Skip to main content
Log in

Genetic and physical mapping of AvrPi7, a novel avirulence gene of Magnaporthe oryzae using physical position-ready markers

  • Articles
  • Published:
Chinese Science Bulletin

Abstract

Rice blast, caused by the fungal pathogen Magnaporthe oryzae, is one of the most devastating crop diseases worldwide. The avirulence gene corresponding to rice blast resistance gene Pi7 in field isolate CHL346 was inherited as a single gene, designated AvrPi7, in a segregating population consisting of 189 ascospore progenies derived from a cross between field isolates CHL346 and CHL42. In order to determine the chromosomal location of the AvrPi7 locus, a total of 121 simple sequence repeat (SSR) markers were developed based on the whole-genome sequence of reference isolate 70-15 of M. oryzae. Linkage analysis of the locus with these SSR markers showed that eight SSR markers on chromosome 1 were linked to the locus, among which the closest flanking markers MS1-9 and MS1-15 were 3.2 and 16.4 cM from the locus, respectively. For fine mapping, additional PCR-based makers including eight SSR markers and three candidate avirulence gene (CAG) markers were developed in the region flanking both markers. The AvrPi7 locus was genetically delimited within a 1.6-cM region flanked by markers MS1-21 and MS1-22, and co-segregated with the marker CAG2. To construct a physical map of the AvrPi7 locus, molecular markers linked to the Avr gene were mapped on the supercontigs of the reference isolate 70-15 through bioinformation analysis (BIA). Consequently, the AvrPi7 locus was delimited to a 75-kb interval flanked by markers MS1-21 and MS1-22 based on the reference sequence. Merodiploids observed in this study are also discussed.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Ou S H. Rice Diseases. 2nd ed. Surrey, England: Commonwealth Mycological Institute, 1985. 109–201

    Google Scholar 

  2. Dean R A, Talbot N J, Ebbole D J, et al. The genome sequence of the rice blast fungus Magnaporthe grisea. Nature, 2005, 434: 980–986

    Article  Google Scholar 

  3. Luo C X, Yin L F, Koyanagi S, et al. Genetic mapping and chromosomal assignment of Magnaporthe oryzae avrirulence genes AvrPik, AvrPiz, and AvrPiz-t controlling cultivar specificity on rice. Phypathology, 2005, 95: 640–647

    Google Scholar 

  4. Flor H. Current status of the gene-for-gene concept. Annu Rev Phytopathol, 1971, 9: 275–296

    Article  Google Scholar 

  5. Herbert T T. The perfect stage of Pyricularia grisea. Phytopathology, 1971, 61: 83–87

    Article  Google Scholar 

  6. Notteghem J L, Tharreau D, Silue D, et al. Present knowledge of rice resistance genetics and strategies for Magnaporthe grisea pathogenicity and avirulence gene analysis. In: Zeigler R S, Leong S A, Teng P S, eds. Rice Blast Disease. Walliingford: CAB International, 1994. 155–165

    Google Scholar 

  7. Leung H, Williams P H. Genetic analyses of electrophoretic enzyme variants, mating type, and hermaphroditism in Pyricularia oryzae Cavara. Can J Genet Cytol, 1985, 27: 697–704

    Google Scholar 

  8. Leung H, Borromeo E S, Bernardo M A, et al. Genetic analysis of virulence in the rice blast fungus Magnaporthe grisea. Phytopathology, 1988, 78: 1227–1233

    Google Scholar 

  9. Farman M L, Leong S A. Chromosome walking to AVR1-CO39 avirulence gene of Magnaporthe grisea discrepancy between the physical and genetic maps. Genetics, 1998, 150: 1049–1058

    Google Scholar 

  10. Smith J R, Leong S A. Mapping of Magnaporthe grisea locus affecting rice (Oryza sativa) cultivar specifity. Theor Appl Genet, 1994, 88: 901–908

    Article  Google Scholar 

  11. Lau G W, Chao C T, Ellingboe A H. Interaction of genes controlling avirulence/virulence of Magnaporthe grisea on rice cultivar Katy. Phytopathology, 1993, 83: 375–382

    Article  Google Scholar 

  12. Silué D, Tharreau D, Notteghem J L. Identification of Magnaporthe grisea avirulence genes to seven rice cultivars. Phytopathology, 1992, 82: 1462–1467

    Google Scholar 

  13. Dioh W, Tharreau D, Notteghem J L, et al. Mapping of avirulence genes in the rive blast fungus, Magnaporthe grisea, with RFLP and RAPD markers. Mol Plant Microbe Interact, 2000, 13: 217–227

    Google Scholar 

  14. Wang B H, Lu G D, Lin W M, et al. Genetic analysis and molecular marker of Avr-Pi1, Avr-Pi2 and Avr-Pi4a of Magnaporthe grisea. Acta Genet Sin (in Chinese), 2002, 29: 820–826

