Transposon tagging of tobacco mosaic virus resistance gene N: its possible role in the TMV-N-mediated signal transduction pathway

Proc Natl Acad Sci U S A. 1995 May 9;92(10):4175-80. doi: 10.1073/pnas.92.10.4175.

Abstract

Plants can recognize and resist invading pathogens by signaling the induction of rapid defense responses. Often these responses are mediated by single dominant resistance genes (R genes). The products of R genes have been postulated to recognize the pathogen and trigger rapid host defense responses. Here we describe isolation of the classical resistance gene N of tobacco that mediates resistance to the well-characterized pathogen tobacco mosaic virus (TMV). The N gene was isolated by transposon tagging using the maize Activator (Ac) transposon. We confirmed isolation of the N gene by complementation of the TMV-sensitive phenotype with a genomic DNA fragment. Sequence analysis of the N gene shows that it encodes a protein with an amino-terminal domain similar to that of the cytoplasmic domains of the Drosophila Toll protein and the interleukin 1 receptor in mammals, a putative nucleotide-binding site and 14 imperfect leucine-rich repeats. The presence of these functional domains in the predicted N gene product is consistent with the hypothesis that the N resistance gene functions in a signal transduction pathway. Similarities of N to Toll and the interleukin 1 receptor suggest a similar signaling mechanism leading to rapid gene induction and TMV resistance.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Consensus Sequence
  • DNA Transposable Elements*
  • Drosophila / genetics
  • Genes, Plant*
  • Immunity, Innate / genetics
  • Molecular Sequence Data
  • Mutagenesis, Insertional
  • Nicotiana / genetics*
  • Nicotiana / virology*
  • Phenotype
  • Plants, Toxic*
  • Repetitive Sequences, Nucleic Acid
  • Sequence Homology, Nucleic Acid
  • Signal Transduction*
  • Tobacco Mosaic Virus / genetics
  • Tobacco Mosaic Virus / pathogenicity*
  • Zea mays / genetics

Substances

  • DNA Transposable Elements