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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...

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Autores principales: Jin, Victor X, Singer, Gregory AC, Agosto-Pérez, Francisco J, Liyanarachchi, Sandya, Davuluri, Ramana V
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
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.
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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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