Evidence map›Paper›PMID 7874734›Full record

ArticleCurrent genetics

MluI site-dependent transcriptional regulation of the Candida albicans dUTPase gene.

E M McIntosh, J Looser, R H Haynes, R E Pearlman

Erratum issuedOpen access · bronzeAbstract readComparative Study
PubMed Publisher
In one paragraph

Article in Current genetics. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.4field-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

3 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Kinetic properties and inhibition of the dimeric dUTPase-dUDPase from Leishmania major.Protein science : a publication of the Protein Society · 2001
    Article
  3. Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

E M McIntoshDepartment of Biology, University of York, Toronto, Ontario, Canada.
J Looser
R H Haynes
R E Pearlman
York University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Candida albicans dUTP pyrophosphatase (dUTPase) gene DUT1 has been isolated by genetic complementation in S. cerevisiae. It was found to encode a 17-kDa protein similar in amino-acid sequence to dUTPases isolated from other systems. The gene was adapted for expression in E. coli and yielded a soluble and highly-active enzyme which is easily purified. The 5' flanking sequence of DUT1 contains an MluI site typical of MCB cell-cycle-dependent UAS elements of budding and fission yeast. We found the gene to be cell-cycle-regulated when expressed in S. cerevisiae, and deletion of the MluI site resulted in a large reduction of DUT1 transcription in C. albicans. These results suggest that MCB elements are functionally conserved in this pathogenic fungus. Based on the vital role that dUTPase plays in DNA replication, the C. albicans enzyme may be a potentially useful target for the development of novel anti-fungal compounds.

Indexed as

Bacterial ProteinsGene Expression Regulation, EnzymologicGene Expression Regulation, FungalGenes, FungalAmino Acid SequenceBase SequenceBlotting, NorthernCandida albicansCloning, MolecularDeoxyribonucleases, Type II Site-SpecificDNA PrimersDNA ReplicationEscherichia coliHumansImmunodeficiency Virus, FelineMolecular Sequence DataBacterial ProteinsDeoxyribonucleases, Type II Site-SpecificDNA PrimersdUTP pyrophosphataseendodeoxyribonuclease MluIPyrophosphatasesRecombinant ProteinsRNA, Fungal

Identifiers

PMID7874734
OpenAlexW1969889323

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.