    Google Scholar 

  15. Li C Y, Luo C X, Li J B, et al. Mapping avirulence gene in the rice blast fungus Magnaporthe grisea. Sci Agr Sin (in Chinese), 2000, 33: 49–53

    Google Scholar 

  16. Lin F, Li J B, Li C Y, et al. Identification of two avirulence genes in the rice blast fungus Magnaporthe grisea using random amplified polymorphic DNA (RAPD) markers. Sci Agr Sin (in Chinese), 2002, 35: 1079–1084

    Google Scholar 

  17. Hayashi N, Li C Y, Li J R, Naito H. In vitro production on rice plants of perithecia of Magnaporthe grisea from Yunnan, China. Mycol Res, 1997, 101: 1308–1310

    Article  Google Scholar 

  18. Valent B, Chumley F G. Avirulence genes and mechanisms of genetic instability in the rice blast fungus. In: Zeigler R, Leong S A, Teng P S, eds. Rice Blast Disease. Wallingford: CAB International, 1994. 111–134

    Google Scholar 

  19. Valent B, Chumley F G. Molecular genetic analysis of the rice blast fungus, Magnaporthe grisea. Annu Rev Phytopathol, 1991, 29: 443–467

    Article  Google Scholar 

  20. Yasuda N, Fujita Y, Noguchi M. Identification of avirulence genes in the rice blast fungus corresponding to three resistance genes in Japanese differentials. J Gen Plant Pathol, 2004, 70: 202–206

    Article  Google Scholar 

  21. Yasuda N, Noguchi M T, Fijita Y. Identification of an avirulence gene in the fungus Magnaporthe grisea corresponding to a resistance gene at the Pik locus. Phytopathology, 2005, 95: 768–772

    Google Scholar 

  22. Liu J F, Dong N, Hou Z J, et al. Identification of a RAPD markers linked with the locus in rice blast fungus conferring avirulence to rice cultivar Tsuyuke. Acta Phytopathol Sin (in Chinese), 2001, 31: 10–15

    Google Scholar 

  23. Orbach M J, Farrall L, Sweigard J A, et al. A telomeric avirulence gene determines efficacy for the rice blast resistance gene Pi-ta. Plant Cell, 2000, 12: 2019–2032

    Article  Google Scholar 

  24. Böhnert H U, Fudal I, Dioh W, et al. A putative polyketide synthase/peptide synthetae from Magnaporthe grisea signals pathogen attack to resistance rice. Plant cell, 2004, 16: 2499–2513

    Article  Google Scholar 

  25. Lauge R, De Wit P J G M. Fungal avirulence genes: Structure and possible functions. Fungal Genet Biol, 1998, 24: 285–297

    Article  Google Scholar 

  26. Ma J H, Wang L, Feng S J, et al. Identification and fine mapping of AvrPi15, a novel avirulence gene of Magnaporthe grisea. Theor Appl Genet, 2006, 113: 875–883

    Article  Google Scholar 

  27. Pan Q H, Hu Z D, Tanisaka T, et al. Fine mapping of the blast resistance gene Pi15, linked to Pii, on rice chromosome 9. Acta Bot Sin, 2003, 45: 871–877

    Google Scholar 

  28. Tsunematsu H, Yanoria M J T, Ebron L A, et al. Development of monogenic lines of rice for blast resistance. Breed Sci, 2000, 50: 229–234

    Google Scholar 

  29. Pan Q H, Wang L, Ikehashi H, et al. Identification of a new blast resistance gene in the indica rice cultivar Kasalath using Japanese differential cultivars and isozyme markers. Phytopathology, 1996, 86: 1071–1075

    Article  Google Scholar 

  30. Farman M L, Eto Y, Nakao T, et al. Analysis of the structure of the AVR1-CO39 avirulence locus in virulent rice-infecting isolates of Magnaporthe grisea. Mol Plant Microbe Interact, 2002, 15: 6–16

    Google Scholar 

  31. Chen S, Wang L, Que Z Q, et al. Genetic and physical mapping of Pi37(t), a new gene conferring resistance to rice blast in the famous cultivar St.No.1. Theor Appl Genet, 2005, 111: 1563–1570

    Article  Google Scholar 

  32. Liu X Q, Wang L, Chen S, et al. Genetic and physical mapping of Pi36(t), a new rice blast resistance gene located on rice chromosome 8. Mol Gen Genomics, 2005, 274: 394–401

    Article  Google Scholar 

  33. Chen J W, Pang X F, Wang L, et al. Genetic analysis and fine mapping of a rice brown planthopper (Nilaparvata lugens Stål) resistance gene bph19(t). Mol Genet Genomics, 2006, 275: 321–329

    Article  Google Scholar 

  34. Michelmore R W, Paran I, Kesseli R V. Identification of markers linked to disease resistance genes by bulked segregant analysis: A rapid method to detect markers in specific genomic regions by using segregating populations. Proc Natl Acad Sci USA, 1991, 88: 9828–9832

