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Anatomy of Escherichia coli σ(70) promoters
Information theory was used to build a promoter model that accounts for the −10, the −35 and the uncertainty of the gap between them on a common scale. Helical face assignment indicated that base −7, rather than −11, of the −10 may be flipping to initiate transcription. We found that the sequence co...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1807945/ https://www.ncbi.nlm.nih.gov/pubmed/17189297 http://dx.doi.org/10.1093/nar/gkl956 |
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author | Shultzaberger, Ryan K. Chen, Zehua Lewis, Karen A. Schneider, Thomas D. |
author_facet | Shultzaberger, Ryan K. Chen, Zehua Lewis, Karen A. Schneider, Thomas D. |
author_sort | Shultzaberger, Ryan K. |
collection | PubMed |
description | Information theory was used to build a promoter model that accounts for the −10, the −35 and the uncertainty of the gap between them on a common scale. Helical face assignment indicated that base −7, rather than −11, of the −10 may be flipping to initiate transcription. We found that the sequence conservation of σ(70) binding sites is 6.5 ± 0.1 bits. Some promoters lack a −35 region, but have a 6.7 ± 0.2 bit extended −10, almost the same information as the bipartite promoter. These results and similarities between the contacts in the extended −10 binding and the −35 suggest that the flexible bipartite σ factor evolved from a simpler polymerase. Binding predicted by the bipartite model is enriched around 35 bases upstream of the translational start. This distance is the smallest 5′ mRNA leader necessary for ribosome binding, suggesting that selective pressure minimizes transcript length. The promoter model was combined with models of the transcription factors Fur and Lrp to locate new promoters, to quantify promoter strengths, and to predict activation and repression. Finally, the DNA-bending proteins Fis, H-NS and IHF frequently have sites within one DNA persistence length from the −35, so bending allows distal activators to reach the polymerase. |
format | Text |
id | pubmed-1807945 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-18079452007-03-02 Anatomy of Escherichia coli σ(70) promoters Shultzaberger, Ryan K. Chen, Zehua Lewis, Karen A. Schneider, Thomas D. Nucleic Acids Res Computational Biology Information theory was used to build a promoter model that accounts for the −10, the −35 and the uncertainty of the gap between them on a common scale. Helical face assignment indicated that base −7, rather than −11, of the −10 may be flipping to initiate transcription. We found that the sequence conservation of σ(70) binding sites is 6.5 ± 0.1 bits. Some promoters lack a −35 region, but have a 6.7 ± 0.2 bit extended −10, almost the same information as the bipartite promoter. These results and similarities between the contacts in the extended −10 binding and the −35 suggest that the flexible bipartite σ factor evolved from a simpler polymerase. Binding predicted by the bipartite model is enriched around 35 bases upstream of the translational start. This distance is the smallest 5′ mRNA leader necessary for ribosome binding, suggesting that selective pressure minimizes transcript length. The promoter model was combined with models of the transcription factors Fur and Lrp to locate new promoters, to quantify promoter strengths, and to predict activation and repression. Finally, the DNA-bending proteins Fis, H-NS and IHF frequently have sites within one DNA persistence length from the −35, so bending allows distal activators to reach the polymerase. Oxford University Press 2007-02 2006-12-22 /pmc/articles/PMC1807945/ /pubmed/17189297 http://dx.doi.org/10.1093/nar/gkl956 Text en Published by Oxford University Press 2006 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Computational Biology Shultzaberger, Ryan K. Chen, Zehua Lewis, Karen A. Schneider, Thomas D. Anatomy of Escherichia coli σ(70) promoters |
title | Anatomy of Escherichia coli σ(70) promoters |
title_full | Anatomy of Escherichia coli σ(70) promoters |
title_fullStr | Anatomy of Escherichia coli σ(70) promoters |
title_full_unstemmed | Anatomy of Escherichia coli σ(70) promoters |
title_short | Anatomy of Escherichia coli σ(70) promoters |
title_sort | anatomy of escherichia coli σ(70) promoters |
topic | Computational Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1807945/ https://www.ncbi.nlm.nih.gov/pubmed/17189297 http://dx.doi.org/10.1093/nar/gkl956 |
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