Evidence map›Paper›PMID 15115798›Full record

ArticleNucleic acids research2004

Transcription factor binding element detection using functional clustering of mutant expression data.

Gengxin Chen, Naoya Hata, Michael Q Zhang

Abstract read
In one paragraph

Article in Nucleic acids research, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

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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.

Gengxin ChenCold Spring Harbor Laboratory, 1 Bungtown Road, Cold Spring Harbor, NY 11724, USA.
Naoya Hata
Michael Q Zhang

Funding

COMPUTATIONAL ANALYSIS OF GENOME EXPRESSION DATAR01GM060513 · NIGMS · COLD SPRING HARBOR LABORATORY · PI ZHANG, MICHAEL Q · 2000 to 2002
$898k
NIGMS NIH HHS GM60513NIGMS NIH HHS R01 GM060513
6 · The paper itself

Abstract

As a powerful tool to reveal gene functions, gene mutation has been used extensively in molecular biology studies. With high throughput technologies, such as DNA microarray, genome-wide gene expression changes can be monitored in mutants. Here we present a simple approach to detect the transcription-factor-binding motif using microarray expression data from a mutant in which the relevant transcription factor is deleted. A core part of our approach is clustering of differentially expressed genes based on functional annotations, such as Gene Ontology (GO). We tested our method with eight microarray data sets from the Rosetta Compendium and were able to detect canonical binding motifs for at least four transcription factors. With the support of chromatin IP chip data, we also predict a possible variant of the Swi4 binding motif and recover a core motif for Arg80. Our approach should be readily applicable to microarray experiments using other types of molecular biology techniques, such as conditional knockout/overexpression or RNAi-mediated 'knockdown', to perturb the expression of a transcription factor. Functional clustering included in our approach may also provide new insights into the function of the relevant transcription factor.

Indexed as

Gene DeletionBase SequenceCluster AnalysisComputational BiologyConsensus SequenceGene Expression ProfilingGenes, FungalGenomicsOligonucleotide Array Sequence AnalysisReproducibility of ResultsResponse ElementsSaccharomyces cerevisiae ProteinsSoftwareTranscription FactorsSaccharomyces cerevisiae ProteinsTranscription Factors

Identifiers

PMID15115798
PMCPMC419446

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.