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Unravelling the hidden DNA structural/physical code provides novel insights on promoter location
Although protein recognition of DNA motifs in promoter regions has been traditionally considered as a critical regulatory element in transcription, the location of promoters, and in particular transcription start sites (TSSs), still remains a challenge. Here we perform a comprehensive analysis of pu...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3753636/ https://www.ncbi.nlm.nih.gov/pubmed/23761436 http://dx.doi.org/10.1093/nar/gkt511 |
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author | Durán, Elisa Djebali, Sarah González, Santi Flores, Oscar Mercader, Josep Maria Guigó, Roderic Torrents, David Soler-López, Montserrat Orozco, Modesto |
author_facet | Durán, Elisa Djebali, Sarah González, Santi Flores, Oscar Mercader, Josep Maria Guigó, Roderic Torrents, David Soler-López, Montserrat Orozco, Modesto |
author_sort | Durán, Elisa |
collection | PubMed |
description | Although protein recognition of DNA motifs in promoter regions has been traditionally considered as a critical regulatory element in transcription, the location of promoters, and in particular transcription start sites (TSSs), still remains a challenge. Here we perform a comprehensive analysis of putative core promoter sequences relative to non-annotated predicted TSSs along the human genome, which were defined by distinct DNA physical properties implemented in our ProStar computational algorithm. A representative sampling of predicted regions was subjected to extensive experimental validation and analyses. Interestingly, the vast majority proved to be transcriptionally active despite the lack of specific sequence motifs, indicating that physical signaling is indeed able to detect promoter activity beyond conventional TSS prediction methods. Furthermore, highly active regions displayed typical chromatin features associated to promoters of housekeeping genes. Our results enable to redefine the promoter signatures and analyze the diversity, evolutionary conservation and dynamic regulation of human core promoters at large-scale. Moreover, the present study strongly supports the hypothesis of an ancient regulatory mechanism encoded by the intrinsic physical properties of the DNA that may contribute to the complexity of transcription regulation in the human genome. |
format | Online Article Text |
id | pubmed-3753636 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-37536362013-08-27 Unravelling the hidden DNA structural/physical code provides novel insights on promoter location Durán, Elisa Djebali, Sarah González, Santi Flores, Oscar Mercader, Josep Maria Guigó, Roderic Torrents, David Soler-López, Montserrat Orozco, Modesto Nucleic Acids Res Gene Regulation, Chromatin and Epigenetics Although protein recognition of DNA motifs in promoter regions has been traditionally considered as a critical regulatory element in transcription, the location of promoters, and in particular transcription start sites (TSSs), still remains a challenge. Here we perform a comprehensive analysis of putative core promoter sequences relative to non-annotated predicted TSSs along the human genome, which were defined by distinct DNA physical properties implemented in our ProStar computational algorithm. A representative sampling of predicted regions was subjected to extensive experimental validation and analyses. Interestingly, the vast majority proved to be transcriptionally active despite the lack of specific sequence motifs, indicating that physical signaling is indeed able to detect promoter activity beyond conventional TSS prediction methods. Furthermore, highly active regions displayed typical chromatin features associated to promoters of housekeeping genes. Our results enable to redefine the promoter signatures and analyze the diversity, evolutionary conservation and dynamic regulation of human core promoters at large-scale. Moreover, the present study strongly supports the hypothesis of an ancient regulatory mechanism encoded by the intrinsic physical properties of the DNA that may contribute to the complexity of transcription regulation in the human genome. Oxford University Press 2013-08 2013-06-12 /pmc/articles/PMC3753636/ /pubmed/23761436 http://dx.doi.org/10.1093/nar/gkt511 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Gene Regulation, Chromatin and Epigenetics Durán, Elisa Djebali, Sarah González, Santi Flores, Oscar Mercader, Josep Maria Guigó, Roderic Torrents, David Soler-López, Montserrat Orozco, Modesto Unravelling the hidden DNA structural/physical code provides novel insights on promoter location |
title | Unravelling the hidden DNA structural/physical code provides novel insights on promoter location |
title_full | Unravelling the hidden DNA structural/physical code provides novel insights on promoter location |
title_fullStr | Unravelling the hidden DNA structural/physical code provides novel insights on promoter location |
title_full_unstemmed | Unravelling the hidden DNA structural/physical code provides novel insights on promoter location |
title_short | Unravelling the hidden DNA structural/physical code provides novel insights on promoter location |
title_sort | unravelling the hidden dna structural/physical code provides novel insights on promoter location |
topic | Gene Regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3753636/ https://www.ncbi.nlm.nih.gov/pubmed/23761436 http://dx.doi.org/10.1093/nar/gkt511 |
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