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The features of Drosophila core promoters revealed by statistical analysis

BACKGROUND: Experimental investigation of transcription is still a very labor- and time-consuming process. Only a few transcription initiation scenarios have been studied in detail. The mechanism of interaction between basal machinery and promoter, in particular core promoter elements, is not known...

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Autores principales: Gershenzon, Naum I, Trifonov, Edward N, Ioshikhes, Ilya P
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1538597/
https://www.ncbi.nlm.nih.gov/pubmed/16790048
http://dx.doi.org/10.1186/1471-2164-7-161
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author Gershenzon, Naum I
Trifonov, Edward N
Ioshikhes, Ilya P
author_facet Gershenzon, Naum I
Trifonov, Edward N
Ioshikhes, Ilya P
author_sort Gershenzon, Naum I
collection PubMed
description BACKGROUND: Experimental investigation of transcription is still a very labor- and time-consuming process. Only a few transcription initiation scenarios have been studied in detail. The mechanism of interaction between basal machinery and promoter, in particular core promoter elements, is not known for the majority of identified promoters. In this study, we reveal various transcription initiation mechanisms by statistical analysis of 3393 nonredundant Drosophila promoters. RESULTS: Using Drosophila-specific position-weight matrices, we identified promoters containing TATA box, Initiator, Downstream Promoter Element (DPE), and Motif Ten Element (MTE), as well as core elements discovered in Human (TFIIB Recognition Element (BRE) and Downstream Core Element (DCE)). Promoters utilizing known synergetic combinations of two core elements (TATA_Inr, Inr_MTE, Inr_DPE, and DPE_MTE) were identified. We also establish the existence of promoters with potentially novel synergetic combinations: TATA_DPE and TATA_MTE. Our analysis revealed several motifs with the features of promoter elements, including possible novel core promoter element(s). Comparison of Human and Drosophila showed consistent percentages of promoters with TATA, Inr, DPE, and synergetic combinations thereof, as well as most of the same functional and mutual positions of the core elements. No statistical evidence of MTE utilization in Human was found. Distinct nucleosome positioning in particular promoter classes was revealed. CONCLUSION: We present lists of promoters that potentially utilize the aforementioned elements/combinations. The number of these promoters is two orders of magnitude larger than the number of promoters in which transcription initiation was experimentally studied. The sequences are ready to be experimentally tested or used for further statistical analysis. The developed approach may be utilized for other species.
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spelling pubmed-15385972006-08-10 The features of Drosophila core promoters revealed by statistical analysis Gershenzon, Naum I Trifonov, Edward N Ioshikhes, Ilya P BMC Genomics Research Article BACKGROUND: Experimental investigation of transcription is still a very labor- and time-consuming process. Only a few transcription initiation scenarios have been studied in detail. The mechanism of interaction between basal machinery and promoter, in particular core promoter elements, is not known for the majority of identified promoters. In this study, we reveal various transcription initiation mechanisms by statistical analysis of 3393 nonredundant Drosophila promoters. RESULTS: Using Drosophila-specific position-weight matrices, we identified promoters containing TATA box, Initiator, Downstream Promoter Element (DPE), and Motif Ten Element (MTE), as well as core elements discovered in Human (TFIIB Recognition Element (BRE) and Downstream Core Element (DCE)). Promoters utilizing known synergetic combinations of two core elements (TATA_Inr, Inr_MTE, Inr_DPE, and DPE_MTE) were identified. We also establish the existence of promoters with potentially novel synergetic combinations: TATA_DPE and TATA_MTE. Our analysis revealed several motifs with the features of promoter elements, including possible novel core promoter element(s). Comparison of Human and Drosophila showed consistent percentages of promoters with TATA, Inr, DPE, and synergetic combinations thereof, as well as most of the same functional and mutual positions of the core elements. No statistical evidence of MTE utilization in Human was found. Distinct nucleosome positioning in particular promoter classes was revealed. CONCLUSION: We present lists of promoters that potentially utilize the aforementioned elements/combinations. The number of these promoters is two orders of magnitude larger than the number of promoters in which transcription initiation was experimentally studied. The sequences are ready to be experimentally tested or used for further statistical analysis. The developed approach may be utilized for other species. BioMed Central 2006-06-21 /pmc/articles/PMC1538597/ /pubmed/16790048 http://dx.doi.org/10.1186/1471-2164-7-161 Text en Copyright © 2006 Gershenzon 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 Research Article
Gershenzon, Naum I
Trifonov, Edward N
Ioshikhes, Ilya P
The features of Drosophila core promoters revealed by statistical analysis
title The features of Drosophila core promoters revealed by statistical analysis
title_full The features of Drosophila core promoters revealed by statistical analysis
title_fullStr The features of Drosophila core promoters revealed by statistical analysis
title_full_unstemmed The features of Drosophila core promoters revealed by statistical analysis
title_short The features of Drosophila core promoters revealed by statistical analysis
title_sort features of drosophila core promoters revealed by statistical analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1538597/
https://www.ncbi.nlm.nih.gov/pubmed/16790048
http://dx.doi.org/10.1186/1471-2164-7-161
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