    Article  Google Scholar 

  35. Tanksley S D, Ganal M W, Martin G B. chromosome landing: A paradigm for map-based gene cloning in plants with large genomes. Trends Genet, 1995, 11: 63–68

    Article  Google Scholar 

  36. Joosten M H A J, Cozijnsen T J, De Wit P J G M. Host resistance to a fungal tomato pathogen lost by a single base-pair change in an avirulence gene. Nature, 1994, 367: 384–386

    Article  Google Scholar 

  37. Sweigard J A, Carroll A M, Kang S, et al. Identification, cloning, and characterization of PWL2, a gene for host species specificity in the rice blast fungus. Plant Cell, 1995, 7: 1221–1233

    Article  Google Scholar 

  38. Shan W X, Cao M, Leung D, et al. The Avr1b locus of Phytophthora sojae encodes an elicitor and a regulator required for avirulence on soybean plants carrying resistance gene Rps1b. Mol Plant Micobe Interact, 2004, 17: 394–403

    Google Scholar 

  39. Gout L, Fudal I, Kuhn M L, et al. Lost in the middle of nowhere: The AvrLm1 avirulence gene of the Dothideomycete Leptosphaeria maculans. Mol Microbiol, 2006, 60: 67–80

    Article  Google Scholar 

  40. Schuler G D. Sequence mapping by electronic PCR. Genome Res, 1997, 7: 541–550

    Google Scholar 

  41. Davis C R, Kempainen R R, Srodfs M S, et al. Correlation of the physical and genetic maps of the centromere region of the right arm of linkage group III of Neurospora crassa. Genetics, 1994, 136, 1297–1306

    Google Scholar 

  42. Chauhan R S, Farman M L, Zhang H B, et al. Genetic and physical mapping of a rice blast resistance locus, Pi-CO39(t), that corresponds to the avirulence gene AVR1-CO39 of Magnaporthe grisea. Mol Gen Genomics, 2002, 26: 603–612

    Article  Google Scholar 

  43. Clarke L, Carbon J. Isolation of the centromere-linked CDC10 gene by complementation in yeast. Proc Natl Acad Sci, USA, 1980, 77: 2173–2177

    Article  Google Scholar 

  44. Wu W H, Wang L, Pan Q H. Comparison of genetic structures of two rice blast fungus populations originated from Jiangsu and Yunnan Provinces, China. Chin J Tropical Crops (in Chinese), 2006, 17: 95–100

    Google Scholar 

  45. Sun X, Yang Z, Wang S, et al. Identification of a 47-kb DNA fragment containing Xa4, a locus for bacterial blight resistance in rice. Theor Appl Genet, 2003, 106: 683–687

    Google Scholar 

  46. Nitta N, Farman M L, Leong S A. Genome organization of Magnaporthe grisea: Integration of genetic maps, clustering of transposable elements and identification of genome duplications and rearrangements. Theor Appl Genet, 1997, 95: 20–32

    Article  Google Scholar 

  47. Hartl D L, Jones E W. Genetics: Analysis of Genes and Genomes. 5th ed. Boston: Jones and Bartlett Publishers, 2001. 393–443

    Google Scholar 

  48. Covert S F. Supernumerary chromosomes in filamentous fungi. Curr Genet, 1998, 33: 311–319

    Article  Google Scholar 

  49. Orbach M J, Chumley F G, Valent B. Electrophoretic karyotypes of Magnaporthe grisea pathogens of diverse grasses. Mol Plant Microbe Interact, 1996, 9: 261–271

    Google Scholar 

  50. Talbot N J, Salch Y P, Ma M, et al. Karyotypic variation within clonal lineages of the rice blast fungus, Magnaporth grisea. Appl Environ Microbiol, 1993, 59: 585–593

    Google Scholar 

  51. Chuma I, Tosa Y, Taga M, et al. Meiotic behavior of a supernumerary chromosome in Magnaporthe oryzae. Curr Genetic, 2003, 43: 191–198

    Google Scholar 

  52. Enkerli J, Reed H, Briley A, et al. Physical map of a conditionally dispensable chromosome in Nectria haematococca mating population VI and location of chromosome breakpoints. Genetics, 2000, 155: 1083–1094

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Pan QingHua.

Additional information

Supported by the National Basic Research Program of China (Grant No. 2006CB100206), the Program for Changjiang Scholars and Innovation Research Team in University (Grant No. IRT0448), and the Natural Science Foundation of Guangdong Province (Grant Nos. 021006 and 039254)

About this article

Cite this article

Feng, S., Wang, L., Ma, J. et al. Genetic and physical mapping of AvrPi7, a novel avirulence gene of Magnaporthe oryzae using physical position-ready markers. CHINESE SCI BULL 52, 903–911 (2007). https://doi.org/10.1007/s11434-007-0125-0

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11434-007-0125-0

Keywords

Navigation