Dale Bumpers National Rice Research Center Site Logo
ARS Home About Us Helptop nav spacerContact Us En Espanoltop nav spacer
Printable VersionPrintable Version     E-mail this pageE-mail this page
Agricultural Research Service United States Department of Agriculture
Search
  Advanced Search
 
Programs and Projects
Subjects of Investigation
Germplasm Evaluation and Enhancement
Genomics Core Facility
Molecular Genetics
Molecular Plant Pathology
Molecular Biology
Cytogenetics
Weed Physiology
Cereal Chemistry
Rice Genetics and Breeding
 

Title: MOLECULAR CHARACTERIZATION OF MAGNAPORTHE GRISEA AVIRULENCE AVR-PITA ALLELES IN US PATHOTYPES

Authors
item Crowley, Eugenia
item Singh, P - UA RREC
item Correll, J - UNIV ARK, FAYETTEVILLE
item Jia, Yulin
item Rutger, J

Submitted to: American Phytopathological Society Annual Meeting
Publication Type: Abstract Only
Publication Acceptance Date: June 30, 2004
Publication Date: July 30, 2004
Citation: Winston, E.M., Singh, P., Correll, J., Jia, Y., Rutger, J.N. 2004. Molecular characterization of Magnaporthe grisea avirulence AVR-Pita alleles in US pathotypes. American Phytopathological Society Annual Meeting. Phytopathology. 94(6):47.

Technical Abstract: The Pi-ta gene in rice confers resistance to Magnaporthe grisea isolates containing the corresponding avirulence gene AVR-Pita. Maintaining durable Pi-ta-mediated resistance is challenging due to the high degree of pathogenic variability and genetic instability of M. grisea. Genetic mapping demonstrated that the M. grisea AVR-Pita gene is closely linked to the telometric region residing on chromosome 3. Evidence suggests that a blast race TM2 can delete allelic sequences from its genome, thereby infecting Pi-ta containing rice cultivars. The objective of this study was to determine the functionality of AVR-Pita alleles in isolates of M. grisea races found in the Southern United States. Utilizing gene specific primers, the native promoter and coding regions of the AVR-Pita gene were amplified from cDNA and genomic clones of the M. grisea wild-type isolates 0-137 and ZN61 (race IB-49), respectively. Fragments were directionally cloned into the vector pBluescript SK+. Clones were analyzed by restriction digestion and PCR amplification using AVR-Pita gene specific primers. Clones homologous to AVR-Pita genomic sequence were subsequently transformed into the race-shift isolate TM2. Complementation studies will be subsequently performed by inoculating the recombinant pathogen onto Pi-ta containing rice cultivars.

   
 
 
Last Modified: 05/25/2013
ARS Home | USDA.gov | Site Map | Policies and Links 
FOIA | Accessibility Statement | Privacy Policy | Nondiscrimination Statement | Information Quality | USA.gov | White House