The stem rust resistance gene Rpg5 encodes a protein with nucleotide-binding-site, leucine-rich, and protein kinase domains

R. Brueggeman, A. Druka, J. Nirmala, T. Cavileer, T. Drader, N. Rostoks, A. Mirlohi, H. Bennypaul, U. Gill, D. Kudrna, C. Whitelaw, A. Kilian, F. Han, Y. Sun, K. Gill, B. Steffenson, A. Kleinhofs

Research output: Contribution to journalArticlepeer-review

127 Scopus citations

Abstract

We isolated the barley stem rust resistance genes Rpg5 and rpg4 by map-based cloning. These genes are colocalized on a 70-kb genomic region that was delimited by recombination. The Rpg5 gene consists of an unusual structure encoding three typical plant disease resistance protein domains: nucleotide-binding site, leucine-rich repeat, and serine threonine protein kinase. The predicted RPG5 protein has two putative transmembrane sites possibly involved in membrane binding. The gene is expressed at low but detectable levels. Posttranscriptional gene silencing using VIGS resulted in a compatible reaction with a normally incompatible stem rust pathogen. Allele sequencing also validated the candidate Rpg5 gene. Allele and recombinant sequencing suggested that the probable rpg4 gene encoded an actin depolymerizing factor-like protein. Involvement of actin depolymerizing factor genes in nonhost resistance has been documented, but discovery of their role in gene-for-gene interaction would be novel and needs to be further substantiated.

Original languageEnglish (US)
Pages (from-to)14970-14975
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume105
Issue number39
DOIs
StatePublished - Sep 30 2008

Keywords

  • Actin depolymerizing factor
  • Barley
  • Disease resistance domains
  • Map-based cloning

ASJC Scopus subject areas

  • General

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