Lee Heyoung, Cha Jooyoung, Choi Changhyun, Choi Naeyoung, Ji Hyun-So, Park Sang Ryeol, Lee Seungbum, Hwang Duk-Ju
National Institute of Agricultural Sciences, Jeonju, 54874, Republic of Korea.
Rice (N Y). 2018 Jan 12;11(1):5. doi: 10.1186/s12284-018-0199-0.
Plants are frequently subjected to abiotic and biotic stresses, and WRKY proteins play a pivotal role in the response to such stress. OsWRKY11 is induced by pathogens, drought, and heat, suggesting a function in biotic and abiotic stress responses.
This study identified OsWRKY11, a member of WRKY group IIc. It is a transcriptional activator that localized to the nucleus. Ectopic expression of OsWRKY11 resulted in enhanced resistance to a bacterial pathogen, Xanthomonas oryzae pv. oryzae; resistance was compromised in transgenic lines under-expressing OsWRKY11. Ectopic expression of OsWRKY11 resulted in constitutive expression of defense-associated genes, whereas knock-down (kd) of OsWRKY11 reduced expression of defense-associated genes during pathogen attack, suggesting that OsWRKY11 activates defense responses. OsWRKY11 bound directly to the promoter of CHITINASE 2, a gene associated with defense, and activated its transcription. In addition, ectopic expression of OsWRKY11 enhanced tolerance to drought stress and induced constitutive expression of drought-responsive genes. Induction of drought-responsive genes was compromised in OsWRKY11-kd plants. OsWRKY11 also bound directly to the promoter of a drought-responsive gene, RAB21, activating its transcription. In addition, OsWRKY11 protein levels were controlled by the ubiquitin-proteasome system.
OsWRKY11 integrates plant responses to pathogens and abiotic stresses by positively modulating the expression of biotic and abiotic stress-related genes.
植物经常遭受非生物和生物胁迫,WRKY蛋白在应对此类胁迫中起关键作用。OsWRKY11受病原体、干旱和高温诱导,表明其在生物和非生物胁迫反应中发挥作用。
本研究鉴定了WRKY IIc组的成员OsWRKY11。它是一种定位于细胞核的转录激活因子。OsWRKY11的异位表达导致对水稻白叶枯病菌(Xanthomonas oryzae pv. oryzae)的抗性增强;在OsWRKY11表达不足的转基因系中,抗性受损。OsWRKY11的异位表达导致防御相关基因的组成型表达,而敲低(kd)OsWRKY11会降低病原体攻击期间防御相关基因的表达,这表明OsWRKY11激活防御反应。OsWRKY11直接与防御相关基因几丁质酶2(CHITINASE 2)的启动子结合,并激活其转录。此外,OsWRKY11的异位表达增强了对干旱胁迫的耐受性,并诱导了干旱响应基因的组成型表达。在OsWRKY11-kd植物中,干旱响应基因的诱导受到损害。OsWRKY11还直接与干旱响应基因RAB21的启动子结合,激活其转录。此外,OsWRKY11蛋白水平受泛素-蛋白酶体系统调控。
OsWRKY11通过正向调节生物和非生物胁迫相关基因的表达,整合植物对病原体和非生物胁迫的反应。