ライフサイエンスコーパス: Ustilago

1 response element from the sid1 promoter from Ustilago.

2 hown to regulate siderophore biosynthesis in Ustilago.

3 synthase is essential in yeast and that the Ustilago and Trypanosoma synthases are in a different cl

4 fungi, but homologous genes in Magnaporthe, Ustilago, Aspergillus, Fusarium, Epichloe, and Penicilli

5 hment of a new biotrophic model pathosystem: Ustilago bromivora and Brachypodium sp.

6 A gene designated ubc1 (for Ustilago bypass of cyclase) was found to be required for

7 These mutants are named ubc, for Ustilago bypass of cyclase, as they no longer require th

8 s of a uac1 disruption strain, named ubc for Ustilago bypass of cyclase, no longer require cAMP for t

9 persistent infection by a fungal endophyte, Ustilago esculenta.

10 Ustilago hordei is a biotrophic parasite of barley (Hord

11 sa and U. maydis, Sporisorium reilianum, and Ustilago hordei.

12 e same size and specificity as the authentic Ustilago KP4 toxin.

13 -arabinofuranosidases from the basidiomycete Ustilago maydis (UmAbf62A) and ascomycete Podospora anse

14 cell cycle checkpoint protein Rad17 and the Ustilago maydis 3' --> 5' exonuclease, Rec1.

15 tions of ergosterol biosynthesis inhibitors, Ustilago maydis alters the ratio of linoleic to oleic ac

16 eport that an ortholog of DSS1 is present in Ustilago maydis and associates with Brh2, the BRCA2-rela

17 mology to a recombinational repair gene from Ustilago maydis and contain functional domains to hRAD51

18 iring Enzyme1 in the plant pathogenic fungus Ustilago maydis and demonstrate that the UPR is tightly

19 gens such as the phytopathogenic smut fungi, Ustilago maydis and Microbotryum violaceum, must switch

20 as teliospores of the phytopathogenic fungus Ustilago maydis and spores of the social amoeba Dictyost

21 s of the related, maize-infecting smut fungi Ustilago maydis and Sporisorium reilianum but has a larg

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

23 The Basidiomycete fungus Ustilago maydis causes corn smut disease and alternates

24 The biotrophic fungus Ustilago maydis causes smut disease in maize with charac

25 ptides from bovine protein standards, yeast, Ustilago maydis cell lysates, and Arabidopsis thaliana l

26 Mutants of the fungus Ustilago maydis defective in the RecQ helicase Blm are h

27 logenetically closely related plant pathogen Ustilago maydis encodes a different arsenal of extracell

28 The REC2 gene of Ustilago maydis encodes a homologue of the Escherichia c

29 The REC1 gene of Ustilago maydis functions in the maintenance of genome s

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

31 The biotrophic smut fungus Ustilago maydis infects all aerial organs of maize (Zea

32 Ustilago maydis is a biotrophic pathogen causing maize (

33 Ustilago maydis is a dimorphic fungus with a yeast-like

34 Ustilago maydis is a fungal pathogen of maize, some stra

35 Ustilago maydis is a haploid basidiomycete with single g

36 Ustilago maydis is a phytopathogenic fungus exhibiting e

37 Ustilago maydis killer toxins are small polypeptides (7-

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

39 A gene encoding a Ustilago maydis Rad51 orthologue has been isolated, rad5

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

41 Mutation in the REC1 gene of Ustilago maydis results in extreme sensitivity to killin

42 Some strains of the plant-pathogenic fungus Ustilago maydis secrete toxins (killer toxins) that are

43 A small proportion of Ustilago maydis strains produce killer toxins, to which

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

45 verns homologous recombination in the fungus Ustilago maydis through interaction with Rad51.

