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From adjacent activation in Escherichia coli and DNA cyclization to eukaryotic enhancers: the elements of a puzzle

Deoxyribonucleic acid cyclization, Escherichia coli lac repressor binding to two spaced lac operators and repression enhancement can be successfully used for a better understanding of the conditions required for interaction between eukaryotic enhancers and the machinery of transcription initiation....

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Autor principal: Amouyal, Michèle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4217526/
https://www.ncbi.nlm.nih.gov/pubmed/25404937
http://dx.doi.org/10.3389/fgene.2014.00371
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author Amouyal, Michèle
author_facet Amouyal, Michèle
author_sort Amouyal, Michèle
collection PubMed
description Deoxyribonucleic acid cyclization, Escherichia coli lac repressor binding to two spaced lac operators and repression enhancement can be successfully used for a better understanding of the conditions required for interaction between eukaryotic enhancers and the machinery of transcription initiation. Chronologically, the DNA looping model has first accounted for the properties initially defining enhancers, i.e., independence of action with distance or orientation with respect to the start of transcription. It has also predicted enhancer activity or its disruption at short distance (site orientation, alignment between promoter and enhancer sites), with high-order complexes of protein, or with transcription factor concentrations close or different from the wild-type situation. In another step, histones have been introduced into the model to further adapt it to eukaryotes. They in fact favor DNA cyclization in vitro. The resulting DNA compaction might explain the difference counted in base pairs in the distance of action between eukaryotic transcription enhancers and prokaryotic repression enhancers. The lac looping system provides a potential tool for analysis of this discrepancy and of chromatin state directly in situ. Furthermore, as predicted by the model, the contribution of operators O2 and O3 to repression of the lac operon clearly depends on the lac repressor level in the cell and is prevented in strains overproducing lac repressor. By extension, gene regulation especially that linked to cell fate, should also depend on transcription factor levels, providing a potential tool for cellular therapy. In parallel, a new function of the O1–O3 loop completes the picture of lac repression. The O1–O3 loop would at the same time ensure high efficiency of repression, inducibility through the low-affinity sites and limitation of the level of repressor through self-repression of the lac repressor. Last, the DNA looping model can be successfully adapted to the enhancer auxiliary elements known as insulators.
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spelling pubmed-42175262014-11-17 From adjacent activation in Escherichia coli and DNA cyclization to eukaryotic enhancers: the elements of a puzzle Amouyal, Michèle Front Genet Genetics Deoxyribonucleic acid cyclization, Escherichia coli lac repressor binding to two spaced lac operators and repression enhancement can be successfully used for a better understanding of the conditions required for interaction between eukaryotic enhancers and the machinery of transcription initiation. Chronologically, the DNA looping model has first accounted for the properties initially defining enhancers, i.e., independence of action with distance or orientation with respect to the start of transcription. It has also predicted enhancer activity or its disruption at short distance (site orientation, alignment between promoter and enhancer sites), with high-order complexes of protein, or with transcription factor concentrations close or different from the wild-type situation. In another step, histones have been introduced into the model to further adapt it to eukaryotes. They in fact favor DNA cyclization in vitro. The resulting DNA compaction might explain the difference counted in base pairs in the distance of action between eukaryotic transcription enhancers and prokaryotic repression enhancers. The lac looping system provides a potential tool for analysis of this discrepancy and of chromatin state directly in situ. Furthermore, as predicted by the model, the contribution of operators O2 and O3 to repression of the lac operon clearly depends on the lac repressor level in the cell and is prevented in strains overproducing lac repressor. By extension, gene regulation especially that linked to cell fate, should also depend on transcription factor levels, providing a potential tool for cellular therapy. In parallel, a new function of the O1–O3 loop completes the picture of lac repression. The O1–O3 loop would at the same time ensure high efficiency of repression, inducibility through the low-affinity sites and limitation of the level of repressor through self-repression of the lac repressor. Last, the DNA looping model can be successfully adapted to the enhancer auxiliary elements known as insulators. Frontiers Media S.A. 2014-11-03 /pmc/articles/PMC4217526/ /pubmed/25404937 http://dx.doi.org/10.3389/fgene.2014.00371 Text en Copyright © 2014 Amouyal. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Amouyal, Michèle
From adjacent activation in Escherichia coli and DNA cyclization to eukaryotic enhancers: the elements of a puzzle
title From adjacent activation in Escherichia coli and DNA cyclization to eukaryotic enhancers: the elements of a puzzle
title_full From adjacent activation in Escherichia coli and DNA cyclization to eukaryotic enhancers: the elements of a puzzle
title_fullStr From adjacent activation in Escherichia coli and DNA cyclization to eukaryotic enhancers: the elements of a puzzle
title_full_unstemmed From adjacent activation in Escherichia coli and DNA cyclization to eukaryotic enhancers: the elements of a puzzle
title_short From adjacent activation in Escherichia coli and DNA cyclization to eukaryotic enhancers: the elements of a puzzle
title_sort from adjacent activation in escherichia coli and dna cyclization to eukaryotic enhancers: the elements of a puzzle
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4217526/
https://www.ncbi.nlm.nih.gov/pubmed/25404937
http://dx.doi.org/10.3389/fgene.2014.00371
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