Abe Hiroshi, Urao Takeshi, Ito Takuya, Seki Motoaki, Shinozaki Kazuo, Yamaguchi-Shinozaki Kazuko
Biological Resources Division, Japan International Research Center for Agricultural Sciences, 1-1 Ohwashi, Tsukuba, Ibaraki 305-8686, Japan.
Plant Cell. 2003 Jan;15(1):63-78. doi: 10.1105/tpc.006130.
In Arabidopsis, the induction of a dehydration-responsive gene, rd22, is mediated by abscisic acid (ABA). We reported previously that MYC and MYB recognition sites in the rd22 promoter region function as cis-acting elements in the drought- and ABA-induced gene expression of rd22. bHLH- and MYB-related transcription factors, rd22BP1 (renamed AtMYC2) and AtMYB2, interact specifically with the MYC and MYB recognition sites, respectively, in vitro and activate the transcription of the beta-glucuronidase reporter gene driven by the MYC and MYB recognition sites in Arabidopsis leaf protoplasts. Here, we show that transgenic plants overexpressing AtMYC2 and/or AtMYB2 cDNAs have higher sensitivity to ABA. The ABA-induced gene expression of rd22 and AtADH1 was enhanced in these transgenic plants. Microarray analysis of the transgenic plants overexpressing both AtMYC2 and AtMYB2 cDNAs revealed that several ABA-inducible genes also are upregulated in the transgenic plants. By contrast, a Ds insertion mutant of the AtMYC2 gene was less sensitive to ABA and showed significantly decreased ABA-induced gene expression of rd22 and AtADH1. These results indicate that both AtMYC2 and AtMYB2 proteins function as transcriptional activators in ABA-inducible gene expression under drought stress in plants.
在拟南芥中,脱水应答基因rd22的诱导由脱落酸(ABA)介导。我们之前报道过,rd22启动子区域中的MYC和MYB识别位点在rd22的干旱和ABA诱导的基因表达中作为顺式作用元件发挥作用。bHLH和MYB相关转录因子rd22BP1(重新命名为AtMYC2)和AtMYB2分别在体外与MYC和MYB识别位点特异性相互作用,并激活拟南芥叶原生质体中由MYC和MYB识别位点驱动的β-葡萄糖醛酸酶报告基因的转录。在此,我们表明过表达AtMYC2和/或AtMYB2 cDNA的转基因植物对ABA具有更高的敏感性。在这些转基因植物中,ABA诱导的rd22和AtADH1基因表达增强。对过表达AtMYC2和AtMYB2 cDNA的转基因植物进行微阵列分析表明,一些ABA诱导基因在转基因植物中也上调。相比之下,AtMYC2基因的Ds插入突变体对ABA不太敏感,并且显示出ABA诱导的rd22和AtADH1基因表达显著降低。这些结果表明,在植物干旱胁迫下,AtMYC2和AtMYB2蛋白在ABA诱导的基因表达中均作为转录激活因子发挥作用。