Light regulation of asexual development in the rice blast fungus, Magnaporthe oryzae

Fungal Genetics and Biology

Volumn 43, Issue 10, 2006, Pages 694-706

  Lee, Kwangwon ^a   Singh, Pratibha ^a   Chung, Wen Chuan ^a   Ash, Joshua ^a   Kim, Tae Sung ^a   Hang, Lisa ^a   Park, Sohyun ^a  

^a Department of Obstetrics Gynecology   (United States)

Author keywords

Asexual development; Conidiophore; Filamentous fungi; Light regulation; Magnaporthe grisea; Magnaporthe oryzae; Pyricularia oryzae; Spore release

Indexed keywords

ARTICLE; ASEXUAL REPRODUCTION; BLUE LIGHT; CONIDIUM; CONTROLLED STUDY; FUNGAL DEVELOPMENT; FUNGAL SPORE GERMINATION; FUNGUS HYPHAE; FUNGUS SPORE; LIGHT DARK CYCLE; MAGNAPORTHE; MAGNAPORTHE GRISEA; MAGNAPORTHE ORYZAE; NEUROSPORA CRASSA; NONHUMAN; PHOTOTROPISM; PRIORITY JOURNAL; RED LIGHT; RICE BLAST; SPOROGENESIS;

BLOTTING, SOUTHERN; FUNGAL PROTEINS; GENE EXPRESSION REGULATION, FUNGAL; HYPHAE; LIGHT; MAGNAPORTHE; MUTATION; ORYZA SATIVA; PHOTORECEPTORS, MICROBIAL; POLYMERASE CHAIN REACTION; REPRODUCTION, ASEXUAL; SPORES, FUNGAL;

FUNGI; MAGNAPORTHE GRISEA; MAGNAPORTHE ORYZAE; NEUROSPORA CRASSA;

EID: 33747893774     PISSN: 10871845     EISSN: 10960937     Source Type: Journal    
DOI: 10.1016/j.fgb.2006.04.005     Document Type: Article

References (75)

