Shinwari Z K, Nakashima K, Miura S, Kasuga M, Seki M, Yamaguchi-Shinozaki K, Shinozaki K
Biological Resources Division, Japan International Research Center for Agricultural Sciences (JIRCAS), 1-2, Ohwashi, Ibaraki, Tsukuba, 305-8686, Japan.
Biochem Biophys Res Commun. 1998 Sep 8;250(1):161-70. doi: 10.1006/bbrc.1998.9267.
In higher plants, a cis-acting element, DRE/CRT, is involved in gene expression responsive to drought and low-temperature stress. To understand signal transduction pathways from the cold stress signal to gene expression, we characterized a gene family for DRE/CRT-binding proteins DREB1A and CBF1 in Arabidopsis thaliana. DREB1A and CBF1 were shown to be involved in low-temperature-responsive gene expression. We screened an Arabidopsis genomic DNA library with the cDNA fragment of DREB1A as a probe and isolated DREB1A and 2 related genes, DREB1B (= CBF1) and DREB1C. These were arrayed in the order B, A, C in an 8.7 kb region of Arabidopsis chromosome 4. Northern blot analysis using gene-specific probes showed that the 3 DREB1 genes are induced mainly by cold stress but not by osmotic stress in leaves, roots, and stems. Several conserved sequences were found in the promoter regions of all 3 genes. The beta-glucuronidase (GUS) reporter gene driven by the DREB1 promoters was induced at transcriptional level by low temperature in transgenic Arabidopsis plants.
在高等植物中,一种顺式作用元件DRE/CRT参与了对干旱和低温胁迫的基因表达响应。为了理解从冷胁迫信号到基因表达的信号转导途径,我们对拟南芥中与DRE/CRT结合蛋白DREB1A和CBF1相关的基因家族进行了表征。结果表明,DREB1A和CBF1参与低温响应基因的表达。我们以DREB1A的cDNA片段为探针筛选了拟南芥基因组DNA文库,分离出了DREB1A以及2个相关基因DREB1B(= CBF1)和DREB1C。它们在拟南芥第4号染色体的一个8.7 kb区域内按B、A、C的顺序排列。使用基因特异性探针进行的Northern印迹分析表明,这3个DREB1基因主要在叶片、根和茎中受冷胁迫诱导,而不受渗透胁迫诱导。在这3个基因的启动子区域发现了几个保守序列。在转基因拟南芥植株中,由DREB1启动子驱动的β-葡萄糖醛酸酶(GUS)报告基因在转录水平上受低温诱导。