Literature DB >> 3065450

A complementation analysis by parasexual recombination of Candida albicans morphological mutants.

C Gil1, R Pomés, C Nombela.   

Abstract

Benomyl treatment (at 100 micrograms ml-1) of Candida albicans 1001, and other strains derived from it, determined the appearance of morphological mutants similar to those derived from UV irradiation treatment. A permanent alteration in the morphogenesis of these mutant strains determined their inability to grow by budding, to form oval yeast cells or blastospores (Y-phenotype) and their growth as long filamentous forms, mostly with the appearance of pseudomycelium, giving rise to rough colonies (R phenotype). In order to carry out a genetic complementation analysis, we isolated morphological mutants that carried other genetic markers (nutritional, conditional lethal) adequate for crosses by means of protoplast fusion. Wild-type hybrids of regular mononuclear oval yeast cells and smooth colonies were obtained by crossing pairs of complementing mutants, whereas hybrids from crosses of non-complementing mutants still retained their morphological alterations. Our results define two complementation groups, which represent two genes relevant for dimorphism, whose alteration interferes with the correct transition from blastospores to mycelium.

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Year:  1988        PMID: 3065450     DOI: 10.1099/00221287-134-6-1587

Source DB:  PubMed          Journal:  J Gen Microbiol        ISSN: 0022-1287


  10 in total

1.  The histone deacetylase genes HDA1 and RPD3 play distinct roles in regulation of high-frequency phenotypic switching in Candida albicans.

Authors:  T Srikantha; L Tsai; K Daniels; A J Klar; D R Soll
Journal:  J Bacteriol       Date:  2001-08       Impact factor: 3.490

2.  Characterization of Candida albicans colony-morphology mutants and their hybrids.

Authors:  A Novák; C Vágvölgyi; M Pesti
Journal:  Folia Microbiol (Praha)       Date:  2003       Impact factor: 2.099

3.  Characterization of Candida albicans colony morphological mutants and their hybrids by means of RAPD-PCR, isoenzyme analysis and pathogenicity analysis.

Authors:  A Novák; C Vágvölgyi; L Emody; M Pesti
Journal:  Folia Microbiol (Praha)       Date:  2004       Impact factor: 2.099

Review 4.  High-frequency switching in Candida albicans.

Authors:  D R Soll
Journal:  Clin Microbiol Rev       Date:  1992-04       Impact factor: 26.132

Review 5.  Genetics of Candida albicans.

Authors:  S Scherer; P T Magee
Journal:  Microbiol Rev       Date:  1990-09

6.  Large-scale identification of putative exported proteins in Candida albicans by genetic selection.

Authors:  L Monteoliva; M López Matas; C Gil; C Nombela; J Pla
Journal:  Eukaryot Cell       Date:  2002-08

7.  Isolation and characterization of Candida albicans morphological mutants derepressed for the formation of filamentous hypha-type structures.

Authors:  C Gil; R Pomés; C Nombela
Journal:  J Bacteriol       Date:  1990-05       Impact factor: 3.490

8.  Elevated phenotypic switching and drug resistance of Candida albicans from human immunodeficiency virus-positive individuals prior to first thrush episode.

Authors:  K Vargas; S A Messer; M Pfaller; S R Lockhart; J T Stapleton; J Hellstein; D R Soll
Journal:  J Clin Microbiol       Date:  2000-10       Impact factor: 5.948

9.  Induced chromosome rearrangements and morphologic variation in Candida albicans.

Authors:  R C Barton; S Scherer
Journal:  J Bacteriol       Date:  1994-02       Impact factor: 3.490

10.  Functional characterization of the MKC1 gene of Candida albicans, which encodes a mitogen-activated protein kinase homolog related to cell integrity.

Authors:  F Navarro-García; M Sánchez; J Pla; C Nombela
Journal:  Mol Cell Biol       Date:  1995-04       Impact factor: 4.272

  10 in total

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