1. Ambra R., Grimaldi B., Zamboni S., Filetici P., Macino G., and Ballario P. Photomorphogenesis in the hypogeous fungus Tuber borchii: isolation and characterization of Tbwc-1, the homologue of the blue-light photoreceptor of Neurospora crassa. Fungal Genet. Biol. 41 (2004) 688-697
2. Ballario P., Vittorioso P., Magrelli A., Talora C., Cabibbo A., and Macino G. White collar-1, a central regulator of blue light responses in Neurospora, is a zinc finger protein. EMBO J. 15 (1996) 1650-1657
3. Barksdale T.H., and Asai G.N. Diurnal spore release of Piricularia oryzae from rice leaves. Phytopathology 51 (1961) 313-317
4. Belo I., Pinheiro R., and Mota M. Morphological and physiological changes in Saccharomyces cerevisiae by oxidative stress from hyperbaric air. J. Biotechnol. 115 (2005) 397-404
5. Blumenstein A., Vienken K., Tasler R., Purschwitz J., Veith D., Frankenberg-Dinkel N., and Fischer R. The Aspergillus nidulans phytochrome FphA represses sexual development in red light. Curr. Biol. 15 (2005) 1833-1838
6. Brooke P.J. Stimulation of ascospore release in Venturia inaequalis by far-red light. Nature 222 (1969) 390-392
7. Carroll A.M., Sweigard J.A., and Valent B. Improved vectors for selecting resistance to hygromycin. Fungal Genet. Newslett. 41 (1994) 21
8. Casas-Flores S., Rios-Momberg M., Bibbins M., Ponce-Noyola P., and Herrera-Estrella A. BLR-1 and BLR-2, key regulatory elements of photoconidiation and mycelial growth in Trichoderma atroviride. Microbiology 150 (2004) 3561-3569
9. Couch B.C., and Kohn L.M. A multilocus gene genealogy concordant with host preference indicates segregation of a new species, Magnaporthe oryzae, from M. grisea. Mycologia 94 (2002) 683-693
10. Couch B.C., Fudal I., Lebrun M.H., Tharreau D., Valent B., van Kim P., Notteghem J.L., and Kohn L. Origins of host-specific populations of the blast pathogen, Magnaporthe oryzae, in crop domestication with subsequent expansion of pandemic clones on rice and weeds of rice. Genetics 170 (2005) 613-630
11. Crosthwaite S.K., Loros J.J., and Dunlap J.C. Light-induced resetting of a circadian clock is mediated by a rapid increase in frequency transcript. Cell 81 (1995) 1003-1012
12. De Fabo E.C., Harding R.W., and Shropshire J. Action spectrum between 260 and 800 nanometers for the photoinduction of carotenoid biosynthesis in Neurospora crassa. Plant. Physiol. 57 (1976) 440-445
13. Degli-Innocenti F., and Russo V.E. Isolation of new white collar mutants of Neurospora crassa and studies on their behavior in the blue light-induced formation of protoperithecia. J. Bacteriol. 159 (1984) 757-761
14. Dharmananda, S., 1980. Studies of the circadian clock of Neurospora crassa: light-induced phase shifting. Department of Biology. Santa Cruz, University of California, p. 284.
15. Dunlap J.C., and Loros J.J. The Neurospora circadian system. J. Biol. Rhythms 19 (2004) 414-424
16. Elvin M., Loros J.J., Dunlap J.C., and Heintzen C. The PAS/LOV protein VIVID supports a rapidly dampened daytime oscillator that facilitates entrainment of the Neurospora circadian clock. Genes Dev. 19 (2005) 2593-2605
17. Esser K. Effect of temperature and light on perithecial development in Sordaria macrospora. Mycologia 72 (1980) 619-622
18. Flaherty J.E., and Dunkle L.D. Identification and expression analysis of regulatory genes induced during conidiation in Exserohilum turcicum. Fungal Genet. Biol. 42 (2005) 471-481
19. Franchi L., Fulci V., and Macino G. Protein kinase C modulates light responses in Neurospora by regulating the blue light photoreceptor WC-1. Mol. Microbiol. 56 (2005) 334-345
20. Froehlich A.C., Liu Y., Loros J.J., and Dunlap J.C. White Collar-1, a circadian blue light photoreceptor, binding to the frequency promoter. Science 297 (2002) 815-819
21. Froehlich A.C., Noh B., Vierstra R.D., Loros J., and Dunlap J.C. Genetic and molecular analysis of phytochromes from the filamentous fungus Neurospora crassa. Eukaryot. Cell 4 (2005) 2140-2152
22. Greene A.V., Keller N., Haas H., and Bell-Pedersen D. A circadian oscillator in Aspergillus spp. regulates daily development and gene expression. Eukaryot. Cell 2 (2003) 231-237
23. Harding R.W., and Melles S. Genetic analysis of phototropism of Neurospora crassa perithecial beaks using white collar and albino mutants. Plant. Physiol. 72 (1983) 996-1000
