Cai Bin, Kong Xiangxiong, Zhong Chao, Sun Suli, Zhou Xiao Feng, Jin Yin Hua, Wang Youning, Li Xia, Zhu Zhendong, Jin Jing Bo
Key Laboratory of Plant Molecular Physiology, Institute of Botany, The Chinese Academy of Sciences, Beijing 100093, China.
National Key Facility for Crop Gene Resources and Genetic Improvement, Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing 100081, China.
J Integr Plant Biol. 2017 Jan;59(1):2-14. doi: 10.1111/jipb.12504.
SIZ1 is a small ubiquitin-related modifier (SUMO) E3 ligase that mediates post-translational SUMO modification of target proteins and thereby regulates developmental processes and hormonal and environmental stress responses in Arabidopsis. However, the role of SUMO E3 ligases in crop plants is largely unknown. Here, we identified and characterized two Glycine max (soybean) SUMO E3 ligases, GmSIZ1a and GmSIZ1b. Expression of GmSIZ1a and GmSIZ1b was induced in response to salicylic acid (SA), heat, and dehydration treatment, but not in response to cold, abscisic acid (ABA), and NaCl treatment. Although GmSIZ1a was expressed at higher levels than GmSIZ1b, both genes encoded proteins with SUMO E3 ligase activity in vivo. Heterologous expression of GmSIZ1a or GmSIZ1b rescued the mutant phenotype of Arabidopsis siz1-2, including dwarfism, constitutively activated expression of pathogen-related genes, and ABA-sensitive seed germination. Simultaneous downregulation of GmSIZ1a and GmSIZ1b (GmSIZ1a/b) using RNA interference (RNAi)-mediated gene silencing decreased heat shock-induced SUMO conjugation in soybean. Moreover, GmSIZ1RNAi plants exhibited reduced plant height and leaf size. However, unlike Arabidopsis siz1-2 mutant plants, flowering time and SA levels were not significantly altered in GmSIZ1RNAi plants. Taken together, our results indicate that GmSIZ1a and GmSIZ1b mediate SUMO modification and positively regulate vegetative growth in soybean.
SIZ1是一种小泛素相关修饰物(SUMO)E3连接酶,它介导靶蛋白的翻译后SUMO修饰,从而调节拟南芥的发育过程以及激素和环境胁迫反应。然而,SUMO E3连接酶在作物中的作用在很大程度上尚不清楚。在此,我们鉴定并表征了两种大豆SUMO E3连接酶,即GmSIZ1a和GmSIZ1b。GmSIZ1a和GmSIZ1b的表达在水杨酸(SA)、热和脱水处理下被诱导,但在冷、脱落酸(ABA)和NaCl处理下未被诱导。尽管GmSIZ1a的表达水平高于GmSIZ1b,但这两个基因在体内均编码具有SUMO E3连接酶活性的蛋白质。GmSIZ1a或GmSIZ1b的异源表达挽救了拟南芥siz1 - 2的突变表型,包括矮化、病原体相关基因的组成型激活表达以及ABA敏感的种子萌发。使用RNA干扰(RNAi)介导的基因沉默同时下调GmSIZ1a和GmSIZ1b(GmSIZ1a/b)可降低大豆中热激诱导的SUMO缀合。此外,GmSIZ1RNAi植株的株高和叶片大小减小。然而,与拟南芥siz1 - 2突变植株不同,GmSIZ1RNAi植株的开花时间和SA水平没有显著改变。综上所述,我们的结果表明GmSIZ1a和GmSIZ1b介导SUMO修饰并正向调节大豆的营养生长。