Valent B, Chumley FG. Molecular genetic analysis of the rice blast fungus Magnaporthe grisea. Annu Rev Phytopathol. 1991;29:443–67.
Talbot NJ. On the trail of a cereal killer: Exploring the biology of Magnaporthe grisea. Annu Rev Microbiol. 2003;57:177–202.
Howard RJ, Ferrari MA, Roach DH, Money NP. Penetration of hard substrates by a fungus employing enormous turgor pressures. Proc Natl Acad Sci USA. 1991;88(24):11281–4.
de Jong JC, McCormack BJ, Smirnoff N, Talbot NJ. Glycerol generates turgor in rice blast. Nature. 1997;389(6648):244–5.
Pabo CO, Sauer RT. Transcription factors: structural families and principles of DNA recognition. Annu Rev Biochem. 1992;61:1053–95.
Li G, Zhou X, Xu JR. Genetic control of infection-related development in Magnaporthe oryzae. Curr Opin Microbiol. 2012;15(6):678–84.
Kim S, Park S-Y, Kim KS, Rho H-S, Chi M-H, Choi J, et al. Homeobox transcription factors are required for conidiation and appressorium development in the rice blast fungus Magnaporthe oryzae. PLoS Genet. 2009;5(12):e1000757.
Zhang H, Zhao Q, Liu K, Zhang Z, Wang Y, Zheng X. MgCRZ1, a transcription factor of Magnaporthe grisea, controls growth, development and is involved in full virulence. FEMS Microbiol Lett. 2009;293(2):160–9.
Guo M, Chen Y, Du Y, Dong Y, Guo W, Zhai S, et al. The bZIP transcription factor MoAP1 mediates the oxidative stress response and is critical for pathogenicity of the rice blast fungus Magnaporthe oryzae. PLoS Pathog. 2011;7(2):e1001302.
Qi Z, Wang Q, Dou X, Wang W, Zhao Q, Lv R, et al. MoSwi6, an APSES family transcription factor, interacts with MoMps1 and is required for hyphal and conidial morphogenesis, appressorial function and pathogenicity of Magnaporthe oryzae. Mol Plant Pathol. 2012;13(7):677–89.
Zhang H, Zhao Q, Guo X, Guo M, Qi Z, Tang W, et al. Pleiotropic function of the putative zinc-finger protein MoMsn2 in Magnaporthe oryzae. Mol Plant Microbe Interact. 2014;27:446–60.
Guo M, Guo W, Chen Y, Dong S, Zhang X, Zhang H, et al. The basic leucine zipper transcription factor Moatf1 mediates oxidative stress responses and is necessary for full virulence of the rice blast fungus Magnaporthe oryzae. Mol Plant Microbe Interact. 2010;23(8):1053–68.
Tang W, Ru Y, Hong L, Zhu Q, Zuo R, Guo X, et al. System-wide characterization of bZIP transcription factor proteins involved in infection-related morphogenesis of Magnaporthe oryzae. Environ Microbiol 2014. doi:10.1111/1462-2920.12618
Stracke R, Werber M, Weisshaar B. The R2R3-MYB gene family in Arabidopsis thaliana. Curr Opin Plant Biol. 2001;4(5):447–56.
Klempnauer KH, Gonda TJ, Bishop JM. Nucleotide sequence of the retroviral leukemia gene v-myb and its cellular progenitor c-myb: the architecture of a transduced oncogene. Cell. 1982;31(2 Pt 1):453–63.
Jin H, Martin C. Multifunctionality and diversity within the plant MYB-gene family. Plant Mol Biol. 1999;41(5):577–85.
Thompson MA, Ramsay RG. Myb: an old oncoprotein with new roles. Bioessays. 1995;17(4):341–50.
Rosinski JA, Atchley WR. Molecular evolution of the Myb family of transcription factors: evidence for polyphyletic origin. J Mol Evol. 1998;46(1):74–83.
Weston K. Myb proteins in life, death and differentiation. Curr Opin Genet Dev. 1998;8(1):76–81.
