Tilly J J, Allen D W, Jack T
Department of Biological Sciences, Dartmouth College, Hanover, NH 03755, USA.
Development. 1998 May;125(9):1647-57. doi: 10.1242/dev.125.9.1647.
APETALA3 is a MADS box gene required for normal development of the petals and stamens in the Arabidopsis flower. Studies in yeast, mammals and plants demonstrate that MADS domain transcription factors bind with high affinity to a consensus sequence called the CArG box. The APETALA3 promoter contains three close matches to the consensus CArG box sequence. To gain insights into the APETALA3 regulatory circuitry, we have analyzed the APETALA3 promoter using AP3::uidA(GUS) fusions. 496 base pairs of APETALA3 promoter sequence 5' to the transcriptional start directs GUS activity in the same temporal and spatial expression pattern as the APETALA3 RNA and protein in wild-type flowers. A synthetic promoter consisting of three tandem repeats of a 143 base pair sequence directs reporter gene activity exclusively to petals and stamens in the flower. We have analyzed the role of the CArG boxes by site-specific mutagenesis and find that the three CArG boxes mediate discrete regulatory effects. Mutations in CArG1 result in a decrease in reporter expression suggesting that CArG1 is the binding site for a positively acting factor or factors. Mutations in CArG2 result in a decrease in reporter expression in petals, but the expression pattern in stamens is unchanged. By contrast, mutations in CArG3 result in an increase in the level of reporter gene activity during early floral stages suggesting that CArG3 is the binding site for a negatively acting factor.
APETALA3是一种MADS盒基因,对于拟南芥花中花瓣和雄蕊的正常发育是必需的。在酵母、哺乳动物和植物中的研究表明,MADS结构域转录因子与一个称为CArG盒的共有序列具有高亲和力结合。APETALA3启动子包含三个与共有CArG盒序列紧密匹配的序列。为了深入了解APETALA3调控通路,我们使用AP3::uidA(GUS)融合体分析了APETALA3启动子。转录起始位点上游496个碱基对的APETALA3启动子序列指导GUS活性,其时空表达模式与野生型花中的APETALA3 RNA和蛋白质相同。一个由143个碱基对序列的三个串联重复组成的合成启动子将报告基因活性仅导向花中的花瓣和雄蕊。我们通过位点特异性诱变分析了CArG盒的作用,发现这三个CArG盒介导了不同的调控效应。CArG1中的突变导致报告基因表达下降,表明CArG1是一个正向作用因子或多个正向作用因子的结合位点。CArG2中的突变导致花瓣中报告基因表达下降,但雄蕊中的表达模式不变。相比之下,CArG3中的突变导致花发育早期报告基因活性水平增加,表明CArG3是一个负向作用因子的结合位点。