ライフサイエンスコーパス: maydis

1 rol of morphogenesis and pathogenicity in U. maydis.

2 is necessary for DNA replication in Ustilago maydis.

3 and gene targeting in the corn smut Ustilago maydis.

4 ein required for DNA replication in Ustilago maydis.

5 onal repair gene from the corn smut Ustilago maydis.

6 ogenicity of the corn smut pathogen Ustilago maydis.

7 ator of siderophore biosynthesis in Ustilago maydis.

8 ly, for siderophore biosynthesis in Ustilago maydis.

9 or cell proliferation in the fungus Ustilago maydis.

10 risea and the basidiomycete fungus, Ustilago maydis.

11 randed DNA gaps was investigated in Ustilago maydis.

12 odel of early endosome transport in Ustilago maydis.

13 infection by the pathogenic fungus Ustilago maydis.

14 ndosome (EE) motility in the fungus Ustilago maydis.

15 raction of maize with the fungal pathogen U. maydis.

16 nthases (CHSs) in the corn pathogen Ustilago maydis.

17 icient homologous recombination system in U. maydis.

18 rom a tryptophan (Trp) precursor in Ustilago maydis.

19 f Brh2, the BRCA2 family protein in Ustilago maydis.

20 getative and sporulating cultures of C. zeae-maydis.

21 s for the extreme radiation resistance in U. maydis.

22 Rec2 is the single Rad51 paralog in Ustilago maydis.

23 s cerevisiae, Candida albicans, and Ustilago maydis.

24 secreted by the P4 killer strain of Ustilago maydis.

25 ues have been identified to date in Ustilago maydis.

26 ichrome and ferrichrome A biosynthesis in U. maydis.

27 nstrate that KP4 affects (45)Ca uptake in U. maydis.

28 heromone-responsive MAP kinase cascade in U. maydis.

29 secreted by the P4 killer strain of Ustilago maydis.

30 f filamentous growth and pathogenicity in U. maydis.

31 le checkpoint protein Rad17 and the Ustilago maydis 3' --> 5' exonuclease, Rec1.

32 proteins to telomere maintenance in Ustilago maydis, a fungus that bears strong resemblance to mammal

33 air-defective mutants in the fungus Ustilago maydis, a gene encoding a BRCA2 family member, designate

34 ergosterol biosynthesis inhibitors, Ustilago maydis alters the ratio of linoleic to oleic acid bound

35 Ustilago maydis, an edible mushroom growing on maize (Zea mays),

36 Studies in U. maydis and Aspergillus nidulans reveal a complex interpl

37 t an ortholog of DSS1 is present in Ustilago maydis and associates with Brh2, the BRCA2-related prote

38 a recombinational repair gene from Ustilago maydis and contain functional domains to hRAD51 and hLIM

39 yme1 in the plant pathogenic fungus Ustilago maydis and demonstrate that the UPR is tightly interlink

40 expressed sequence tags (ESTs) from C. zeae-maydis and evaluate their expression during vegetative,

41 as the phytopathogenic smut fungi, Ustilago maydis and Microbotryum violaceum, must switch from a ye

42 The two genes from U. maydis and one of the genes from M. violaceum were expre

43 pores of the phytopathogenic fungus Ustilago maydis and spores of the social amoeba Dictyostelium dis

44 related, maize-infecting smut fungi Ustilago maydis and Sporisorium reilianum but has a larger repeat

45 ora sorghi in cluster I, five isolates of P. maydis and three isolates of P. sacchari in cluster II a

46 in the recombinational repair pathway in U. maydis, and imply that it plays a similar key role in th

47 One contains the S. cerevisiae, Ustilago maydis, and Trypanosoma brucei enzymes, which have a COO

48 Here we show that in the fungus Ustilago maydis approximately 95% of POs and LDs undergo diffusiv

49 oteins reported to influence virulence in U. maydis as the singular divergence that could explain its

50 In Ustilago maydis, Aspergillus nidulans, and Saccharomyces cerevisi

51 ut the regulation of pathogenesis in C. zeae-maydis at the molecular level.

52 5 transformants/micrograms linear DNA and U. maydis at up to 25 transformants/microgram circular DNA

53 ling cell fate in the basidiomycete Ustilago maydis, bE5 and bE6, allows cooperative DNA binding with

54 ized for Bipolaris zeicola and Stenocarpella maydis, but the identities of the proteases are not know

55 The Basidiomycete fungus Ustilago maydis causes corn smut disease and alternates between a

56 The biotrophic fungus Ustilago maydis causes smut disease in maize with characteristic

57 om bovine protein standards, yeast, Ustilago maydis cell lysates, and Arabidopsis thaliana leaves.

58 Here, we show that the U. maydis class VII chitin synthase and 1,3-beta-glucan syn

59 iomycetous pathogens and mushrooms (Ustilago maydis, Coprinus cinereus, Schizophyllum commune), yet o

60 Mutants of the fungus Ustilago maydis defective in the RecQ helicase Blm are highly sen

61 Mutants of U. maydis deleted of DSS1 are extremely radiation sensitive

62 In telomerase-positive U. maydis, deletion of rad51 and blm separately caused shor

63 While U. maydis Deltagls1 cells induce strong plant defense respo

64 U. maydis deploys many effector proteins to manipulate its

65 For U. maydis, disruption of ump2 eliminated the filamentous ph

66 9 is not induced after infection with the U. maydis effector mutant Deltapep1, which elicits massive

67 Brh2, the BRCA2 ortholog in Ustilago maydis, enables recombinational repair of DNA by control

68 ally closely related plant pathogen Ustilago maydis encodes a different arsenal of extracellular hydr

69 The REC2 gene of Ustilago maydis encodes a homologue of the Escherichia coli RecA

70 The REC1 gene of Ustilago maydis functions in the maintenance of genome stability

71 Brh2, the BRCA2 homolog in Ustilago maydis, functions in recombinational repair of DNA damag

72 is evident by blast analysis of the Ustilago maydis genome database.

