Literature DB >> 7556057

The race-specific elicitor, NIP1, from the barley pathogen, Rhynchosporium secalis, determines avirulence on host plants of the Rrs1 resistance genotype.

M Rohe1, A Gierlich, H Hermann, M Hahn, B Schmidt, S Rosahl, W Knogge.   

Abstract

NIP1, a small phytotoxic protein secreted by the barley pathogen Rhynchosporium secalis, is a race-specific elicitor of defense responses in barley cultivars carrying the resistance gene, Rrs1. Co-inoculation employing spores from a virulent fungal race together with the NIP1 protein converted the phenotype of the interaction from compatible to incompatible only on Rrs1-containing plants. In addition, transformation of a virulent fungal race with the nip1 gene yielded avirulent transformants. This demonstrated that the protein is the product of a fungal avirulence gene. The fungal genome was found to contain a single copy of the nip1 gene. Sequence analysis of nip1 cDNA and genomic clones revealed that the gene consists of two exons and one intron. The derived amino acid sequence comprised a secretory signal peptide of 22 amino acids and a cysteine-rich mature protein of 60 amino acids. All fungal races that were avirulent on barley cultivars of the Rrs1 resistance genotype carry and express the nip1 gene and secrete an elicitor-active NIP1 polypeptide. In contrast, races lacking this gene were virulent. In addition, single nucleotide exchanges were detected in the coding region of the nip1 alleles in one virulent fungal race and in a race whose interaction with barley is not controlled by the Rrs1 gene. The resulting exchanges of single amino acids render the gene products elicitor-inactive. Thus, the R.secalis-barley interaction provides the first example of a pathosystem conforming to the gene-for-gene hypothesis in which a plant with a particular resistance gene recognizes a pathogen by a virulence factor, i.e. one of its offensive weapons. On the fungal side, in turn, recognition by the host plant is eluded by either deletion of the encoding gene or alteration of the primary structure of the gene product.

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Year:  1995        PMID: 7556057      PMCID: PMC394499          DOI: 10.1002/j.1460-2075.1995.tb00090.x

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  27 in total

1.  Function of rodlets on the surface of fungal spores.

Authors:  R E Beever; G P Dempsey
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Review 2.  The molecular biology of disease resistance.

Authors:  N T Keen
Journal:  Plant Mol Biol       Date:  1992-05       Impact factor: 4.076

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Authors:  J Logemann; J Schell; L Willmitzer
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Review 4.  Direct sequencing of polymerase chain reaction-amplified DNA.

Authors:  V B Rao
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5.  Supercoil sequencing: a fast and simple method for sequencing plasmid DNA.

Authors:  E Y Chen; P H Seeburg
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6.  Rapid isolation of high molecular weight plant DNA.

Authors:  M G Murray; W F Thompson
Journal:  Nucleic Acids Res       Date:  1980-10-10       Impact factor: 16.971

7.  Cloning and characterization of cDNA of avirulence gene avr9 of the fungal pathogen Cladosporium fulvum, causal agent of tomato leaf mold.

Authors:  J A van Kan; G F van den Ackerveken; P J de Wit
Journal:  Mol Plant Microbe Interact       Date:  1991 Jan-Feb       Impact factor: 4.171

8.  The Neurospora circadian clock-controlled gene, ccg-2, is allelic to eas and encodes a fungal hydrophobin required for formation of the conidial rodlet layer.

Authors:  D Bell-Pedersen; J C Dunlap; J J Loros
Journal:  Genes Dev       Date:  1992-12       Impact factor: 11.361

9.  Molecular analysis of the avirulence gene avr9 of the fungal tomato pathogen Cladosporium fulvum fully supports the gene-for-gene hypothesis.

Authors:  G F Van den Ackerveken; J A Van Kan; P J De Wit
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10.  Host range of a plant pathogenic fungus determined by a saponin detoxifying enzyme.

Authors:  P Bowyer; B R Clarke; P Lunness; M J Daniels; A E Osbourn
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  42 in total

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Authors:  J Chamnanpunt; W X Shan; B M Tyler
Journal:  Proc Natl Acad Sci U S A       Date:  2001-11-27       Impact factor: 11.205

2.  Predicting durability of a disease resistance gene based on an assessment of the fitness loss and epidemiological consequences of avirulence gene mutation.

Authors:  C M Vera Cruz; J Bai; I Ona; H Leung; R J Nelson; T W Mew; J E Leach
Journal:  Proc Natl Acad Sci U S A       Date:  2000-12-05       Impact factor: 11.205

3.  Molecular mapping of two cultivar-specific avirulence genes in the rice blast fungus Magnaporthe grisea.

Authors:  Q H Chen; Y C Wang; A N Li; Z G Zhang; X B Zheng
Journal:  Mol Genet Genomics       Date:  2006-11-07       Impact factor: 3.291

4.  Fine mapping, physical mapping and development of diagnostic markers for the Rrs2 scald resistance gene in barley.

Authors:  Anja Hanemann; Günther F Schweizer; Roberto Cossu; Thomas Wicker; Marion S Röder
Journal:  Theor Appl Genet       Date:  2009-09-25       Impact factor: 5.699

5.  Amplification generates modular diversity at an avirulence locus in the pathogen Phytophthora.

Authors:  Rays H Y Jiang; Rob Weide; Peter J I van de Vondervoort; Francine Govers
Journal:  Genome Res       Date:  2006-07       Impact factor: 9.043

6.  Three genes of the Arabidopsis RPP1 complex resistance locus recognize distinct Peronospora parasitica avirulence determinants.

Authors:  M A Botella; J E Parker; L N Frost; P D Bittner-Eddy; J L Beynon; M J Daniels; E B Holub; J D Jones
Journal:  Plant Cell       Date:  1998-11       Impact factor: 11.277

Review 7.  Programmed cell death in the plant immune system.

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Journal:  Cell Death Differ       Date:  2011-04-08       Impact factor: 15.828

Review 8.  The role of the plasma membrane H+-ATPase in plant-microbe interactions.

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Journal:  Mol Plant       Date:  2011-02-07       Impact factor: 13.164

9.  A single binding site mediates resistance- and disease-associated activities of the effector protein NIP1 from the barley pathogen Rhynchosporium secalis.

Authors:  Klaas A E van't Slot; Angela Gierlich; Wolfgang Knogge
Journal:  Plant Physiol       Date:  2007-05-03       Impact factor: 8.340

10.  Correlation between binding affinity and necrosis-inducing activity of mutant AVR9 peptide elicitors.

Authors:  M Kooman-Gersmann; R Vogelsang; P Vossen; H W van den Hooven; E Mahé; G Honée; P J de Wit
Journal:  Plant Physiol       Date:  1998-06       Impact factor: 8.340

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