Direct protein interaction underlies gene-for-gene specificity and coevolution of the flax resistance genes and flax rust avirulence genes

被引:564
作者
Dodds, Peter N.
Lawrence, Gregory J.
Catanzariti, Ann-Maree
Teh, Trazel
Wang, Ching-I. A.
Ayliffe, Michael A.
Kobe, Bostjan
Ellis, Jeffrey G.
机构
[1] Commonwealth Sci & Ind Res Org Plant Ind, Canberra, ACT 2601, Australia
[2] Univ Queensland, Sch Mol & Microbial Sci, Brisbane, Qld 4072, Australia
[3] Univ Queensland, Inst Mol Biosci, Brisbane, Qld 4072, Australia
关键词
avirulence protein; resistance protein;
D O I
10.1073/pnas.0602577103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Plant resistance proteins (R proteins) recognize corresponding pathogen avirulence (Avr) proteins either indirectly through detection of changes in their host protein targets or through direct R-Avr protein interaction. Although indirect recognition imposes selection against Avr effector function, pathogen effector molecules recognized through direct interaction may overcome resistance through sequence diversification rather than loss of function. Here we show that the flax rust fungus AvrLS67 genes, whose products are recognized by the L5, L6, and L7 R proteins of flax, are highly diverse, with 12 sequence variants identified from six rust strains. Seven AvrL567 variants derived from Avr alleles induce necrotic responses when expressed in flax plants containing corresponding resistance genes (R genes), whereas five variants from avr alleles do not. Differences in recognition specificity between AvA567 variants and evidence for diversifying selection acting on these genes suggest they have been involved in a gene-specific arms race with the corresponding flax R genes. Yeast two-hybrid assays indicate that recognition is based on direct R-Avr protein interaction and recapitulate the interaction specificity observed in planta. Biochemical analysis of Escherichia coli-produced AvrL567 proteins shows that variants that escape recognition nevertheless maintain a conserved structure and stability, suggesting that the amino acid sequence differences directly affect the R-Avr protein interaction. We suggest that direct recognition associated with high genetic diversity at corresponding R and Avr gene loci represents an alternative outcome of plant-pathogen coevolution to indirect recognition associated with simple balanced polymorphisms for functional and nonfunctional R and Avr genes.
引用
收藏
页码:8888 / 8893
页数:6
相关论文
共 35 条
  • [1] Strategies used by bacterial pathogens to suppress plant defenses
    Abramovitch, RB
    Martin, GB
    [J]. CURRENT OPINION IN PLANT BIOLOGY, 2004, 7 (04) : 356 - 364
  • [2] Host-parasite coevolutionary conflict between Arabidopsis and downy mildew
    Allen, RL
    Bittner-Eddy, PD
    Grenvitte-Briggs, LJ
    Meitz, JC
    Rehmany, AP
    Rose, LE
    Beynon, JL
    [J]. SCIENCE, 2004, 306 (5703) : 1957 - 1960
  • [3] Gapped BLAST and PSI-BLAST: a new generation of protein database search programs
    Altschul, SF
    Madden, TL
    Schaffer, AA
    Zhang, JH
    Zhang, Z
    Miller, W
    Lipman, DJ
    [J]. NUCLEIC ACIDS RESEARCH, 1997, 25 (17) : 3389 - 3402
  • [4] EVALUATION OF SECONDARY STRUCTURE OF PROTEINS FROM UV CIRCULAR-DICHROISM SPECTRA USING AN UNSUPERVISED LEARNING NEURAL-NETWORK
    ANDRADE, MA
    CHACON, P
    MERELO, JJ
    MORAN, F
    [J]. PROTEIN ENGINEERING, 1993, 6 (04): : 383 - 390
  • [5] Initiation of RPS2-specified disease resistance in Arabidopsis is coupled to the AvrRpt2-directed elimination of RIN4
    Axtell, MJ
    Staskawicz, BJ
    [J]. CELL, 2003, 112 (03) : 369 - 377
  • [6] Constitutive gain-of-function mutants in a nucleotide binding site-leucine rich repeat protein encoded at the Rx locus of potato
    Bendahmane, A
    Farnham, G
    Moffett, P
    Baulcombe, DC
    [J]. PLANT JOURNAL, 2002, 32 (02) : 195 - 204
  • [7] An efficient system for high-level expression and easy purification of authentic recombinant proteins
    Catanzariti, AM
    Soboleva, TA
    Jans, DA
    Board, PG
    Baker, RT
    [J]. PROTEIN SCIENCE, 2004, 13 (05) : 1331 - 1339
  • [8] Physical interaction between RRS1-R, a protein conferring resistance to bacterial wilt, and PopP2, a type III effector targeted to the plant nucleus
    Deslandes, L
    Olivier, J
    Peeters, N
    Feng, DX
    Khounlotham, M
    Boucher, C
    Somssich, I
    Genin, S
    Marco, Y
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (13) : 8024 - 8029
  • [9] The Melampsora lini AvrL567 avirulence genes are expressed in haustoria and their products are recognized inside plant cells
    Dodds, PN
    Lawrence, GJ
    Catanzariti, AM
    Ayliffe, MA
    Ellis, JG
    [J]. PLANT CELL, 2004, 16 (03) : 755 - 768
  • [10] Dodds PN, 2000, MOL PLANT PATHOL, P88