| Literature DB >> 27861989 |
Haitao Cui1, Enrico Gobbato1, Barbara Kracher1, Jingde Qiu1, Jaqueline Bautor1, Jane E Parker1.
Abstract
Plant defenses induced by salicylic acid (SA) are vital for resistance against biotrophic pathogens. In basal and receptor-triggered immunity, SA accumulation is promoted by Enhanced Disease Susceptibility1 with its co-regulator Phytoalexin Deficient4 (EDS1/PAD4). Current models position EDS1/PAD4 upstream of SA but their functional relationship remains unclear. In a genetic and transcriptomic analysis of Arabidopsis autoimmunity caused by constitutive or conditional EDS1/PAD4 overexpression, intrinsic EDS1/PAD4 signaling properties and their relation to SA were uncovered. A core EDS1/PAD4 pathway works in parallel with SA in basal and effector-triggered bacterial immunity. It protects against disabled SA-regulated gene expression and pathogen resistance, and is distinct from a known SA-compensatory route involving MAPK signaling. Results help to explain previously identified EDS1/PAD4 regulated SA-dependent and SA-independent gene expression sectors. Plants have evolved an alternative route for preserving SA-regulated defenses against pathogen or genetic perturbations. In a proposed signaling framework, EDS1 with PAD4, besides promoting SA biosynthesis, maintains important SA-related resistance programs, thereby increasing robustness of the innate immune system.Entities:
Keywords: zzm321990Arabidopsis thalianazzm321990; RNA-seq; basal immunity; biotic stress network; effector-triggered immunity (ETI); transcriptional reprogramming
Mesh:
Substances:
Year: 2016 PMID: 27861989 DOI: 10.1111/nph.14302
Source DB: PubMed Journal: New Phytol ISSN: 0028-646X Impact factor: 10.151