Please use this identifier to cite or link to this item: https://doi.org/10.1186/1471-2164-8-441
Title: TFCONES: A database of vertebrate transcription factor-encoding genes and their associated conserved noncoding elements
Authors: Lee, A.P
Yang, Y
Brenner, S 
Venkatesh, B 
Keywords: DNA binding protein
Myc protein
octamer transcription factor 4
transcription factor
transcription factor Sox2
transcription factor
article
binding site
cancer inhibition
cell cycle progression
cell differentiation
cell maturation
comparative genomic hybridization
data base
DNA binding
DNA flanking region
gene cluster
gene identification
gene locus
gene mapping
genetic code
genetic database
human
nonhuman
protein protein interaction
regulatory sequence
Transcription Factor Genes and Associated COnserved Noncoding ElementS database
transcription regulation
animal
genetics
Internet
vertebrate
Takifugu
Vertebrata
Animals
Databases, Genetic
Humans
Internet
Transcription Factors
Vertebrates
Issue Date: 2007
Citation: Lee, A.P, Yang, Y, Brenner, S, Venkatesh, B (2007). TFCONES: A database of vertebrate transcription factor-encoding genes and their associated conserved noncoding elements. BMC Genomics 8 : 441. ScholarBank@NUS Repository. https://doi.org/10.1186/1471-2164-8-441
Rights: Attribution 4.0 International
Abstract: Background: Transcription factors (TFs) regulate gene transcription and play pivotal roles in various biological processes such as development, cell cycle progression, cell differentiation and tumor suppression. Identifying cis-regulatory elements associated with TF-encoding genes is a crucial step in understanding gene regulatory networks. To this end, we have used a comparative genomics approach to identify putative cis-regulatory elements associated with TF-encoding genes in vertebrates. Description: We have created a database named TFCONES (Transcription Factor Genes & Associated COnserved Noncoding ElementS) (http://tfcones.fugu-sg.org) which contains all human, mouse and fugu TF-encoding genes and conserved noncoding elements (CNEs) associated with them. The CNEs were identified by gene-by-gene alignments of orthologous TF-encoding gene loci using MLAGAN. We also predicted putative transcription factor binding sites within the CNEs. A significant proportion of human-fugu CNEs contain experimentally defined binding sites for transcriptional activators and repressors, indicating that a majority of the CNEs may function as transcriptional regulatory elements. The TF-encoding genes that are involved in nervous system development are generally enriched for human-fugu CNEs. Users can retrieve TF-encoding genes and their associated CNEs by conducting a keyword search or by selecting a family of DNA-binding proteins. Conclusion: The conserved noncoding elements identified in TFCONES represent a catalog of highly prioritized putative cis-regulatory elements of TF-encoding genes and are candidates for functional assay. © 2007 Lee et al; licensee BioMed Central Ltd.
Source Title: BMC Genomics
URI: https://scholarbank.nus.edu.sg/handle/10635/177985
ISSN: 14712164
DOI: 10.1186/1471-2164-8-441
Rights: Attribution 4.0 International
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