Evidence map›Paper›PMID 27294345›Full record

ArticleBMC bioinformatics2016

Analysis tools for the interplay between genome layout and regulation.

Costas Bouyioukos, Mohamed Elati, François Képès

Abstract read
In one paragraph

Article in BMC bioinformatics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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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

2 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.

Costas Bouyioukosinstitute of Systems and Synthetic Biology (iSSB), Genopole, CNRS, Université d'Évry Val d'Essonne, Évry, France.
Mohamed Elatiinstitute of Systems and Synthetic Biology (iSSB), Genopole, CNRS, Université d'Évry Val d'Essonne, Évry, France.
François Képèsinstitute of Systems and Synthetic Biology (iSSB), Genopole, CNRS, Université d'Évry Val d'Essonne, Évry, France. francois.kepes@issb.genopole.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGenome layout and gene regulation appear to be interdependent. Understanding this interdependence is key to exploring the dynamic nature of chromosome conformation and to engineering functional genomes. Evidence for non-random genome layout, defined as the relative positioning of either co-functional or co-regulated genes, stems from two main approaches. Firstly, the analysis of contiguous genome segments across species, has highlighted the conservation of gene arrangement (synteny) along chromosomal regions. Secondly, the study of long-range interactions along a chromosome has emphasised regularities in the positioning of microbial genes that are co-regulated, co-expressed or evolutionarily correlated. While one-dimensional pattern analysis is a mature field, it is often powerless on biological datasets which tend to be incomplete, and partly incorrect. Moreover, there is a lack of comprehensive, user-friendly tools to systematically analyse, visualise, integrate and exploit regularities along genomes.

resultsHere we present the Genome REgulatory and Architecture Tools SCAN (GREAT:SCAN) software for the systematic study of the interplay between genome layout and gene expression regulation. GREAT: SCAN is a collection of related and interconnected applications currently able to perform systematic analyses of genome regularities as well as to improve transcription factor binding sites (TFBS) and gene regulatory network predictions based on gene positional information.

conclusionsWe demonstrate the capabilities of these tools by studying on one hand the regular patterns of genome layout in the major regulons of the bacterium Escherichia coli. On the other hand, we demonstrate the capabilities to improve TFBS prediction in microbes. Finally, we highlight, by visualisation of multivariate techniques, the interplay between position and sequence information for effective transcription regulation.

Indexed as

GenomeSoftwareBinding SitesEscherichia coliEscherichia coli ProteinsGene Regulatory NetworksTranscription FactorsEscherichia coli ProteinsTranscription FactorsChromosome conformationGenome expression regulationGenome organisationGenome patterns

Identifiers

PMID27294345
PMCPMC4905612

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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.