Peng Xixu, Wang Haihua, Jang Jyan-Chyun, Xiao Ting, He Huanhuan, Jiang Dan, Tang Xinke
School of Life Science, Hunan University of Science and Technology, Taoyuan Rd., Xiangtan, Hunan, 411201, China.
Key Laboratory of Ecological Remediation and Safe Utilization of Heavy Metal-polluted Soils, College of Hunan Province, Xiangtan, Hunan, 411201, China.
Rice (N Y). 2016 Dec;9(1):63. doi: 10.1186/s12284-016-0137-y. Epub 2016 Nov 25.
Plant WRKY transcription factors play pivotal roles in diverse biological processes but most notably in plant defense response to pathogens. Sheath blight represents one of the predominant diseases in rice. However, our knowledge about the functions of WRKY proteins in rice defense against sheath blight is rather limited.
Here we demonstrate that the expression of Oryza sativa WRKY80 gene (OsWRKY80) is rapidly and strongly induced upon infection of Rhizoctonia solani, the causal agent of rice sheath blight disease. OsWRKY80 expression is also induced by exogenous jasmonic acid (JA) and ethylene (ET), but not by salicylic acid (SA). OsWRKY80-GFP is localized in the nuclei of onion epidermal cells in a transient expression assay. Consistently, OsWRKY80 exhibits transcriptional activation activity in a GAL4 assay in yeast cells. Overexpression of OsWRKY80 in rice plants significantly enhanced disease resistance to R. solani, concomitant with elevated expression of OsWRKY4, another positive regulator in rice defense against R. solani. Suppression of OsWRKY80 by RNA interference (RNAi), on the other hand, compromised disease resistance to R. solani. Results of yeast one-hybrid assay and transient expression assay in tobacco cells have revealed that OsWRKY80 specifically binds to the promoter regions of OsWRKY4, which contain W-box (TTGAC[C/T]) or W-box like (TGAC[C/T]) cis-elements.
We propose that OsWRKY80 functions upstream of OsWRKY4 as an important positive regulatory circuit that is implicated in rice defense response to sheath blight pathogen R. solani.
植物WRKY转录因子在多种生物学过程中发挥关键作用,尤其是在植物对病原体的防御反应中。纹枯病是水稻的主要病害之一。然而,我们对WRKY蛋白在水稻抗纹枯病中的功能了解相当有限。
在此我们证明,水稻纹枯病病原菌立枯丝核菌感染后,水稻WRKY80基因(OsWRKY80)的表达迅速且强烈地被诱导。OsWRKY80的表达也受到外源茉莉酸(JA)和乙烯(ET)的诱导,但不受水杨酸(SA)的诱导。在瞬时表达试验中,OsWRKY80 - GFP定位于洋葱表皮细胞的细胞核中。同样,在酵母细胞的GAL4试验中,OsWRKY80表现出转录激活活性。在水稻植株中过表达OsWRKY80显著增强了对立枯丝核菌的抗病性,同时水稻防御立枯丝核菌的另一个正向调节因子OsWRKY4的表达也有所升高。另一方面,通过RNA干扰(RNAi)抑制OsWRKY80会削弱对立枯丝核菌的抗病性。酵母单杂交试验和烟草细胞瞬时表达试验的结果表明,OsWRKY80特异性结合OsWRKY4的启动子区域,该区域含有W - box(TTGAC[C/T])或类W - box(TGAC[C/T])顺式元件。
我们提出,OsWRKY80在OsWRKY4的上游发挥作用,作为一个重要的正向调节回路,参与水稻对纹枯病病原菌立枯丝核菌的防御反应。