Silverstone Aron L, Tseng Tong-Seung, Swain Stephen M, Dill Alyssa, Jeong Sun Yong, Olszewski Neil E, Sun Tai-Ping
Department of Biology, Duke University, Durham, North Carolina 27708, USA.
Plant Physiol. 2007 Feb;143(2):987-1000. doi: 10.1104/pp.106.091025. Epub 2006 Dec 1.
The Arabidopsis (Arabidopsis thaliana) SPINDLY (SPY) protein negatively regulates the gibberellin (GA) signaling pathway. SPY is an O-linked N-acetylglucosamine (GlcNAc) transferase (OGT) with a protein-protein interaction domain consisting of 10 tetratricopeptide repeats (TPR). OGTs add a GlcNAc monosaccharide to serine/threonine residues of nuclear and cytosolic proteins. Determination of the molecular defects in 14 new spy alleles reveals that these mutations cluster in three TPRs and the C-terminal catalytic region. Phenotypic characterization of 12 spy alleles indicates that TPRs 6, 8, and 9 and the catalytic domain are crucial for GA-regulated stem elongation, floral induction, and fertility. TPRs 8 and 9 and the catalytic region are also important for modulating trichome morphology and inflorescence phyllotaxy. Consistent with a role for SPY in embryo development, several alleles affect seedling cotyledon number. These results suggest that three of the TPRs and the OGT activity in SPY are required for its function in GA signal transduction. We also examined the effect of spy mutations on another negative regulator of GA signaling, REPRESSOR OF ga1-3 (RGA). The DELLA motif in RGA is essential for GA-induced proteolysis of RGA, and deletion of this motif (as in rga-delta17) causes a GA-insensitive dwarf phenotype. Here, we demonstrate that spy partially suppresses the rga-delta17 phenotype but does not reduce rga-delta17 or RGA protein levels or alter RGA nuclear localization. We propose that SPY may function as a negative regulator of GA response by increasing the activity of RGA, and presumably other DELLA proteins, by GlcNAc modification.
拟南芥(Arabidopsis thaliana)的SPINDLY(SPY)蛋白对赤霉素(GA)信号通路起负调控作用。SPY是一种O-连接的N-乙酰葡糖胺(GlcNAc)转移酶(OGT),具有由10个四肽重复序列(TPR)组成的蛋白质-蛋白质相互作用结构域。OGT会将一个GlcNAc单糖添加到核蛋白和胞质蛋白的丝氨酸/苏氨酸残基上。对14个新的spy等位基因的分子缺陷进行测定发现,这些突变集中在三个TPR和C端催化区域。对12个spy等位基因的表型特征分析表明,TPR6、8和9以及催化结构域对于GA调控的茎伸长、花诱导和育性至关重要。TPR8和9以及催化区域对于调节毛状体形态和花序叶序也很重要。与SPY在胚胎发育中的作用一致,几个等位基因会影响幼苗子叶数量。这些结果表明,SPY中的三个TPR和OGT活性是其在GA信号转导中发挥功能所必需的。我们还研究了spy突变对GA信号的另一个负调控因子——ga1-3抑制子(RGA)的影响。RGA中的DELLA基序对于GA诱导的RGA蛋白水解至关重要,缺失该基序(如在rga-delta17中)会导致GA不敏感的矮化表型。在此,我们证明spy部分抑制rga-delta17表型,但不会降低rga-delta17或RGA蛋白水平,也不会改变RGA的核定位。我们提出,SPY可能通过对RGA以及可能的其他DELLA蛋白进行GlcNAc修饰来增加其活性,从而作为GA反应的负调控因子发挥作用。