Kim Kang-Chang, Lai Zhibing, Fan Baofang, Chen Zhixiang
Department of Botany and Plant Pathology, Purdue University, West Lafayette, Indiana 47907-2054, USA.
Plant Cell. 2008 Sep;20(9):2357-71. doi: 10.1105/tpc.107.055566. Epub 2008 Sep 5.
Arabidopsis thaliana WRKY38 and WRKY62, encoding two structurally similar type III WRKY transcription factors, are induced in a Nonexpressor of PR Gene1 (NPR1)-dependent manner by salicylic acid (SA) or by virulent Pseudomonas syringae. Disease resistance and SA-regulated Pathogenesis-Related1 (PR1) gene expression are enhanced in the wrky38 and wrky62 single mutants and, to a greater extent, in the double mutants. Overexpression of WRKY38 or WRKY62 reduces disease resistance and PR1 expression. Thus, WRKY38 and WRKY62 function additively as negative regulators of plant basal defense. WRKY38 and WRKY62 interact with Histone Deacetylase 19 (HDA19). Expression of HDA19 is also induced by P. syringae, and the stability of its induced transcripts depends on SA and NPR1 in infected plants. Disruption of HDA19 leads to compromised resistance, whereas its overexpression results in enhanced resistance to P. syringae. Thus, HDA19 has a role opposite from those of WRKY38 and WRKY62 in basal resistance to the bacterial pathogen. Both WRKY38 and WRKY62 are transcriptional activators in plant cells, but their activation activities are abolished by overexpressed HDA19. Interaction of WRKY38 and WRKY62 with HDA19 may act to fine-tune plant basal defense responses.
拟南芥WRKY38和WRKY62编码两个结构相似的III型WRKY转录因子,它们在水杨酸(SA)或毒性丁香假单胞菌的诱导下,以依赖病程相关基因1非表达子(NPR1)的方式被诱导表达。在wrky38和wrky62单突变体中,抗病性和SA调节的病程相关蛋白1(PR1)基因表达增强,在双突变体中增强程度更大。WRKY38或WRKY62的过表达降低了抗病性和PR1表达。因此,WRKY38和WRKY62作为植物基础防御的负调控因子发挥累加作用。WRKY38和WRKY62与组蛋白去乙酰化酶19(HDA19)相互作用。HDA19的表达也受到丁香假单胞菌的诱导,其诱导转录本的稳定性在受感染植物中依赖于SA和NPR1。HDA19的破坏导致抗性受损,而其过表达导致对丁香假单胞菌的抗性增强。因此,HDA19在对细菌病原体的基础抗性中具有与WRKY38和WRKY62相反的作用。WRKY38和WRKY62在植物细胞中都是转录激活因子,但它们的激活活性被过表达的HDA19消除。WRKY38和WRKY62与HDA19的相互作用可能起到微调植物基础防御反应的作用。