| heterologous expression can prevent toxic accumulation of ammonium and in return improve dehydration stress tolerance in rice | Over-expression of a glutamate dehydrogenase gene, MgGDH, from Magnaporthe grisea confers tolerance to dehydration stress in transgenic rice.
Zhou Y, Zhang C, Lin J, Yang Y, Peng Y, Tang D, Zhao X, Zhu Y, Liu X. | 02/6/2016 |
| MoCel6A showed higher hydrolytic activities on phosphoric acid-swollen cellulose (PSC), beta-glucan, and cellooligosaccharide derivatives than on cellulose, of which the best substrates were cellooligosaccharides.[MoCel6A] | Characterization of a cellobiohydrolase (MoCel6A) produced by Magnaporthe oryzae.
Takahashi M, Takahashi H, Nakano Y, Konishi T, Terauchi R, Takeda T., Free PMC Article | 01/8/2011 |
| Identified is a PWL2 allele gene, which was termed PWL2D, in a strain of M. grisea. [PWL2] | Overexpression and purification of PWL2D, a mutant of the effector protein PWL2 from Magnaporthe grisea.
Schneider DR, Saraiva AM, Azzoni AR, Miranda HR, de Toledo MA, Pelloso AC, Souza AP. | 12/11/2010 |
| CaM targets to the germ tubes, conidia, mycelia and the least in the aerial hypha. [CaM] | Cloning, prokaryotic expression, and bioactivity of the calmodulin gene of Magnaporthe grisea.
Ma ZB, Zhao JX, Wang LA, Zheng XB. | 01/21/2010 |
| Mstu1 is required for appressorium-mediated infection due to its involvement in the mobilization of lipids and glycogen.[Mstu1] | Mstu1, an APSES transcription factor, is required for appressorium-mediated infection in Magnaporthe grisea.
Nishimura M, Fukada J, Moriwaki A, Fujikawa T, Ohashi M, Hibi T, Hayashi N. | 01/21/2010 |
| The authors conclude that MgCRZ1 is essential for growth, development, and full virulence of Magnaporthe grisea.[CRZ1] | MgCRZ1, a transcription factor of Magnaporthe grisea, controls growth, development and is involved in full virulence.
Zhang H, Zhao Q, Liu K, Zhang Z, Wang Y, Zheng X. | 01/21/2010 |
| PMK1 gene sequence is homologous to MAPK gene. So are their functions. | [Cloning of a homologous gene of Magnaporthe grisea PMK1 type MAPK from Ustilaginoidea virens and functional identification by complement in Magnaporthe grisea corresponding mutant].
Zhang Z, Du X, Chai R, Wang J, Qiu H, Mao X, Sun G. | 01/21/2010 |
| study focuses on expression analysis, recombinant production and biochemical characterization of intracellular catalase/peroxidase of M. grisea (MagKatG1); [MagKatG1] | Intracellular catalase/peroxidase from the phytopathogenic rice blast fungus Magnaporthe grisea: expression analysis and biochemical characterization of the recombinant protein.
Zamocky M, Furtmüller PG, Bellei M, Battistuzzi G, Stadlmann J, Vlasits J, Obinger C. | 01/21/2010 |
| interactions between Rac1 and PAK kinase Chm1 are responsible for conidiogenesis, and between Rac1 and NADPH oxidases Nox1 and Nox2 are important for pathogenicity [Rac1][Chm1] | Rac1 is required for pathogenicity and Chm1-dependent conidiogenesis in rice fungal pathogen Magnaporthe grisea.
Chen J, Zheng W, Zheng S, Zhang D, Sang W, Chen X, Li G, Lu G, Wang Z., Free PMC Article | 01/21/2010 |
| The results demonstrate that MgLig4 is involved in, but not essential for, the non-homologous end-joining system.[MGLIG4 in strain Guy11] | MgLig4, a homolog of Neurospora crassa Mus-53 (DNA ligase IV), is involved in, but not essential for, non-homologous end-joining events in Magnaporthe grisea.
Kito H, Fujikawa T, Moriwaki A, Tomono A, Izawa M, Kamakura T, Ohashi M, Sato H, Abe K, Nishimura M. | 01/21/2010 |
| [ACE1] The avirulence gene ACE1 from the rice blast fungus Magnaporthe grisea encodes a polyketide synthase (PKS) fused to a nonribosomal peptide synthetase (NRPS). | Magnaporthe grisea avirulence gene ACE1 belongs to an infection-specific gene cluster involved in secondary metabolism.
