scholarly journals Direct interaction of resistance gene and avirulence gene products confers rice blast resistance

2000 ◽  
Vol 19 (15) ◽  
pp. 4004-4014 ◽  
Author(s):  
Yulin Jia ◽  
Sean A. McAdams ◽  
Gregory T. Bryan ◽  
Howard P. Hershey ◽  
Barbara Valent
2000 ◽  
Vol 12 (11) ◽  
pp. 2019 ◽  
Author(s):  
Marc J. Orbach ◽  
Leonard Farrall ◽  
James A. Sweigard ◽  
Forrest G. Chumley ◽  
Barbara Valent

2000 ◽  
Vol 12 (11) ◽  
pp. 2019-2032 ◽  
Author(s):  
Marc J. Orbach ◽  
Leonard Farrall ◽  
James A. Sweigard ◽  
Forrest G. Chumley ◽  
Barbara Valent

Crop Science ◽  
2016 ◽  
Vol 56 (3) ◽  
pp. 1001-1008 ◽  
Author(s):  
Yan Liu ◽  
Yulin Jia ◽  
David Gealy ◽  
David M. Goad ◽  
Ana L. Caicedo ◽  
...  

2015 ◽  
Vol 5 (1) ◽  
Author(s):  
Kumar Vasudevan ◽  
Wilhelm Gruissem ◽  
Navreet K. Bhullar

Abstract Rice blast is one of the most devastating rice diseases and continuous resistance breeding is required to control the disease. The rice blast resistance gene Pi54 initially identified in an Indian cultivar confers broad-spectrum resistance in India. We explored the allelic diversity of the Pi54 gene among 885 Indian rice genotypes that were found resistant in our screening against field mixture of naturally existing M. oryzae strains as well as against five unique strains. These genotypes are also annotated as rice blast resistant in the International Rice Genebank database. Sequence-based allele mining was used to amplify and clone the Pi54 allelic variants. Nine new alleles of Pi54 were identified based on the nucleotide sequence comparison to the Pi54 reference sequence as well as to already known Pi54 alleles. DNA sequence analysis of the newly identified Pi54 alleles revealed several single polymorphic sites, three double deletions and an eight base pair deletion. A SNP-rich region was found between a tyrosine kinase phosphorylation site and the nucleotide binding site (NBS) domain. Together, the newly identified Pi54 alleles expand the allelic series and are candidates for rice blast resistance breeding programs.


2008 ◽  
Vol 21 (4) ◽  
pp. 396-403 ◽  
Author(s):  
Yulin Jia ◽  
Rodger Martin

Resistance to the blast pathogen Magnaporthe oryzae is proposed to be initiated by physical binding of a putative cytoplasmic receptor encoded by a nucleotide binding site-type resistance gene, Pi-ta, to the processed elicitor encoded by the corresponding avirulence gene AVR-Pita. Here, we report the identification of a new locus, Ptr(t), that is required for Pi-ta–mediated signal recognition. A Pi-ta–expressing susceptible mutant was identified using a genetic screen. Putative mutations at Ptr(t) do not alter recognition specificity to another resistance gene, Pi-ks, in the Pi-ta homozygote, indicating that Ptr(t) is more likely specific to Pi-ta–mediated signal recognition. Genetic crosses of Pi-ta Ptr(t) and Pi-ta ptr(t) homozygotes suggest that Ptr(t) segregates as a single dominant nuclear gene. A ratio of 1:1 (resistant/susceptible) of a population of BC1 of Pi-ta Ptr(t) with pi-ta ptr(t) homozygotes indicates that Pi-ta and Ptr(t) are linked and cosegregate. Genotyping of mutants of pi-ta ptr(t) and Pi-ta Ptr(t) homozygotes using ten simple sequence repeat markers at the Pi-ta region determined that Pi-ta and Ptr(t) are located within a 9-megabase region and are of indica origin. Identification of Ptr(t) is a significant advancement in studying Pi-ta–mediated signal recognition and transduction.


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