Aleman Lorenzo, Kitamura Jun, Abdel-mageed Haggag, Lee Joohyun, Sun Yan, Nakajima Masatoshi, Ueguchi-Tanaka Miyako, Matsuoka Makoto, Allen Randy D
Department of Plant and Soil Sciences, Texas Tech University, Lubbock, TX 79409, USA.
Plant Mol Biol. 2008 Sep;68(1-2):1-16. doi: 10.1007/s11103-008-9347-z. Epub 2008 May 28.
Gibberellic acid (GA) is both necessary and sufficient to promote fiber elongation in cultured fertilized ovules of the upland cotton variety Coker 312. This is likely due to the temporal and spatial regulation of GA biosynthesis, perception, and subsequent signal transduction that leads to alterations in gene expression and morphology. Our results indicate that the initiation of fiber elongation by the application of GA to cultured ovules corresponds with increased expression of genes that encode xyloglucan endotransglycosylase/hydrolase (XTH) and expansin (EXP) that are involved in promoting cell elongation. To gain a better understanding of the GA signaling components in cotton, that lead to such changes in gene expression, two GA receptor genes (GhGID1a and GhGID1b) and two DELLA protein genes (GhSLR1a and GhSLR1b) that are orthologous to the rice GA receptor (GID1) and the rice DELLA gene (SLR1), respectively, were characterized. Similar to the GA biosynthetic genes, expression of GhGID1a and GhGID1b is under the negative regulation by GA while GA positively regulates GhSLR1a. Recombinant GST-GhGID1s showed GA-binding activity in vitro that was augmented in the presence of GhSLR1a, GhSLR1b, or rice SLR1, indicating complex formation between the receptors and repressor proteins. This was further supported by the GA-dependent interaction of these proteins in yeast cells. Ectopic expression of the GhGID1a in the rice gid1-3 mutant plants rescued the GA-insensitive dwarf phenotype, which demonstrates that it is a functional GA receptor. Furthermore, ectopic expression of GhSLR1b in wild type Arabidopsis led to reduced growth and upregulated expression of DELLA-responsive genes.
赤霉素(GA)对于促进陆地棉品种Coker 312培养的受精胚珠中的纤维伸长既必要又充分。这可能是由于GA生物合成、感知以及随后导致基因表达和形态改变的信号转导的时空调节。我们的结果表明,通过向培养的胚珠施用GA来启动纤维伸长,与编码参与促进细胞伸长的木葡聚糖内转糖基酶/水解酶(XTH)和扩张蛋白(EXP)的基因表达增加相对应。为了更好地了解棉花中导致这种基因表达变化的GA信号成分,对两个GA受体基因(GhGID1a和GhGID1b)和两个DELLA蛋白基因(GhSLR1a和GhSLR1b)进行了表征,它们分别与水稻GA受体(GID1)和水稻DELLA基因(SLR1)直系同源。与GA生物合成基因类似,GhGID1a和GhGID1b的表达受GA负调控,而GA对GhSLR1a起正调控作用。重组GST-GhGID1s在体外显示出GA结合活性,在存在GhSLR1a、GhSLR1b或水稻SLR1的情况下活性增强,表明受体和阻遏蛋白之间形成了复合物。酵母细胞中这些蛋白的GA依赖性相互作用进一步支持了这一点。GhGID1a在水稻gid1-3突变体植物中的异位表达挽救了GA不敏感的矮化表型,这表明它是一种功能性GA受体。此外,GhSLR1b在野生型拟南芥中的异位表达导致生长减少和DELLA反应基因的表达上调。