Evidence map›Paper›PMID 8082184›Full record

ArticleCurrent genetics1994

Approaching the function of new genes by detection of their potential upstream activation sequences in Saccharomyces cerevisiae: application to chromosome III.

C Fondrat, A Kalogeropoulos

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Article in Current genetics, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Quantitative discrimination of MEF2 sites.Molecular and cellular biology · 1996
    Article
  6. 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

2 authors.

C FondratInstitut de Génétique et Microbiologie, Centre Universitaire d'Orsay, France.
A Kalogeropoulos

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The systematic sequencing of the yeast genome reveals the presence of many potential genes of unknown function. One way to approach their function is to define which regulatory system controls their transcription. This can also be accomplished by the detection of an upstream activation sequence (UAS). Such a detection can be done by computer, provided that the definition of a UAS includes sufficient and precise rules. We have established such rules for the UASs of the GAL4, RAP1 (RPG box), GCN4, and the HAP2/HAP3/HAP4 regulatory proteins, as well as for a motif (PAC) frequently found upstream of the genes of the RNA polymerase A and C subunits. These rules were applied to the chromosome III DNA sequence, and gave precise predictions.

Indexed as

CCAAT-Binding FactorChromosomes, FungalDNA-Binding ProteinsGenes, FungalSaccharomyces cerevisiae ProteinsBase SequenceConsensus SequenceDNA, FungalFungal ProteinsGene Expression Regulation, FungalMolecular Sequence DataOpen Reading FramesProtein KinasesRibosomal ProteinsSaccharomyces cerevisiaeTranscription FactorsCCAAT-Binding FactorDNA-Binding ProteinsDNA, FungalFungal ProteinsGAL4 protein, S cerevisiaeHAP4 protein, S cerevisiaeProtein KinasesRibosomal ProteinsSaccharomyces cerevisiae ProteinsTranscription Factors

Identifiers

PMID8082184

What OpenQuestion holds

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Registered trials

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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.