Collemare J, Pianfetti M, Houlle AE, Morin D, Camborde L, Gagey MJ, Barbisan C, Fudal I, Lebrun MH, Böhnert HU. | 01/21/2010 |
| The mig1 deletion mutant had a normal growth rate and formed melanized appressoria, but it was nonpathogenic and failed to infect rice leaves through wounds.[mig1] | MADS-box transcription factor mig1 is required for infectious growth in Magnaporthe grisea.
Mehrabi R, Ding S, Xu JR., Free PMC Article | 01/21/2010 |
| EGL1 endoglucanase from Magnaporthe grisea was characterized [EGL1] | Biochemical and molecular characterization of a putative endoglucanase in Magnaporthe grisea.
Zhou J, Zheng XZ, Lan L, Lin CZ, Wu YB, Lin XJ, Ebbole D, Lu GD, Wang ZH. | 01/21/2010 |
| The data suggests that ABC4 is required for the pathogenicity of M. grisea, helping the fungus to cope with the cytotoxic environment during infection.[ABC4] | Functional analysis of a novel ABC transporter ABC4 from Magnaporthe grisea.
Gupta A, Chattoo BB. | 01/21/2010 |
| Cut2 is therefore required for surface sensing leading to correct germling differentiation, penetration, and full virulence in this model fungus.[Cutinase2] | Magnaporthe grisea cutinase2 mediates appressorium differentiation and host penetration and is required for full virulence.
Skamnioti P, Gurr SJ., Free PMC Article | 01/21/2010 |
| The snodprot1 homolog MSP1 is required for virulence. | The Magnaporthe grisea snodprot1 homolog, MSP1, is required for virulence.
Jeong JS, Mitchell TK, Dean RA. | 01/21/2010 |
| Results describe the involvement of a Magnaporthe grisea serine/threonine kinase gene, MgATG1, in appressorium turgor and pathogenesis [Atg1]. | Involvement of a Magnaporthe grisea serine/threonine kinase gene, MgATG1, in appressorium turgor and pathogenesis.
Liu XH, Lu JP, Zhang L, Dong B, Min H, Lin FC., Free PMC Article | 01/21/2010 |
| MIR1 is an M. grisea-specific gene that is highly conserved among the field isolates belonging to the M. grisea species complex; mir1 mutants had no obvious defects in appressorial penetration and rice infection. [Mir1 gene] | Mirl is highly upregulated and localized to nuclei during infectious hyphal growth in the rice blast fungus.
Li L, Ding SL, Sharon A, Orbach M, Xu JR. | 01/21/2010 |
| Two superoxide-generating NADPH oxidase-encoding genes, Nox1 and Nox2, are independently required for pathogenicity of M. grisea. [Nox1 & Nox2 NADPH oxidase] | Generation of reactive oxygen species by fungal NADPH oxidases is required for rice blast disease.
Egan MJ, Wang ZY, Jones MA, Smirnoff N, Talbot NJ., Free PMC Article | 01/21/2010 |
| These data indicate that the MAPK-docking site of Mst7 is essential for its association and activation of downstream Pmk1, and the Mst7-Pmk1 interaction is enhanced or stabilized during appressorium formation. [Mst7, Pmk1] | A highly conserved MAPK-docking site in Mst7 is essential for Pmk1 activation in Magnaporthe grisea.
Zhao X, Xu JR. | 01/21/2010 |
| These observations suggest that Con7p encodes a transcription factor required for the transcription of several genes which participate in disease-related morphogenesis in M. grisea.[Con7p] | The transcription factor Con7p is a central regulator of infection-related morphogenesis in the rice blast fungus Magnaporthe grisea.
Odenbach D, Breth B, Thines E, Weber RW, Anke H, Foster AJ. | 01/21/2010 |
| These experiments suggest that ACE1 appressorium-specific expression does not depend on host plant signals but is connected to the onset of appressorium-mediated penetration. [ACE1 protein] | Expression of Magnaporthe grisea avirulence gene ACE1 is connected to the initiation of appressorium-mediated penetration.
Fudal I, Collemare J, Böhnert HU, Melayah D, Lebrun MH., Free PMC Article | 01/21/2010 |
| Rgs1 regulates multiple Galpha subunits in Magnaporthe pathogenesis, asexual growth and thigmotropism. [Rgs1] | Rgs1 regulates multiple Galpha subunits in Magnaporthe pathogenesis, asexual growth and thigmotropism.
Liu H, Suresh A, Willard FS, Siderovski DP, Lu S, Naqvi NI., Free PMC Article | 01/21/2010 |