Miura Kenji, Rus Ana, Sharkhuu Altanbadralt, Yokoi Shuji, Karthikeyan Athikkattuvalasu S, Raghothama Kashchandra G, Baek Dongwon, Koo Yoon Duck, Jin Jing Bo, Bressan Ray A, Yun Dae-Jin, Hasegawa Paul M
Center for Plant Environmental Stress Physiology, Purdue University, West Lafayette, IN 47907, USA.
Proc Natl Acad Sci U S A. 2005 May 24;102(21):7760-5. doi: 10.1073/pnas.0500778102. Epub 2005 May 13.
Plants sense phosphate (Pi) deficiency and initiate signaling that controls adaptive responses necessary for Pi acquisition. Herein, evidence establishes that AtSIZ1 is a plant small ubiquitin-like modifier (SUMO) E3 ligase and is a focal controller of Pi starvation-dependent responses. T-DNA insertional mutated alleles of AtSIZ1 (At5g60410) cause Arabidopsis to exhibit exaggerated prototypical Pi starvation responses, including cessation of primary root growth, extensive lateral root and root hair development, increase in root/shoot mass ratio, and greater anthocyanin accumulation, even though intracellular Pi levels in siz1 plants were similar to wild type. AtSIZ1 has SUMO E3 ligase activity in vitro, and immunoblot analysis revealed that the protein sumoylation profile is impaired in siz1 plants. AtSIZ1-GFP was localized to nuclear foci. Steadystate transcript abundances of Pi starvation-responsive genes AtPT2, AtPS2, and AtPS3 were moderate but clearly greater in siz1 seedlings than in wild type, where Pi is sufficient. Pi starvation induced the expression of these genes to the same extent in siz1 and wild-type seedlings. However, two other Pi starvation-responsive genes, AtIPS1 and AtRNS1, are induced more slowly in siz1 seedlings by Pi limitation. PHR1, a MYB transcriptional activator of AtIPS1 and AtRNS1, is an AtSIZ1 sumoylation target. These results indicate that AtSIZ1 is a SUMO E3 ligase and that sumoylation is a control mechanism that acts both negatively and positively on different Pi deficiency responses.
植物能感知磷酸盐(Pi)缺乏,并启动信号传导以控制获取Pi所需的适应性反应。在此,有证据表明AtSIZ1是一种植物小泛素样修饰物(SUMO)E3连接酶,是Pi饥饿依赖性反应的关键调控因子。AtSIZ1(At5g60410)的T-DNA插入突变等位基因使拟南芥表现出夸张的典型Pi饥饿反应,包括主根生长停止、侧根和根毛大量发育、根/茎质量比增加以及花青素积累增多,尽管siz1植株的细胞内Pi水平与野生型相似。AtSIZ1在体外具有SUMO E3连接酶活性,免疫印迹分析表明siz1植株中的蛋白质SUMO化谱受损。AtSIZ1-GFP定位于核焦点。Pi饥饿响应基因AtPT2、AtPS2和AtPS3的稳态转录丰度适中,但在Pi充足的siz1幼苗中明显高于野生型。Pi饥饿在siz1和野生型幼苗中诱导这些基因表达的程度相同。然而,另外两个Pi饥饿响应基因AtIPS1和AtRNS1在siz1幼苗中受Pi限制的诱导速度较慢。PHR1是AtIPS1和AtRNS1的MYB转录激活因子,是AtSIZ1的SUMO化靶点。这些结果表明AtSIZ1是一种SUMO E3连接酶,SUMO化是一种对不同Pi缺乏反应起正负调控作用的控制机制。