46 The binding affinity of purified native Ustilago maydis topoisomerase I enzyme for radiolabeled

47 ignated SFU1 that encodes a homologue of the Ustilago maydis URBS1, a transcriptional repressor of si

48 ulosa is related to the model plant pathogen Ustilago maydis yet is not a phytopathogen but rather a

49 Infection of maize by corn smut (Ustilago maydis) provides an agronomically important mod

50 ecific stages of this pathway in maize smut (Ustilago maydis), glucosidase I (Gls1) and glucosidase I

51 n/repair proteins to telomere maintenance in Ustilago maydis, a fungus that bears strong resemblance

52 r DNA repair-defective mutants in the fungus Ustilago maydis, a gene encoding a BRCA2 family member,

53 Ustilago maydis, an edible mushroom growing on maize (Ze

54 One contains the S. cerevisiae, Ustilago maydis, and Trypanosoma brucei enzymes, which h

55 In Ustilago maydis, Aspergillus nidulans, and Saccharomyces

56 s controlling cell fate in the basidiomycete Ustilago maydis, bE5 and bE6, allows cooperative DNA bin

57 and basidiomycetous pathogens and mushrooms (Ustilago maydis, Coprinus cinereus, Schizophyllum commun

58 Brh2, the BRCA2 ortholog in Ustilago maydis, enables recombinational repair of DNA b

59 Brh2, the BRCA2 homolog in Ustilago maydis, functions in recombinational repair of

60 In the elongated hyphal cell of the fungus Ustilago maydis, Higuchi et al. now demonstrate that pol

61 le in the homologous recombination system of Ustilago maydis, mediating delivery of Rad51 to single-s

62 Since the discovery of this process in Ustilago maydis, our understanding of its molecular basi

63 Brh2, the BRCA2 homologue in Ustilago maydis, plays a crucial role in homologous reco

64 Ustilago maydis, the causal agent of corn smut disease,

65 Ustilago maydis, the causal agent of corn smut disease,

66 omosome ends of Saccharomyces cerevisiae and Ustilago maydis, the initial association of helicase gen

67 In the corn smut fungus Ustilago maydis, the myosin-chitin synthase Mcs1 moves t

68 cturally unrelated antifungal toxin KP4 from Ustilago maydis, whereas structurally similar MtDef2 and

69 he ortholog of the BRCA2 tumor suppressor in Ustilago maydis, works hand in hand with Rad51 to promot

70 matical model of early endosome transport in Ustilago maydis.

71 ing plant infection by the pathogenic fungus Ustilago maydis.

72 t early endosome (EE) motility in the fungus Ustilago maydis.

73 chitin synthases (CHSs) in the corn pathogen Ustilago maydis.

74 nthesis from a tryptophan (Trp) precursor in Ustilago maydis.

75 resence of Brh2, the BRCA2 family protein in Ustilago maydis.

76 Rec2 is the single Rad51 paralog in Ustilago maydis.

77 al toxin secreted by the P4 killer strain of Ustilago maydis.

78 A homologues have been identified to date in Ustilago maydis.

79 charomyces cerevisiae, Candida albicans, and Ustilago maydis.

80 al toxin secreted by the P4 killer strain of Ustilago maydis.

81 ein Tsd2 is necessary for DNA replication in Ustilago maydis.

82 meiosis and gene targeting in the corn smut Ustilago maydis.

83 p, a protein required for DNA replication in Ustilago maydis.

84 combinational repair gene from the corn smut Ustilago maydis.

85 for pathogenicity of the corn smut pathogen Ustilago maydis.

86 nal regulator of siderophore biosynthesis in Ustilago maydis.

87 espectively, for siderophore biosynthesis in Ustilago maydis.

88 equired for cell proliferation in the fungus Ustilago maydis.

89 aporthe grisea and the basidiomycete fungus, Ustilago maydis.

90 double-stranded DNA gaps was investigated in Ustilago maydis.

91 tructural and functional similarities of the Ustilago replication-coupled and replication-independent

92 ccinia graminis), and stripe smut (caused by Ustilago striiformis); perennial ryegrass (Lolium perenn

93 idermis and endothecium of Y chromosome- and Ustilago violacea-induced stamens; expression in male an