Ito M. Conservation and diversification of three-repeat Myb transcription factors in plants. J Plant Res. 2005;118(1):61–9.
Martin C, PazAres J. MYB transcription factors in plants. Trends Genet. 1997;13(2):67–73.
Ohi R, McCollum D, Hirani B, Den Haese GJ, Zhang X, Burke JD, et al. The Schizosaccharomyces pombe cdc5+ gene encodes an essential protein with homology to c-Myb. EMBO J. 1994;13(2):471–83.
Wieser J, Adams TH. flbD encodes a Myb-like DNA-binding protein that coordinates initiation of Aspergillus nidulans conidiophore development. Genes Dev. 1995;9(4):491–502.
Ohi R, Feoktistova A, McCann S, Valentine V, Look AT, Lipsick JS, et al. Myb-related Schizosaccharomyces pombe cdc5p is structurally and functionally conserved in eukaryotes. Mol Cell Biol. 1998;18(7):4097–108.
Talbot NJ, Ebbole DJ, Hamer JE. ldentification and characterization of MPGI, a gene involved in pathogenicity from the rice blast fungus Magnaporthe grisea. Plant Cell. 1993;5:1575–90.
Zhang H, Liu K, Zhang X, Song W, Zhao Q, Dong Y, et al. A two-component histidine kinase, MoSLN1, is required for cell wall integrity and pathogenicity of the rice blast fungus. Magnaporthe oryzae. Curr Genet. 2010;56(6):517–28.
Zhang H, Liu K, Zhang X, Tang W, Wang J, Guo M, et al. Two phosphodiesterase genes, PDEL and PDEH, regulate development and pathogenicity by modulating intracellular cyclic AMP levels in Magnaporthe oryzae. PLoS One. 2011;6(2):e17241.
Bruno KS, Tenjo F, Li L, Hamer JE, Xu J-R. Cellular localization and role of kinase activity of PMK1 in Magnaporthe grisea. Eukaryot Cell. 2004;3(6):1525–32.
Dufresne M, Osbourn AE. Definition of tissue-specific and general requirements for plant infection in a phytopathogenic fungus. Mol Plant-Microbe Interact. 2001;14(3):300–7.
Chen Y, Zhai S, Zhang H, Zuo R, Wang J, Guo M, et al. Shared and distinct functions of two Gti1/Pac2 family proteins in growth, morphogenesis and pathogenicity of Magnaporthe oryzae. Environ Microbiol. 2014;16(3):788–801.
Bulik DA, Olczak M, Lucero HA, Osmond BC, Robbins PW, Specht CA. Chitin synthesis in Saccharomyces cerevisiae in response to supplementation of growth medium with glucosamine and cell wall stress. Eukaryot Cell. 2003;2(5):886–900.
Song W, Dou X, Qi Z, Wang Q, Zhang X, Zhang H, et al. R-SNARE homolog MoSec22 is required for conidiogenesis, cell wall integrity, and pathogenesis of Magnaporthe oryzae. PloS One. 2010;5(10):e13193.
Jeon J, Goh J, Yoo S, Chi M-H, Choi J, Rho H-S, et al. A putative MAP kinase kinase kinase, MCK1, is required for cell wall integrity and pathogenicity of the rice blast fungus. Magnaporthe oryzae. Mol Plant-Microbe Interact. 2008;21(5):525–34.
Dou X, Wang Q, Qi Z, Song W, Wang W, Guo M, et al. MoVam7, a conserved SNARE involved in vacuole assembly, is required for growth, endocytosis, ROS accumulation, and pathogenesis of Magnaporthe oryzae. PloS One. 2011;6(1):e16439.
Sambrook J, Fritsch EF, Maniatis T. Molecular Cloning: a Laboratory Manual. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press; 1989.
Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2(T)(−Delta Delta C) method. Methods. 2001;25(4):402–8.
