Evidence map›Paper›PMID 11741841›Full record

ArticleJournal of bacteriology2002

Molecular and phenotypic analysis of CaVRG4, encoding an essential Golgi apparatus GDP-mannose transporter.

Akiko Nishikawa, Jay B Poster, Yoshifumi Jigami, Neta Dean

Open access · greenAbstract read
In one paragraph

Article in Journal of bacteriology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

35 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Journal of fungi (Basel, Switzerland) · 2024
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Galactomannan Produced byJournal of fungi (Basel, Switzerland) · 2020
    Review
  8. Article
  9. The Role of Secretory Pathways inJournal of fungi (Basel, Switzerland) · 2020
    Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Virulence Factors as Targets for Anticryptococcal Therapy.Journal of fungi (Basel, Switzerland) · 2016
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Reporters for the analysis of N-glycosylation in Candida albicans.Fungal genetics and biology : FG & B · 2013
    Article
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

4 authors at 3 institutions in 2 countries.

Akiko NishikawaDepartment of Biochemistry and Cell Biology, Institute for Cell and Developmental Biology, State University of New York, Stony Brook, New York 11794-5215, USA.
Jay B Poster
Yoshifumi Jigami
Neta Dean
State University of New York · USNational Institute of Advanced Industrial Science and Technology · JPStony Brook University · US

Funding

PROTEIN TARGETING TO THE YEAST GOLGIR01GM048467 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI DEAN, NETA · 1995 to 2006
$2.3M
NIGMS NIH HHS GM48467NIGMS NIH HHS R01 GM048467
6 · The paper itself

Abstract

Cell surface mannan is implicated in almost every aspect of pathogenicity of Candida albicans. In Saccharomyces cerevisiae, the Vrg4 protein acts as a master regulator of mannan synthesis through its role in substrate provision. The substrate for mannosylation of proteins and lipids in the Golgi apparatus is GDP-mannose, whose lumenal transport is catalyzed by Vrg4p. This nucleotide sugar is synthesized in the cytoplasm by pathways that are highly conserved in all eukaryotes, but its lumenal transport (and hence Golgi apparatus-specific mannosylation) is a fungus-specific process. To begin to study the role of Golgi mannosylation in C. albicans, we isolated the CaVRG4 gene and analyzed the effects of loss of its function. CaVRG4 encodes a functional homologue of the S. cerevisiae GDP-mannose transporter. CaVrg4p localized to punctate spots within the cytoplasm of C. albicans in a pattern reminiscent of localization of Vrg4p in the Golgi apparatus in S. cerevisiae. Like partial loss of ScVRG4 function, partial loss of CaVRG4 function resulted in mannosylation defects, which in turn led to a number of cell wall-associated phenotypes. While heterozygotes displayed no growth phenotypes, a hemizygous strain, containing a single copy of CaVRG4 under control of the methionine-repressible MET3 promoter, did not grow in the presence of methionine and cysteine, demonstrating that CaVRG4 is essential for viability. Mutant Candida vrg4 strains were defective in hyphal formation but exhibited a constitutive polarized mode of pseudohyphal growth. Because the VRG4 gene is essential for yeast viability but does not have a mammalian homologue, it is a particularly attractive target for development of antifungal therapies.

Indexed as

Amino Acid SequenceCandida albicansFungal ProteinsGenes, EssentialGenes, FungalGlycosylationGolgi ApparatusMannansMembrane Transport ProteinsMolecular Sequence DataMorphogenesisMutationSaccharomyces cerevisiae ProteinsSequence Homology, Amino AcidFungal ProteinsMannansMembrane Transport ProteinsSaccharomyces cerevisiae ProteinsVRG4 protein, Candida albicansVRG4 protein, S cerevisiae

Identifiers

PMID11741841
PMCPMC134776
OpenAlexW2126826742

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.