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FRET studies of a landscape of Lac repressor-mediated DNA loops
DNA looping mediated by the Lac repressor is an archetypal test case for modeling protein and DNA flexibility. Understanding looping is fundamental to quantitative descriptions of gene expression. Systematic analysis of LacI•DNA looping was carried out using a landscape of DNA constructs with lac op...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3378866/ https://www.ncbi.nlm.nih.gov/pubmed/22307389 http://dx.doi.org/10.1093/nar/gks019 |
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author | Haeusler, Aaron R. Goodson, Kathy A. Lillian, Todd D. Wang, Xiaoyu Goyal, Sachin Perkins, Noel C. Kahn, Jason D. |
author_facet | Haeusler, Aaron R. Goodson, Kathy A. Lillian, Todd D. Wang, Xiaoyu Goyal, Sachin Perkins, Noel C. Kahn, Jason D. |
author_sort | Haeusler, Aaron R. |
collection | PubMed |
description | DNA looping mediated by the Lac repressor is an archetypal test case for modeling protein and DNA flexibility. Understanding looping is fundamental to quantitative descriptions of gene expression. Systematic analysis of LacI•DNA looping was carried out using a landscape of DNA constructs with lac operators bracketing an A-tract bend, produced by varying helical phasings between operators and the bend. Fluorophores positioned on either side of both operators allowed direct Förster resonance energy transfer (FRET) detection of parallel (P1) and antiparallel (A1, A2) DNA looping topologies anchored by V-shaped LacI. Combining fluorophore position variant landscapes allows calculation of the P1, A1 and A2 populations from FRET efficiencies and also reveals extended low-FRET loops proposed to form via LacI opening. The addition of isopropyl-β-d-thio-galactoside (IPTG) destabilizes but does not eliminate the loops, and IPTG does not redistribute loops among high-FRET topologies. In some cases, subsequent addition of excess LacI does not reduce FRET further, suggesting that IPTG stabilizes extended or other low-FRET loops. The data align well with rod mechanics models for the energetics of DNA looping topologies. At the peaks of the predicted energy landscape for V-shaped loops, the proposed extended loops are more stable and are observed instead, showing that future models must consider protein flexibility. |
format | Online Article Text |
id | pubmed-3378866 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-33788662012-06-20 FRET studies of a landscape of Lac repressor-mediated DNA loops Haeusler, Aaron R. Goodson, Kathy A. Lillian, Todd D. Wang, Xiaoyu Goyal, Sachin Perkins, Noel C. Kahn, Jason D. Nucleic Acids Res Gene Regulation, Chromatin and Epigenetics DNA looping mediated by the Lac repressor is an archetypal test case for modeling protein and DNA flexibility. Understanding looping is fundamental to quantitative descriptions of gene expression. Systematic analysis of LacI•DNA looping was carried out using a landscape of DNA constructs with lac operators bracketing an A-tract bend, produced by varying helical phasings between operators and the bend. Fluorophores positioned on either side of both operators allowed direct Förster resonance energy transfer (FRET) detection of parallel (P1) and antiparallel (A1, A2) DNA looping topologies anchored by V-shaped LacI. Combining fluorophore position variant landscapes allows calculation of the P1, A1 and A2 populations from FRET efficiencies and also reveals extended low-FRET loops proposed to form via LacI opening. The addition of isopropyl-β-d-thio-galactoside (IPTG) destabilizes but does not eliminate the loops, and IPTG does not redistribute loops among high-FRET topologies. In some cases, subsequent addition of excess LacI does not reduce FRET further, suggesting that IPTG stabilizes extended or other low-FRET loops. The data align well with rod mechanics models for the energetics of DNA looping topologies. At the peaks of the predicted energy landscape for V-shaped loops, the proposed extended loops are more stable and are observed instead, showing that future models must consider protein flexibility. Oxford University Press 2012-05 2012-02-04 /pmc/articles/PMC3378866/ /pubmed/22307389 http://dx.doi.org/10.1093/nar/gks019 Text en © The Author(s) 2012. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Gene Regulation, Chromatin and Epigenetics Haeusler, Aaron R. Goodson, Kathy A. Lillian, Todd D. Wang, Xiaoyu Goyal, Sachin Perkins, Noel C. Kahn, Jason D. FRET studies of a landscape of Lac repressor-mediated DNA loops |
title | FRET studies of a landscape of Lac repressor-mediated DNA loops |
title_full | FRET studies of a landscape of Lac repressor-mediated DNA loops |
title_fullStr | FRET studies of a landscape of Lac repressor-mediated DNA loops |
title_full_unstemmed | FRET studies of a landscape of Lac repressor-mediated DNA loops |
title_short | FRET studies of a landscape of Lac repressor-mediated DNA loops |
title_sort | fret studies of a landscape of lac repressor-mediated dna loops |
topic | Gene Regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3378866/ https://www.ncbi.nlm.nih.gov/pubmed/22307389 http://dx.doi.org/10.1093/nar/gks019 |
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