Dean RA, Talbot NJ, Ebbole DJ, Farman ML, Mitchell TK, Orbach MJ, et al. The genome sequence of the rice blast fungus Magnaporthe grisea. Nature. 2005;434:989–6.
McGinnis S, Madden TL. BLAST: at the core of a powerful and diverse set of sequence analysis tools. Nucleic Acids Res. 2004;32(Web Server issue):W20–5.
Thompson JD, Higgins DG, Gibson TJ. CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res. 1994;22(22):4673–80.
Aasland R, Stewart AF, Gibson T. The SANT domain: A putative DNA-binding domain in the SWI-SNF and ADA complexes, the transcriptional corepressor N-CoR and TFIIIB. Trends Biochem Sci. 1996;21(3):87–8.
Majello B, Kenyon LC, Dalla-Favera R. Human c-myb protooncogene: nucleotide sequence of cDNA and organization of the genomic locus. Proc Natl Acad Sci USA. 1986;83(24):9636–40.
Slamon DJ, Boone TC, Murdock DC, Keith DE, Press MF, Larson RA, et al. Studies of the human c-myb gene and its product in human acute leukemias. Science. 1986;233(4761):347–51.
Bender J, Fink GR. A Myb homologue, ATR1, activates tryptophan gene expression in Arabidopsis. Proc Natl Acad Sci USA. 1998;95(10):5655–60.
Paz-Ares J, Ghosal D, Wienand U, Peterson PA, Saedler H. The regulatory c1 locus of Zea mays encodes a protein with homology to myb proto-oncogene products and with structural similarities to transcriptional activators. EMBO J. 1987;6(12):3553–8.
Tice-Baldwin K, Fink GR, Arndt KT. BAS1 has a Myb motif and activates HIS4 transcription only in combination with BAS2. Science. 1989;246(4932):931–5.
Zhou Z, Li G, Lin C, He C. Conidiophore stalk-less1 encodes a putative zinc-finger protein involved in the early stage of conidiation and mycelial infection in Magnaporthe oryzae. Mol Plant-Microbe Interact. 2009;22(4):402–10.
Kong L, Yang J, Li G, Qi L, Zhang Y, Wang C, et al. Different chitin synthase genes are required for various developmental and plant infection processes in the rice blast fungus Magnaporthe oryzae. PLoS Pathog. 2012;8(2):e1002526.
Tucker SL, Besi MI, Galhano R, Franceschetti M, Goetz S, Lenhert S, et al. Common genetic pathways regulate organ-specific infection-related development in the rice blast fungus. Plant Cell. 2010;22(3):953–72.
Larkin JC, Oppenheimer DG, Lloyd AM, Paparozzi ET, Marks MD. Roles of the glabrous1 and transparent testa glabra genes in Arabidopsis trichome Development. Plant Cell. 1994;6(8):1065–76.
Soulie MC, Piffeteau A, Choquer M, Boccara M, Vidal-Cros A. Disruption of Botrytis cinerea class I chitin synthase gene Bcchs1 results in cell wall weakening and reduced virulence. Fungal Genet Biol. 2003;40(1):38–46.
Soulie MC, Perino C, Piffeteau A, Choquer M, Malfatti P, Cimerman A, et al. Botrytis cinerea virulence is drastically reduced after disruption of chitin synthase class III gene (Bcchs3a). Cell Microbiol. 2006;8(8):1310–21.
Madrid MP, Di Pietro A, Roncero MIG. Class V chitin synthase determines pathogenesis in the vascular wilt fungus Fusarium oxysporum and mediates resistance to plant defence compounds. Mol Microbiol. 2003;47(1):257–66.
Martin-Udiroz M, Madrid MP, Roncero MIG. Role of chitin synthase genes in Fusarium oxysporum. Microbiol-Sgm. 2004;150:3175–87.
Odenbach D, Thines E, Anke H, Foster AJ. The Magnaporthe grisea class VII chitin synthase is required for normal appressorial development and function. Mol Plant Pathol. 2009;10(1):81–94.