Literature DB >> 8914511

Green fluorescent protein (GFP) as a new vital marker in the phytopathogenic fungus Ustilago maydis.

T Spellig1, A Bottin, R Kahmann.   

Abstract

Pathogenic development of Ustilago maydis, the causative agent of corn smut disease, is a multistep process. Compatible yeast-like cells fuse and this generates the infectious dikaryon which grows filamentously. Having entered the plant the dikaryon induces tumors in its host in which massive proliferation of fungal material, karyogamy and spore formation occur. In order to follow fungal development from the initial steps to the final stage we have expressed the green fluorescent protein (GFP) from Aequorea victoria as a vital marker in U. maydis and demonstrate that GFP-tagged strains can be used to study host-pathogen interactions in vivo.

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Year:  1996        PMID: 8914511     DOI: 10.1007/bf02172396

Source DB:  PubMed          Journal:  Mol Gen Genet        ISSN: 0026-8925


  25 in total

Review 1.  Ustilago maydis, the delightful blight.

Authors:  F Banuett
Journal:  Trends Genet       Date:  1992-05       Impact factor: 11.639

2.  The a mating type locus of U. maydis specifies cell signaling components.

Authors:  M Bölker; M Urban; R Kahmann
Journal:  Cell       Date:  1992-02-07       Impact factor: 41.582

3.  The b alleles of U. maydis, whose combinations program pathogenic development, code for polypeptides containing a homeodomain-related motif.

Authors:  B Schulz; F Banuett; M Dahl; R Schlesinger; W Schäfer; T Martin; I Herskowitz; R Kahmann
Journal:  Cell       Date:  1990-01-26       Impact factor: 41.582

4.  GFP in plants.

Authors:  J Haseloff; B Amos
Journal:  Trends Genet       Date:  1995-08       Impact factor: 11.639

5.  Green fluorescent protein as a marker for gene expression.

Authors:  M Chalfie; Y Tu; G Euskirchen; W W Ward; D C Prasher
Journal:  Science       Date:  1994-02-11       Impact factor: 47.728

6.  Different a alleles of Ustilago maydis are necessary for maintenance of filamentous growth but not for meiosis.

Authors:  F Banuett; I Herskowitz
Journal:  Proc Natl Acad Sci U S A       Date:  1989-08       Impact factor: 11.205

7.  Primary structure of the Aequorea victoria green-fluorescent protein.

Authors:  D C Prasher; V K Eckenrode; W W Ward; F G Prendergast; M J Cormier
Journal:  Gene       Date:  1992-02-15       Impact factor: 3.688

8.  Pathways of transformation in Ustilago maydis determined by DNA conformation.

Authors:  S Fotheringham; W K Holloman
Journal:  Genetics       Date:  1990-04       Impact factor: 4.562

9.  Implications for bcd mRNA localization from spatial distribution of exu protein in Drosophila oogenesis.

Authors:  S Wang; T Hazelrigg
Journal:  Nature       Date:  1994-06-02       Impact factor: 49.962

10.  Mutation in a heat-regulated hsp70 gene of Ustilago maydis.

Authors:  D W Holden; J W Kronstad; S A Leong
Journal:  EMBO J       Date:  1989-07       Impact factor: 11.598

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  86 in total

Review 1.  Green fluorescent protein is lighting up fungal biology.

Authors:  J M Lorang; R P Tuori; J P Martinez; T L Sawyer; R S Redman; J A Rollins; T J Wolpert; K B Johnson; R J Rodriguez; M B Dickman; L M Ciuffetti
Journal:  Appl Environ Microbiol       Date:  2001-05       Impact factor: 4.792

2.  Concentration of antifungal agents within host cell membranes: a new paradigm governing the efficacy of prophylaxis.

Authors:  P Campoli; Q Al Abdallah; R Robitaille; N V Solis; J A Fielhaber; A S Kristof; M Laverdiere; S G Filler; D C Sheppard
Journal:  Antimicrob Agents Chemother       Date:  2011-09-19       Impact factor: 5.191

3.  Immunolocalization of dinitrogenase reductase produced by Klebsiella pneumoniae in association with Zea mays L.

Authors:  M K Chelius; E W Triplett
Journal:  Appl Environ Microbiol       Date:  2000-02       Impact factor: 4.792

4.  Cotransformation of Trichoderma harzianum with beta-glucuronidase and green fluorescent protein genes provides a useful tool for monitoring fungal growth and activity in natural soils.

Authors:  Y S Bae; G R Knudsen
Journal:  Appl Environ Microbiol       Date:  2000-02       Impact factor: 4.792

5.  Mating and pathogenic development of the Smut fungus Ustilago maydis are regulated by one mitogen-activated protein kinase cascade.

Authors:  Philip Müller; Gerhard Weinzierl; Andreas Brachmann; Michael Feldbrügge; Regine Kahmann
Journal:  Eukaryot Cell       Date:  2003-12

6.  Identification of plant-regulated genes in Ustilago maydis by enhancer-trapping mutagenesis.

Authors:  C Aichinger; K Hansson; H Eichhorn; F Lessing; G Mannhaupt; W Mewes; R Kahmann
Journal:  Mol Genet Genomics       Date:  2003-10-02       Impact factor: 3.291

7.  PKA and MAPK phosphorylation of Prf1 allows promoter discrimination in Ustilago maydis.

Authors:  Florian Kaffarnik; Philip Müller; Marc Leibundgut; Regine Kahmann; Michael Feldbrügge
Journal:  EMBO J       Date:  2003-11-03       Impact factor: 11.598

8.  A reverse genetic approach for generating gene replacement mutants in Ustilago maydis.

Authors:  A Brachmann; J König; C Julius; M Feldbrügge
Journal:  Mol Genet Genomics       Date:  2004-08-17       Impact factor: 3.291

9.  Coordination of cytokinesis and cell separation by endosomal targeting of a Cdc42-specific guanine nucleotide exchange factor in Ustilago maydis.

Authors:  Kay Oliver Schink; Michael Bölker
Journal:  Mol Biol Cell       Date:  2008-12-10       Impact factor: 4.138

10.  A H2O2-producing glyoxal oxidase is required for filamentous growth and pathogenicity in Ustilago maydis.

Authors:  B Leuthner; C Aichinger; E Oehmen; E Koopmann; O Müller; P Müller; R Kahmann; M Bölker; P H Schreier
Journal:  Mol Genet Genomics       Date:  2004-12-01       Impact factor: 3.291

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