Jin Lian, Qin Qingqing, Wang Yu, Pu Yingying, Liu Lifang, Wen Xing, Ji Shaoyi, Wu Jianguo, Wei Chunhong, Ding Biao, Li Yi
The State Key Laboratory of Protein and Plant Gene Research, College of Life Sciences, Peking University, Beijing, People's Republic of China.
Department of Molecular Genetics and Center for RNA Biology, The Ohio State University, Columbus, Ohio, United States of America.
PLoS Pathog. 2016 Sep 8;12(9):e1005847. doi: 10.1371/journal.ppat.1005847. eCollection 2016 Sep.
The phytohormone auxin plays critical roles in regulating myriads of plant growth and developmental processes. Microbe infection can disturb auxin signaling resulting in defects in these processes, but the underlying mechanisms are poorly understood. Auxin signaling begins with perception of auxin by a transient co-receptor complex consisting of an F-box transport inhibitor response 1/auxin signaling F-box (TIR1/AFB) protein and an auxin/indole-3-acetic acid (Aux/IAA) protein. Auxin binding to the co-receptor triggers ubiquitination and 26S proteasome degradation of the Aux/IAA proteins, leading to subsequent events, including expression of auxin-responsive genes. Here we report that Rice dwarf virus (RDV), a devastating pathogen of rice, causes disease symptoms including dwarfing, increased tiller number and short crown roots in infected rice as a result of reduced sensitivity to auxin signaling. The RDV capsid protein P2 binds OsIAA10, blocking the interaction between OsIAA10 and OsTIR1 and inhibiting 26S proteasome-mediated OsIAA10 degradation. Transgenic rice plants overexpressing wild-type or a dominant-negative (degradation-resistant) mutant of OsIAA10 phenocopy RDV symptoms are more susceptible to RDV infection; however, knockdown of OsIAA10 enhances the resistance of rice to RDV infection. Our findings reveal a previously unknown mechanism of viral protein reprogramming of a key step in auxin signaling initiation that enhances viral infection and pathogenesis.
植物激素生长素在调节众多植物生长和发育过程中发挥着关键作用。微生物感染会扰乱生长素信号传导,导致这些过程出现缺陷,但其潜在机制尚不清楚。生长素信号传导始于由F-box运输抑制剂响应1/生长素信号传导F-box(TIR1/AFB)蛋白和生长素/吲哚-3-乙酸(Aux/IAA)蛋白组成的瞬时共受体复合物对生长素的感知。生长素与共受体结合会触发Aux/IAA蛋白的泛素化和26S蛋白酶体降解,从而引发后续事件,包括生长素响应基因的表达。在这里,我们报告水稻矮缩病毒(RDV)是水稻的一种毁灭性病原体,由于对生长素信号的敏感性降低,在受感染的水稻中会导致矮化、分蘖数增加和冠根短等疾病症状。RDV衣壳蛋白P2与OsIAA10结合,阻断OsIAA10与OsTIR1之间的相互作用,并抑制26S蛋白酶体介导的OsIAA10降解。过表达野生型或显性负性(抗降解)突变体OsIAA10的转基因水稻植株表现出与RDV症状相似的表型,且对RDV感染更敏感;然而,敲低OsIAA10可增强水稻对RDV感染的抗性。我们的研究结果揭示了一种以前未知的病毒蛋白对生长素信号起始关键步骤进行重编程的机制,该机制增强了病毒感染和发病机制。