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PMID: 12832287 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Computer modeling of promoter organization as a tool to study transcriptional coregulation.

Werner T, Fessele S, Maier H, Nelson PJ

Abstract

Understanding how the regulation of gene networks is orchestrated is an important challenge for characterizing complex biological processes. Gene transcription is regulated in part by nuclear factors that recognize short DNA sequence motifs, called transcription factor binding sites, in most cases located upstream of the gene coding sequence in promoter and enhancer regions. Genes expressed in the same tissue under similar conditions often share a common organization of at least some of these regulatory binding elements. In this way the organization of promoter motifs represents a "footprint" of the transcriptional regulatory mechanisms at work in a specific biologic context and thus provides information about signal and tissue specific control of expression. Analysis of promoters for organizational features as demonstrated here provides a crucial link between the static nucleotide sequence of the genome and the dynamic aspects of gene regulation and expression.

MeSH Terms
Animals Astrocytes/metabolism Chemokine CCL5/biosynthesis,genetics Computer Simulation Gene Expression Regulation Glomerular Mesangium/cytology,metabolism Humans Models, Genetic Monocytes/immunology Organ Specificity Promoter Regions, Genetic Signal Transduction T-Lymphocytes/immunology Transcription, Genetic
Chemicals
Chemokine CCL5
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Werner Thomas
GSF-National Research Center for Environment and Health, Institute of Experimental Genetics, Neuherberg, Germany.
Fessele Sabine
Maier Holge
Nelson Peter J
Article Info
Journal
FASEB journal : official publication of the Federation of American Societies for Experimental Biology
Abbr.
FASEB J
ISSN
1530-6860
Published
2003-07-00
Pages
1228-37
Language
English
Region
United States
NLM ID
8804484
Subset
IM
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