Evidence map›Paper›PMID 15590814›Full record

ArticleEukaryotic cell2004

Role of Candida albicans transcription factor Upc2p in drug resistance and sterol metabolism.

Peter M Silver, Brian G Oliver, Theodore C White

Open access · diamondAbstract read
In one paragraph

Article in Eukaryotic cell, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 137 papers.

0numbers the graph read from it
0cells of the map it votes in
137citing papers in PubMed
2.3field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

137 citing papers in PubMed, 217 citations in OpenAlex.

  1. Review
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  12. Microbiology and molecular biology reviews : MMBR · 2024
    Review
  13. Review
  14. Article
  15. Human Sterols Are Overproduced, Stored and Excreted in Yeasts.International journal of molecular sciences · 2024
    Article
  16. Review
  17. Genome-wide translational response ofMicrobiology spectrum · 2023
    Article
  18. Article
  19. Journal of fungi (Basel, Switzerland) · 2023
    Review
  20. Article

77 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Peter M SilverDepartment of Pathobiology, University of Washington, Seattle, WA, USA.
Brian G Oliver
Theodore C White
Center for Infectious Disease Research · USUniversity of Washington · US

Funding

Diseases of Public Health Importance Training GrantT32AI007509 · NIAID · UNIVERSITY OF WASHINGTON · PI LUND, JENNIFER M · 1997 to 2024
$6.3M
ORAL CANDIDIASIS IN LENTIVIRUS INFECTED MACAQUESR01DE011367 · NIDCR · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI WHITE, THEODORE C. · 1994 to 2007
$2.5M
Azoles and Candida in AIDS - A Whole Cell ResponseR01DE014161 · NIDCR · SEATTLE BIOMEDICAL RESEARCH INSTITUTE · PI WHITE, THEODORE C. · 2001 to 2004
$1.4M
NIAID NIH HHS T32 AI007509NIAID NIH HHS T32 AI07509NIDCR NIH HHS R01 DE011367NIDCR NIH HHS R01 DE014161NIDCR NIH HHS R01 DE11367NIDCR NIH HHS R01 DE14161
6 · The paper itself

Abstract

In Candida albicans, drug resistance to clinically important antifungal drugs may be regulated through the action of transcription factors in a manner that may or may not be similar to regulation in Saccharomyces cerevisiae. A search of the C. albicans genome identified a single homolog of the S. cerevisiae transcription factor genes UPC2 (ScUPC2) and ECM22 (ScECM22) that have been associated with regulation of ergosterol biosynthesis. Sequence analysis of this C. albicans UPC2 (CaUPC2) gene identifies two domains, an anchoring transmembrane domain and a transcription factor region containing multiple nuclear localization signals and a fungal Zn(2)-Cys(6) binuclear cluster domain. Heterozygous deletion, homozygous deletion, and reconstructed strains of CaUPC2 as well as the parental strain were tested against several antifungal drugs, including ergosterol biosynthesis inhibitors. The CaUPC2 homozygous deletion strain showed marked hypersusceptibility to most drugs, compared to the parental and reconstructed strains. The deletion strains accumulate significantly less radiolabeled cholesterol, suggesting reduced ergosterol scavenging in those strains. When grown under azole drug pressure, the parental, heterozygous deletion and reconstructed strains of CaUPC2 upregulate the ERG2 and ERG11 ergosterol biosynthesis genes, while the homozygous deletion strain shows no such upregulation. Consistent with these results, CaUPC2 deletion strains show reduced ergosterol levels, which may explain the increased susceptibilities of the CaUPC2 deletion strains. Thus, it appears that CaUPC2 acts as a transcription factor involved in the regulation of ergosterol biosynthetic genes and as a regulator of sterol uptake across the plasma membrane.

Indexed as

Drug Resistance, FungalBlotting, NorthernBlotting, SouthernCandida albicansCell MembraneCholesterolCulture MediaDNAErgosterolGene DeletionGenotypeHeterozygoteHomozygoteModels, GeneticPlasmidsPolymerase Chain ReactionCholesterolCulture MediaDNAErgosterolSaccharomyces cerevisiae ProteinsSterolsTrans-ActivatorsTranscription FactorsUPC2 protein, S cerevisiae

Identifiers

PMID15590814
PMCPMC539032
OpenAlexW2140936126

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.