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TFCONES: A database of vertebrate transcription factor-encoding genes and their associated conserved noncoding elements
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...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2148067/ https://www.ncbi.nlm.nih.gov/pubmed/18045502 http://dx.doi.org/10.1186/1471-2164-8-441 |
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author | Lee, Alison P Yang, Yuchen Brenner, Sydney Venkatesh, Byrappa |
author_facet | Lee, Alison P Yang, Yuchen Brenner, Sydney Venkatesh, Byrappa |
author_sort | Lee, Alison P |
collection | PubMed |
description | 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) () 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. |
format | Text |
id | pubmed-2148067 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-21480672007-12-20 TFCONES: A database of vertebrate transcription factor-encoding genes and their associated conserved noncoding elements Lee, Alison P Yang, Yuchen Brenner, Sydney Venkatesh, Byrappa BMC Genomics Database 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) () 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. BioMed Central 2007-11-29 /pmc/articles/PMC2148067/ /pubmed/18045502 http://dx.doi.org/10.1186/1471-2164-8-441 Text en Copyright © 2007 Lee et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Database Lee, Alison P Yang, Yuchen Brenner, Sydney Venkatesh, Byrappa TFCONES: A database of vertebrate transcription factor-encoding genes and their associated conserved noncoding elements |
title | TFCONES: A database of vertebrate transcription factor-encoding genes and their associated conserved noncoding elements |
title_full | TFCONES: A database of vertebrate transcription factor-encoding genes and their associated conserved noncoding elements |
title_fullStr | TFCONES: A database of vertebrate transcription factor-encoding genes and their associated conserved noncoding elements |
title_full_unstemmed | TFCONES: A database of vertebrate transcription factor-encoding genes and their associated conserved noncoding elements |
title_short | TFCONES: A database of vertebrate transcription factor-encoding genes and their associated conserved noncoding elements |
title_sort | tfcones: a database of vertebrate transcription factor-encoding genes and their associated conserved noncoding elements |
topic | Database |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2148067/ https://www.ncbi.nlm.nih.gov/pubmed/18045502 http://dx.doi.org/10.1186/1471-2164-8-441 |
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