Literature DB >> 8550405

The sea pansy Renilla reniformis luciferase serves as a sensitive bioluminescent reporter for differential gene expression in Candida albicans.

T Srikantha1, A Klapach, W W Lorenz, L K Tsai, L A Laughlin, J A Gorman, D R Soll.   

Abstract

The infectious yeast Candida albicans progresses through two developmental programs which involve differential gene expression, the bud-hypha transition and high-frequency phenotypic switching. To understand how differentially expressed genes are regulated in this organism, the promoters of phase-specific genes must be functionally characterized, and a bioluminescent reporter system would facilitate such characterization. However, C. albicans has adopted a nontraditional codon strategy that involves a tRNA with a CAG anticodon to decode the codon CUG as serine rather than leucine. Since the luciferase gene of the sea pansy Renilla reinformis contains no CUGs, we have used it to develop a highly sensitive bioluminescent reporter system for C. albicans. When fused to the galactose-inducible promoter of GAL1, luciferase activity is inducible; when fused to the constitutive EF1 alpha 2 promoter, luciferase activity is constitutive; and when fused to the promoter of the white-phase-specific gene WH11 or the opaque-phase-specific gene OP4, luciferase activity is phase specific. The Renilla luciferase system can, therefore, be used as a bioluminescent reporter to analyze the strength and developmental regulation of C. albicans promoters.

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Year:  1996        PMID: 8550405      PMCID: PMC177628          DOI: 10.1128/jb.178.1.121-129.1996

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  36 in total

1.  Switching at the cellular level in the white-opaque transition of Candida albicans.

Authors:  M S Bergen; E Voss; D R Soll
Journal:  J Gen Microbiol       Date:  1990-10

Review 2.  High-frequency switching in Candida albicans.

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

3.  Repeated use of GAL1 for gene disruption in Candida albicans.

Authors:  J A Gorman; W Chan; J W Gorman
Journal:  Genetics       Date:  1991-09       Impact factor: 4.562

4.  Isolation and nucleotide sequence of an autonomously replicating sequence (ARS) element functional in Candida albicans and Saccharomyces cerevisiae.

Authors:  R D Cannon; H F Jenkinson; M G Shepherd
Journal:  Mol Gen Genet       Date:  1990-04

5.  Isolation and expression of a cDNA encoding Renilla reniformis luciferase.

Authors:  W W Lorenz; R O McCann; M Longiaru; M J Cormier
Journal:  Proc Natl Acad Sci U S A       Date:  1991-05-15       Impact factor: 11.205

6.  Molecular cloning and expression in Escherichia coli of a cDNA clone encoding luciferase of a firefly, Luciola lateralis.

Authors:  H Tatsumi; N Kajiyama; E Nakano
Journal:  Biochim Biophys Acta       Date:  1992-06-15

7.  Cloning, sequencing and chromosomal assignment of a gene from Saccharomyces cerevisiae which is negatively regulated by glucose and positively by lipids.

Authors:  R L Stone; V Matarese; B B Magee; P T Magee; D A Bernlohr
Journal:  Gene       Date:  1990-12-15       Impact factor: 3.688

8.  Transcription of the gene for a pepsinogen, PEP1, is regulated by white-opaque switching in Candida albicans.

Authors:  B Morrow; T Srikantha; D R Soll
Journal:  Mol Cell Biol       Date:  1992-07       Impact factor: 4.272

9.  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

10.  PHR1, a pH-regulated gene of Candida albicans, is required for morphogenesis.

Authors:  S M Saporito-Irwin; C E Birse; P S Sypherd; W A Fonzi
Journal:  Mol Cell Biol       Date:  1995-02       Impact factor: 4.272

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  50 in total

1.  Misexpression of the opaque-phase-specific gene PEP1 (SAP1) in the white phase of Candida albicans confers increased virulence in a mouse model of cutaneous infection.

Authors:  C Kvaal; S A Lachke; T Srikantha; K Daniels; J McCoy; D R Soll
Journal:  Infect Immun       Date:  1999-12       Impact factor: 3.441

2.  EFG1 null mutants of Candida albicans switch but cannot express the complete phenotype of white-phase budding cells.

Authors:  T Srikantha; L K Tsai; K Daniels; D R Soll
Journal:  J Bacteriol       Date:  2000-03       Impact factor: 3.490

3.  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

Review 4.  Molecular genetic and genomic approaches to the study of medically important fungi.

Authors:  P T Magee; Cheryl Gale; Judith Berman; Dana Davis
Journal:  Infect Immun       Date:  2003-05       Impact factor: 3.441

Review 5.  Strategies for the identification of virulence determinants in human pathogenic fungi.

Authors:  R Alonso-Monge; F Navarro-García; E Román; B Eisman; C Nombela; J Pla
Journal:  Curr Genet       Date:  2003-02-08       Impact factor: 3.886

Review 6.  Milestones in Candida albicans gene manipulation.

Authors:  Dhanushki P Samaranayake; Steven D Hanes
Journal:  Fungal Genet Biol       Date:  2011-04-14       Impact factor: 3.495

7.  Hemoglobin regulates expression of an activator of mating-type locus alpha genes in Candida albicans.

Authors:  Michael L Pendrak; S Steve Yan; David D Roberts
Journal:  Eukaryot Cell       Date:  2004-06

8.  The UPC2 promoter in Candida albicans contains two cis-acting elements that bind directly to Upc2p, resulting in transcriptional autoregulation.

Authors:  Samantha J Hoot; Ryan P Brown; Brian G Oliver; Theodore C White
Journal:  Eukaryot Cell       Date:  2010-07-23

9.  Dual luciferase assay system for rapid assessment of gene expression in Saccharomyces cerevisiae.

Authors:  David S McNabb; Robin Reed; Robert A Marciniak
Journal:  Eukaryot Cell       Date:  2005-09

10.  Green fluorescent protein is a quantitative reporter of gene expression in individual eukaryotic cells.

Authors:  Mark R Soboleski; Jason Oaks; William P Halford
Journal:  FASEB J       Date:  2005-01-07       Impact factor: 5.191

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