73 n genome defense, that are lacking in the U. maydis genome due to clean excision events.

74 ages of this pathway in maize smut (Ustilago maydis), glucosidase I (Gls1) and glucosidase II beta-su

75 The unusual C-terminal extension of the U. maydis Hac1 homolog, Cib1 (for Clp1 interacting bZIP1),

76 elongated hyphal cell of the fungus Ustilago maydis, Higuchi et al. now demonstrate that polysomes as

77 firm and extend earlier observations that U. maydis hyphae branch extensively on the leaf surface and

78 lignin biosynthesis are hypersensitive to U. maydis infection.

79 The biotrophic smut fungus Ustilago maydis infects all aerial organs of maize (Zea mays) and

80 Ustilago maydis is a biotrophic pathogen causing maize (Zea mays)

81 Ustilago maydis is a dimorphic fungus with a yeast-like non-patho

82 Ustilago maydis is a fungal pathogen of maize, some strains of wh

83 Ustilago maydis is a haploid basidiomycete with single genes for

84 Ustilago maydis is a phytopathogenic fungus exhibiting extreme re

85 The ascomycete fungus Cercospora zeae-maydis is an aggressive foliar pathogen of maize that ca

86 These results indicate that gap repair in U. maydis is unlikely to proceed by the mechanism envisione

87 The U. maydis killer toxin KP6 contains two polypeptide chains,

88 Ustilago maydis killer toxins are small polypeptides (7-14 kDa) w

89 three well-characterized killer toxins in U. maydis-KP1, KP4, and KP6-which are secreted by the P1, P

90 slocation of a number of effectors in the U. maydis-maize system and show data that suggest that the

91 homologous recombination system of Ustilago maydis, mediating delivery of Rad51 to single-stranded D

92 NPC motility required F-actin, whereas in U. maydis, microtubules, kinesin-1, and dynein drove pore m

93 henotypes mirror previous observations of U. maydis mutants deficient in Brh2 or Rad51.

94 Phenotypic screening of U. maydis mutants deleted for genes encoding secreted prote

95 In S. cerevisiae and U. maydis, NPC motility prevented NPCs from clustering.

96 Recapitulation in U. maydis of defects in DNA repair and genome stability ass

97 Brh2 is the Ustilago maydis ortholog of the BRCA2 tumor suppressor.

98 ce the discovery of this process in Ustilago maydis, our understanding of its molecular basis and bio

99 DNA from downy mildews that attack maize (P. maydis & P. philippinensis), sugar cane (P. sacchari), p

100 Brh2, the BRCA2 homologue in Ustilago maydis, plays a crucial role in homologous recombination

101 Infection of maize by corn smut (Ustilago maydis) provides an agronomically important model of bio

102 and pathogenesis were identified in C. zeae-maydis, providing specific targets for characterization

103 A gene encoding a Ustilago maydis Rad51 orthologue has been isolated, rad51-1, a mu

104 ces pombe rad1+ gene product and to Ustilago maydis Rec1, a known 3'->5'exonuclease.

105 A repair and recombination proficiency in U. maydis requires both Rec2 and Rad51.

106 Mutation in the REC1 gene of Ustilago maydis results in extreme sensitivity to killing by ultr

107 ains of the plant-pathogenic fungus Ustilago maydis secrete toxins (killer toxins) that are lethal to

108 oter and iron-regulatory sequences of the U. maydis sid1 gene were defined by fusing restriction and

109 ty, are very similar in P. flocculosa and U. maydis, Sporisorium reilianum, and Ustilago hordei.

110 A small proportion of Ustilago maydis strains produce killer toxins, to which they are

111 maize plants and on engineering of Ustilago maydis strains to secrete Avitagged effectors.

112 double-stranded RNA (dsRNA) virus in each U. maydis subtype.

113 Ustilago maydis, the causal agent of corn smut disease, acquires

114 Ustilago maydis, the causal agent of corn smut disease, displays

115 nds of Saccharomyces cerevisiae and Ustilago maydis, the initial association of helicase genes with f

116 In the corn smut fungus Ustilago maydis, the myosin-chitin synthase Mcs1 moves to the pla

117 ologous recombination in the fungus Ustilago maydis through interaction with Rad51.

118 binding affinity of purified native Ustilago maydis topoisomerase I enzyme for radiolabeled DNA subst

119 uranosidases from the basidiomycete Ustilago maydis (UmAbf62A) and ascomycete Podospora anserina (PaA

120 Moreover, the U. maydis ump2 gene, initially detected as an upregulated g

121 tion of a system enabling the survival of U. maydis under such conditions could be a secondary conseq

122 Our findings suggest that in U. maydis, unprotected telomeres arising from Ku depletion

123 FU1 that encodes a homologue of the Ustilago maydis URBS1, a transcriptional repressor of siderophore

124 unrelated antifungal toxin KP4 from Ustilago maydis, whereas structurally similar MtDef2 and the radi

125 atin (CC9) is induced upon penetration by U. maydis wild type.

126 pression and a hypersensitive response to U. maydis wild-type infection.

127 og of the BRCA2 tumor suppressor in Ustilago maydis, works hand in hand with Rad51 to promote repair

128 related to the model plant pathogen Ustilago maydis yet is not a phytopathogen but rather a biocontro