24. Hashioka Y. The microclimate of the paddy field in connection with prevalence of rice blast disease. Agr. Meteorol. Jpn. 6 (1948) 25-59
25. Hashioka, Y., 1963. Effects of environmental factors on development of causal fungus, infection, disease development, and epidemiology in rice blast disease. The International Rice Research Institute, Los Baños, Laguna, Philippines/The Johns Hopkins Press, Baltimore, MD.
26. He Q., Cheng P., Yang Y., Wang L., Gardner K.H., and Liu Y. White Collar-1, a DNA binding transcription factor and a light sensor. Science 297 (2002) 840-843
27. He Q., and Liu Y. Molecular mechanism of light responses in Neurospora: from light-induced transcription to photoadaptation. Genes Dev. 19 (2005) 2888-2899
28. Hill E.P. Effect of light on growth and sporulation of Aspergillus ornatus. J. Gen. Microbiol. 95 (1976) 39-44
29. Honda Y., and Yunoki T. On spectral dependence for maturation of apothecia in Sclerotinia trifoliorum Erik. Ann. Phytopathol. Soc. Jpn. 41 (1975) 383-389
30. Howard R.J., and Valent B. Breaking and entering: host penetration by the fungal rice blast pathogen Magnaporthe grisea. Annu. Rev. Microbiol. 50 (1996) 491-512
31. Idnurm A., and Heitman J. Light controls growth and development via a conserved pathway in the fungal kingdom. PLoS Biol. 3 (2005) e95
32. Imura J. Effects of sunlight on the development of rice blast disease. Ann. Phytopathol. Soc. Jpn. 8 (1938) 23-33
33. Imura J. Effect of sunlight on the incubation periods and development of blast disease and Helminthosporium disease of rice plants. Ann. Phytopathol. Soc. Jpn. 10 (1941) 16-26
34. Ingold C.T. Possible spore discharge mechanism in Pyricularia. Trans. Br. Mycol. Soc. 47 (1964) 573-575
35. Ingold C.T., and Dring V.J. An analysis of spore discharge in Sordaria. Ann. Bot., NS 21 (1957) 465-477
36. Ingold C.T., and Oso B.A. Light and spore discharge in Ascobolus. Ann. Bot., NS 33 (1969) 463-471
37. Innocenti F.D., Pohl U., and Russo V.E.A. Photoinduction of protoperithecia in Neurospora crassa by blue light. Photochem. Photobiol. 37 (1983) 49-51
38. Inoue Y., and Furuya M. Perithecial formation in Gelasinospora reticulispora. III. Inhibitory effects of near-UV and blue light during the inductive dark period. Plant Cell Physiol. 15 (1974) 469-475
39. Inoue Y., and Furuya M. Perithecial formation in Gelasinospora reticulispora. IV. Action spectra for the photoinduction. Plant Physiol. 55 (1975) 1098-1101
40. Inoue Y., and Watanabe M. Perithecial formation in Gelasinospora reticulispora. VII. Action spectra in UV region for the photoinduction and the photoinhibition of photoinductive effect brought on by blue light. Plant Cell Physiol. 25 (1984) 107-113
41. Karniol, B., Wagner, J.R., Walker, J.M., Vierstra, R.D., in press. Phylogenetic analysis of the phytochrome superfamily reveals distinct microbial subfamilies of photoreceptors. Biochem. J. 392, 103-116.
42. Kim C.K., Min H.S., and Yoshino R. Epidemiological studies of rice blast disease caused by Pyricularia oryzae Cavara (III): diurnal pattern of conidial release and dispersal under the natural conditions. Ann. Phytopathol. Soc. Jpn. 56 (1990) 315-321
43. Kues U., and Liu Y. Fruiting body production in Basidiomycetes. Appl. Microbiol. Biotechnol. 54 (2000) 141-152
44. Lauter F.-R., and Russo V.E.A. Blue light induction of conidiation-specific genes in Neurospora crassa. Nucleic Acids Res. 19 (1991) 6883-6886
45. Leach C.M. An action spectrum for light-induced sexual reproduction in the Ascomycete fungus Leptosphaerulina trifolii. Mycologia 64 (1972) 475-490
46. Leung, H., Shi, Z., 1994. Genetic regulation of sporulation in the rice blast fungus. In: Zeigler, R.S., Leong, S.A., Teng, P.S. (Eds.), Rice Blast Disease. CAB International, Oxon, pp. 35-50.
47. Linden H., Ballario P., and Macino G. Blue light regulation in Neurospora crassa. Fungal Genet. Biol. 22 (1997) 141-150
48. Linden H., Rodriguez-Franco M., and Macino G. Mutants of Neurospora crassa defective in regulation of blue light perception. Mol. Gen. Genet. 254 (1997) 111-118
49. Lu Y.K., Sun K.H., and Shen W.C. Blue light negatively regulates the sexual filamentation via the Cwc1 and Cwc2 proteins in Cryptococcus neoformans. Mol. Microbiol. 56 (2005) 480-491
