Literature DB >> 8097122

Gene-for-genes interactions between cotton R genes and Xanthomonas campestris pv. malvacearum avr genes.

R De Feyter1, Y Yang, D W Gabriel.   

Abstract

Six plasmid-borne avirulence (avr) genes were previously cloned from strain XcmH of the cotton pathogen, Xanthomonas campestris pv. malvacearum. We have now localized all six avr genes on the cloned fragments by subcloning and Tn5-gusA insertional mutagenesis. None of these avr genes appeared to exhibit exclusively gene-for-gene patterns of interactions with cotton R genes, and avrB4 was demonstrated to confer avr gene-for-R genes (plural) avirulence to X. c. pv. malvacearum on congenic cotton lines carrying either of two different resistance loci, B1 or B4. Furthermore, the B1 locus appeared to confer R gene-for-avr genes resistance to cotton against isogenic X. c. pv. malvacearum strains carrying any one of three avr genes: avrB4, avrb6, or avrB102. Restriction enzyme, Southern blot hybridization, and DNA sequence analyses showed that the XcmH avr genes are all highly similar to each other, to avrBs3 and avrBsP from the pepper pathogen X. c. pv. vesicatoria, and to the host-specific virulence gene pthA from the citrus pathogen X. citri. The XcmH avr genes differed primarily in the multiplicity of a tandemly repeated 102-base pair motif within the central portions of the genes, repeated from 14 to 23 times in members of this gene family. The complete nucleotide sequence of avrb6 revealed that it is 97% identical in DNA sequence to avrB4, avrBs3, avrBsP, and pthA and that 62-bp inverted terminal repeats mark the boundaries of homology between avrb6 and all members of this Xanthomonas virulence/avirulence gene family sequenced to date. The terminal 38 bp of both inverted repeats are highly similar to the 38-bp consensus terminal sequence of the Tn3 family of transposons. Up to 11 members of the avr gene family appear to be present in North American strains of X. c. pv. malvacearum, including XcmH. The high level of homology observed among these avr genes and their presence in multiple copies may explain the gene-for-genes interactions and also the observed high frequencies (10(-3) to 10(-4) per locus) of X. c. pv. malvacearum race change mutations. Five spontaneous race change mutants of XcmH suffered avr locus deletions, strongly indicating intergenic recombination as the primary mechanism for generating new races in X. c. pv. malvacearum.

Entities:  

Mesh:

Year:  1993        PMID: 8097122     DOI: 10.1094/mpmi-6-225

Source DB:  PubMed          Journal:  Mol Plant Microbe Interact        ISSN: 0894-0282            Impact factor:   4.171


  49 in total

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Authors:  B Yang; W Zhu; L B Johnson; F F White
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4.  Membrane localization of the S1 subunit of pertussis toxin in Bordetella pertussis and implications for pertussis toxin secretion.

Authors:  Karen M Farizo; Stefanie Fiddner; Anissa M Cheung; Drusilla L Burns
Journal:  Infect Immun       Date:  2002-03       Impact factor: 3.441

5.  Analysis of subassemblies of pertussis toxin subunits in vivo and their interaction with the ptl transport apparatus.

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6.  Analysis of relative levels of production of pertussis toxin subunits and Ptl proteins in Bordetella pertussis.

Authors:  Anissa M Cheung; Karen M Farizo; Drusilla L Burns
Journal:  Infect Immun       Date:  2004-04       Impact factor: 3.441

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8.  In planta horizontal transfer of a major pathogenicity effector gene.

Authors:  B El Yacoubi; A M Brunings; Q Yuan; S Shankar; D W Gabriel
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9.  The phenolic recognition profiles of the Agrobacterium tumefaciens VirA protein are broadened by a high level of the sugar binding protein ChvE.

Authors:  W T Peng; Y W Lee; E W Nester
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10.  Genomic localization of tomato genes that control a hypersensitive reaction to Xanthomonas campestris pv. vesicatoria (Doidge) dye.

Authors:  Z H Yu; J F Wang; R E Stall; C E Vallejos
Journal:  Genetics       Date:  1995-10       Impact factor: 4.562

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