic pathogenesis-related (PR) genes, whereas the class III gene, G8-1, is a novel sequence. G8-1 was found to be strongly induced only by SA and its active analogs and was exquisitely sensitive to low SA concentrations. These and other genes were found to be activated at early times following tobacco mosaic virus infection of resistant tobacco genotypes.
我们已经鉴定并描述了15个水杨酸(SA)早期反应基因的片段。通过诱导动力学以及对环己酰亚胺(CHX)处理的反应,可将这些基因分为四类。I - III类基因的特征是早期快速反应,在SA处理后30分钟内mRNA积累增加。此外,CHX并未阻断这些基因的诱导,这表明潜在的细胞因子介导了SA反应。IV类基因诱导较慢,但仍在SA处理后2至3小时内诱导,且其表达需要蛋白质合成。尽管在本研究中被鉴定为SA反应基因,但其中几个基因也可被其他化合物诱导。对两个基因进行了更详细的表征,包括cDNA序列的分离以及基因表达的进一步分析。序列分析表明,I类基因C18 - 1是先前鉴定的乙烯反应元件结合蛋白1(EREBP1),一种乙烯诱导的基础病程相关(PR)基因的转录因子,而III类基因G8 - 1是一个新序列。发现G8 - 1仅被SA及其活性类似物强烈诱导,并且对低SA浓度极为敏感。在抗性烟草基因型被烟草花叶病毒感染后的早期,发现这些基因以及其他基因被激活。