Miura Kenji, Jin Jing Bo, Lee Jiyoung, Yoo Chan Yul, Stirm Vicki, Miura Tomoko, Ashworth Edward N, Bressan Ray A, Yun Dae-Jin, Hasegawa Paul M
Center for Plant Environmental Stress Physiology, Purdue University, West Lafayette, Indiana 47907-2010, USA.
Plant Cell. 2007 Apr;19(4):1403-14. doi: 10.1105/tpc.106.048397. Epub 2007 Apr 6.
SIZ1 is a SUMO E3 ligase that facilitates conjugation of SUMO to protein substrates. siz1-2 and siz1-3 T-DNA insertion alleles that caused freezing and chilling sensitivities were complemented genetically by expressing SIZ1, indicating that the SIZ1 is a controller of low temperature adaptation in plants. Cold-induced expression of CBF/DREB1, particularly of CBF3/DREB1A, and of the regulon genes was repressed by siz1. siz1 did not affect expression of ICE1, which encodes a MYC transcription factor that is a controller of CBF3/DREB1A. A K393R substitution in ICE1 [ICE1(K393R)] blocked SIZ1-mediated sumoylation in vitro and in protoplasts identifying the K393 residue as the principal site of SUMO conjugation. SIZ1-dependent sumoylation of ICE1 in protoplasts was moderately induced by cold. Sumoylation of recombinant ICE1 reduced polyubiquitination of the protein in vitro. ICE1(K393R) expression in wild-type plants repressed cold-induced CBF3/DREB1A expression and increased freezing sensitivity. Furthermore, expression of ICE1(K393R) induced transcript accumulation of MYB15, which encodes a MYB transcription factor that is a negative regulator of CBF/DREB1. SIZ1-dependent sumoylation of ICE1 may activate and/or stabilize the protein, facilitating expression of CBF3/DREB1A and repression of MYB15, leading to low temperature tolerance.
SIZ1是一种SUMO E3连接酶,可促进SUMO与蛋白质底物的缀合。导致冻害和冷害敏感性的siz1-2和siz1-3 T-DNA插入等位基因通过表达SIZ1在遗传上得到互补,这表明SIZ1是植物低温适应性的调控因子。siz1抑制了冷诱导的CBF/DREB1,特别是CBF3/DREB1A以及调控子基因的表达。siz1不影响ICE1的表达,ICE1编码一种MYC转录因子,是CBF3/DREB1A的调控因子。ICE1中的K393R替代[ICE1(K393R)]在体外和原生质体中阻断了SIZ1介导的SUMO化,确定K393残基为SUMO缀合的主要位点。原生质体中ICE1的SIZ1依赖性SUMO化在低温下受到适度诱导。重组ICE1的SUMO化在体外降低了该蛋白的多聚泛素化。野生型植物中ICE1(K393R)的表达抑制了冷诱导的CBF3/DREB1A表达并增加了冻害敏感性。此外,ICE1(K393R)的表达诱导了MYB15的转录积累,MYB15编码一种MYB转录因子,是CBF/DREB1的负调控因子。ICE1的SIZ1依赖性SUMO化可能激活和/或稳定该蛋白,促进CBF3/DREB1A的表达并抑制MYB15,从而导致低温耐受性。