50. Mooney J.L., Hassett D.E., and Yager L.N. Genetic analysis of suppressors of the veA1 mutation in Aspergillus nidulans. Genetics 126 (1990) 869-874
51. Mooney J.L., and Yager L.N. Light is required for conidiation in Aspergillus nidulans. Genes Dev. 4 (1990) 1473-1482
52. Moore-Landecker E. Physiology and biochemistry of ascocarp induction and development. Mycol. Res. 96 (1992) 705-716
53. Moore-Landecker E., and Shropshire Jr. W. Effects of aeration and light on apothecia, sclerotia, and mycelial growth in the discomycete Pyronema domesticum. Mycologia 74 (1982) 1000-1013
54. Ono K., and Suzuki H. Studies on dissemination of conidia of rice blast fungus. Proc. Assoc. Plant Protect. Hokuriku 7 (1959) 6-19
55. Paietta J., and Sargent M.L. Isolation and characterization of light-insensitive mutants of Neurospora crassa. Genetics 104 (1983) 11-21
56. Park S., and Lee K. Inverted race tube assay for circadian clock studies of the Neurospora accessions. Fungal Genet. Newslett. 51 (2004) 12-14
57. Rensing, L., Kallies, A., Gebauer, G., Mohsenzadeh, S., 1995. The effects of temperature change on the circadian clock of Neurospora. [Review]. In: Ciba Foundation Symposium, Vol. 183, pp. 26-41.
58. Rho H.S., Kang S., and Lee Y.H. Agrobacterium tumefaciens-mediated transformation of the plant pathogenic fungus, Magnaporthe grisea. Mol. Cells 12 (2001) 407-411
59. Roenneberg T., and Merrow M. Seasonality and photoperiodism in fungi. J. Biol. Rhythms 16 (2001) 403-414
60. Romani L., Bistoni F., and Puccetti P. Adaptation of Candida albicans to the host environment: the role of morphogenesis in virulence and survival in mammalian hosts. Curr. Opin. Microbiol. 6 (2003) 338-343
61. Sanchez-Murillo R.I., de la Torre-Martinez M., Aguirre-Linares J., and Herrera-Estrella A. Light-regulated asexual reproduction in Paecilomyces fumosoroseus. Microbiology 150 (2004) 311-319
62. Sargent M.L., and Briggs W.R. The effects of light on a circadian rhythm of conidiation in Neurospora. Plant Physiol. 42 (1967) 1504-1510
63. Sargent M.L., and Kaltenborn S.H. Effects of medium composition and carbon dioxide on circadian conidiation in Neurospora. Plant Physiol. 50 (1972) 171-175
64. Sargent M.L., and Woodward D.O. Genetic determinants of circadian rhythmicity in Neurospora. J. Bacteriol. 97 (1969) 867-872
65. Schneper L., Duvel K., and Broach J.R. Sense and sensibility: nutritional response and signal integration in yeast. Curr. Opin. Microbiol. 7 (2004) 624-630
66. Schreckenbach T., Walckhoff B., and Verfuerth C. Blue-light receptor in a white mutant of Physarum polycephalum mediates inhibition of spherulation and regulation of glucose metabolism. Proc. Natl. Acad. Sci. USA 78 (1981) 1009-1013
67. Schwerdtfeger C., and Linden H. Blue light adaptation and desensitization of light signal transduction in Neurospora crassa. Mol. Microbiol. 39 (2001) 1080-1087
68. Schwerdtfeger C., and Linden H. VIVID is a flavoprotein and serves as a fungal blue light photoreceptor for photoadaptation. EMBO J. 22 (2003) 4846-4855
69. Sesma A., and Osbourn A.E. The rice leaf blast pathogen undergoes developmental processes typical of root-infecting fungi. Nature 431 (2004) 582-586
70. Shi Z., Christian D., and Leung H. Interactions between spore morphogenetic mutations affect cell types, sporulation, and pathogenesis in Magnaporthe grisea. Mol. Plant Microbe Interact. 11 (1998) 199-207
71. Shi Z., and Leung H. Genetic analysis and rapid mapping of a sporulation mutation in Magnaporthe grisea. Mol. Plant Microbe Interact. 7 (1994) 113-120
72. Shi Z., and Leung H. Genetic analysis of sporulation in Magnaporthe grisea by chemical and insertional mutagenesis. Mol. Plant Microbe Interact. 8 (1995) 949-959
73. Shrode L.B., Lewis Z.A., White L.D., Bell-Pedersen D., and Ebbole D.J. vvd is required for light adaptation of conidiation-specific genes of Neurospora crassa, but not circadian conidiation. Fungal Genet. Biol. 32 (2001) 169-181
74. Sipiczki M., Takeo K., Yamaguchi M., Yoshida S., and Miklos I. Environmentally controlled dimorphic cycle in a fission yeast. Microbiology 144 Pt 5 (1998) 1319-1330
75. Tan Y., Merrow M., and Roenneberg T. Photoperiodism in Neurospora crassa. J. Biol. Rhythms 19 (2004) 135-143