Chen X, Wang B, Wu R
Section of Biochemistry, Molecular and Cell Biology, Cornell University, Ithaca, NY 14853, USA.
Plant Mol Biol. 1995 Nov;29(4):787-95. doi: 10.1007/BF00041168.
A ubiquitin-conjugating enzyme (UBC) gene, induced by gibberellin (GA) within an hour, was identified in rice (Oryza sativa) seeds by the mRNA differential display technique. GA inducibility was confirmed by RNA hybridization. A full-length UBC cDNA clone and a genomic clone have been isolated and sequenced. The deduced amino acid sequence shares a significant identity with several known UBC sequences, which are probably involved in the pathway responsible for degrading short-lived regulatory proteins. In vivo transient assays using the UBC gene promoter, joined to the luciferase cDNA as the reporter gene, showed that the sequence located between positions 231 and 159 upstream of the transcription start site of this promoter is crucial for GA-dependent activation of the luciferase cDNA. Finally, trans-activation experiments indicated that this UBC gene is involved in gibberellin-stimulated alpha-amylase gene expression.
通过mRNA差异显示技术,在水稻(Oryza sativa)种子中鉴定出一种在1小时内受赤霉素(GA)诱导的泛素结合酶(UBC)基因。通过RNA杂交证实了GA诱导性。已分离并测序了一个全长UBC cDNA克隆和一个基因组克隆。推导的氨基酸序列与几个已知的UBC序列具有显著的同一性,这些序列可能参与负责降解短命调节蛋白的途径。使用与荧光素酶cDNA连接作为报告基因的UBC基因启动子进行的体内瞬时分析表明,该启动子转录起始位点上游231至159位之间的序列对于GA依赖的荧光素酶cDNA激活至关重要。最后,反式激活实验表明该UBC基因参与赤霉素刺激的α-淀粉酶基因表达。