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Genome-wide analysis of core promoter elements from conserved human and mouse orthologous pairs
BACKGROUND: The canonical core promoter elements consist of the TATA box, initiator (Inr), downstream core promoter element (DPE), TFIIB recognition element (BRE) and the newly-discovered motif 10 element (MTE). The motifs for these core promoter elements are highly degenerate, which tends to lead t...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1475891/ https://www.ncbi.nlm.nih.gov/pubmed/16522199 http://dx.doi.org/10.1186/1471-2105-7-114 |
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author | Jin, Victor X Singer, Gregory AC Agosto-Pérez, Francisco J Liyanarachchi, Sandya Davuluri, Ramana V |
author_facet | Jin, Victor X Singer, Gregory AC Agosto-Pérez, Francisco J Liyanarachchi, Sandya Davuluri, Ramana V |
author_sort | Jin, Victor X |
collection | PubMed |
description | BACKGROUND: The canonical core promoter elements consist of the TATA box, initiator (Inr), downstream core promoter element (DPE), TFIIB recognition element (BRE) and the newly-discovered motif 10 element (MTE). The motifs for these core promoter elements are highly degenerate, which tends to lead to a high false discovery rate when attempting to detect them in promoter sequences. RESULTS: In this study, we have performed the first analysis of these core promoter elements in orthologous mouse and human promoters with experimentally-supported transcription start sites. We have identified these various elements using a combination of positional weight matrices (PWMs) and the degree of conservation of orthologous mouse and human sequences – a procedure that significantly reduces the false positive rate of motif discovery. Our analysis of 9,010 orthologous mouse-human promoter pairs revealed two combinations of three-way synergistic effects, TATA-Inr-MTE and BRE-Inr-MTE. The former has previously been putatively identified in human, but the latter represents a novel synergistic relationship. CONCLUSION: Our results demonstrate that DNA sequence conservation can greatly improve the identification of functional core promoter elements in the human genome. The data also underscores the importance of synergistic occurrence of two or more core promoter elements. Furthermore, the sequence data and results presented here can help build better computational models for predicting the transcription start sites in the promoter regions, which remains one of the most challenging problems. |
format | Text |
id | pubmed-1475891 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-14758912006-06-10 Genome-wide analysis of core promoter elements from conserved human and mouse orthologous pairs Jin, Victor X Singer, Gregory AC Agosto-Pérez, Francisco J Liyanarachchi, Sandya Davuluri, Ramana V BMC Bioinformatics Research Article BACKGROUND: The canonical core promoter elements consist of the TATA box, initiator (Inr), downstream core promoter element (DPE), TFIIB recognition element (BRE) and the newly-discovered motif 10 element (MTE). The motifs for these core promoter elements are highly degenerate, which tends to lead to a high false discovery rate when attempting to detect them in promoter sequences. RESULTS: In this study, we have performed the first analysis of these core promoter elements in orthologous mouse and human promoters with experimentally-supported transcription start sites. We have identified these various elements using a combination of positional weight matrices (PWMs) and the degree of conservation of orthologous mouse and human sequences – a procedure that significantly reduces the false positive rate of motif discovery. Our analysis of 9,010 orthologous mouse-human promoter pairs revealed two combinations of three-way synergistic effects, TATA-Inr-MTE and BRE-Inr-MTE. The former has previously been putatively identified in human, but the latter represents a novel synergistic relationship. CONCLUSION: Our results demonstrate that DNA sequence conservation can greatly improve the identification of functional core promoter elements in the human genome. The data also underscores the importance of synergistic occurrence of two or more core promoter elements. Furthermore, the sequence data and results presented here can help build better computational models for predicting the transcription start sites in the promoter regions, which remains one of the most challenging problems. BioMed Central 2006-03-07 /pmc/articles/PMC1475891/ /pubmed/16522199 http://dx.doi.org/10.1186/1471-2105-7-114 Text en Copyright © 2006 Jin et al; licensee BioMed Central Ltd. |
spellingShingle | Research Article Jin, Victor X Singer, Gregory AC Agosto-Pérez, Francisco J Liyanarachchi, Sandya Davuluri, Ramana V Genome-wide analysis of core promoter elements from conserved human and mouse orthologous pairs |
title | Genome-wide analysis of core promoter elements from conserved human and mouse orthologous pairs |
title_full | Genome-wide analysis of core promoter elements from conserved human and mouse orthologous pairs |
title_fullStr | Genome-wide analysis of core promoter elements from conserved human and mouse orthologous pairs |
title_full_unstemmed | Genome-wide analysis of core promoter elements from conserved human and mouse orthologous pairs |
title_short | Genome-wide analysis of core promoter elements from conserved human and mouse orthologous pairs |
title_sort | genome-wide analysis of core promoter elements from conserved human and mouse orthologous pairs |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1475891/ https://www.ncbi.nlm.nih.gov/pubmed/16522199 http://dx.doi.org/10.1186/1471-2105-7-114 |
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