Open AccessBarley RIC171 interacts with RACB in planta and supports entry of the powdery mildew fungus
Author(s) -
Schultheiss Holger,
Preuss Jutta,
Pircher Thomas,
Eichmann Ruth,
Hückelhoven Ralph
Publication year - 2008
Publication title -
cellular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.542
H-Index - 138
eISSN - 1462-5822
pISSN - 1462-5814
DOI - 10.1111/j.1462-5822.2008.01167.x
Subject(s) - blumeria graminis , biology , powdery mildew , ustilago , green fluorescent protein , cdc42 , amino acid , microbiology and biotechnology , peptide sequence , fusion protein , gtpase , biochemistry , gene , botany , plant disease resistance , recombinant dna
Summary RHO‐like GTPases of plants (ROPs, also called RACs) are involved in plant development and interaction with the environment. The barley ROP protein RACB is involved in susceptibility to the fungal pathogen Blumeria graminis f.sp. hordei ( Bgh ) . By screening barley sequence databases for potential protein interactors of plant RHO‐like proteins, we identified a ROP‐interactive CRIB (CDC42/RAC interactive binding) motif containing protein of 171 amino acids (RIC171). The protein interacted with constitutively activated RACB in a targeted yeast two‐hybrid assay. By use of split yellow fluorescing protein fusions, we demonstrated that RIC171 interacts with constitutively activated (CA) RACB‐G15V but not with dominant negative RACB‐T20N in planta . Transient overexpression of RIC171, similar to overexpression of CA RACB‐G15V, rendered epidermal cells more susceptible to penetration by Bgh . In contrast, expression of a 46‐amino‐acid RIC171‐CRIB peptide, which was sufficient to interact with CA RACB‐G15V, had a dominant negative effect and reduced susceptibility to Bgh . A red fluorescing DsRED–RIC171 fusion protein colocalized with green fluorescing GFP–RACB‐G15V at the cell periphery. Coexpression with CA RACB‐G15V but not with RACB‐T20N increased peripheral localization of DsRED–RIC171. Additionally, DsRED–RIC171 accumulated at sites of fungal attack, suggesting enhanced ROP activity at sites of attempted fungal penetration.