What Controls DNA Looping?

The looping of DNA provides a means of communication between sequentially distant genomic sites that operate in tandem to express, copy, and repair the information encoded in the DNA base sequence. The short loops implicated in the expression of bacterial genes suggest that molecular factors other t...

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Main Authors: Pamela J. Perez, Nicolas Clauvelin, Michael A. Grosner, Andrew V. Colasanti, Wilma K. Olson
Format: Article
Language:English
Published: MDPI AG 2014-08-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:http://www.mdpi.com/1422-0067/15/9/15090
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spelling doaj-f0b18c0827c84785a24a5935e5dc3f4d2020-11-25T00:15:13ZengMDPI AGInternational Journal of Molecular Sciences1422-00672014-08-01159150901510810.3390/ijms150915090ijms150915090What Controls DNA Looping?Pamela J. Perez0Nicolas Clauvelin1Michael A. Grosner2Andrew V. Colasanti3Wilma K. Olson4BioMaPS Institute for Quantitative Biology, Rutgers, the State University of New Jersey, Piscataway, NJ 08854, USABioMaPS Institute for Quantitative Biology, Rutgers, the State University of New Jersey, Piscataway, NJ 08854, USABioMaPS Institute for Quantitative Biology, Rutgers, the State University of New Jersey, Piscataway, NJ 08854, USABioMaPS Institute for Quantitative Biology, Rutgers, the State University of New Jersey, Piscataway, NJ 08854, USABioMaPS Institute for Quantitative Biology, Rutgers, the State University of New Jersey, Piscataway, NJ 08854, USAThe looping of DNA provides a means of communication between sequentially distant genomic sites that operate in tandem to express, copy, and repair the information encoded in the DNA base sequence. The short loops implicated in the expression of bacterial genes suggest that molecular factors other than the naturally stiff double helix are involved in bringing the interacting sites into close spatial proximity. New computational techniques that take direct account of the three-dimensional structures and fluctuations of protein and DNA allow us to examine the likely means of enhancing such communication. Here, we describe the application of these approaches to the looping of a 92 base-pair DNA segment between the headpieces of the tetrameric Escherichia coli Lac repressor protein. The distortions of the double helix induced by a second protein—the nonspecific nucleoid protein HU—increase the computed likelihood of looping by several orders of magnitude over that of DNA alone. Large-scale deformations of the repressor, sequence-dependent features in the DNA loop, and deformability of the DNA operators also enhance looping, although to lesser degrees. The correspondence between the predicted looping propensities and the ease of looping derived from gene-expression and single-molecule measurements lends credence to the derived structural picture.http://www.mdpi.com/1422-0067/15/9/15090DNA loopingoptimizationJ factorlac operonMonte Carlo simulations
collection DOAJ
language English
format Article
sources DOAJ
author Pamela J. Perez
Nicolas Clauvelin
Michael A. Grosner
Andrew V. Colasanti
Wilma K. Olson
spellingShingle Pamela J. Perez
Nicolas Clauvelin
Michael A. Grosner
Andrew V. Colasanti
Wilma K. Olson
What Controls DNA Looping?
International Journal of Molecular Sciences
DNA looping
optimization
J factor
lac operon
Monte Carlo simulations
author_facet Pamela J. Perez
Nicolas Clauvelin
Michael A. Grosner
Andrew V. Colasanti
Wilma K. Olson
author_sort Pamela J. Perez
title What Controls DNA Looping?
title_short What Controls DNA Looping?
title_full What Controls DNA Looping?
title_fullStr What Controls DNA Looping?
title_full_unstemmed What Controls DNA Looping?
title_sort what controls dna looping?
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2014-08-01
description The looping of DNA provides a means of communication between sequentially distant genomic sites that operate in tandem to express, copy, and repair the information encoded in the DNA base sequence. The short loops implicated in the expression of bacterial genes suggest that molecular factors other than the naturally stiff double helix are involved in bringing the interacting sites into close spatial proximity. New computational techniques that take direct account of the three-dimensional structures and fluctuations of protein and DNA allow us to examine the likely means of enhancing such communication. Here, we describe the application of these approaches to the looping of a 92 base-pair DNA segment between the headpieces of the tetrameric Escherichia coli Lac repressor protein. The distortions of the double helix induced by a second protein—the nonspecific nucleoid protein HU—increase the computed likelihood of looping by several orders of magnitude over that of DNA alone. Large-scale deformations of the repressor, sequence-dependent features in the DNA loop, and deformability of the DNA operators also enhance looping, although to lesser degrees. The correspondence between the predicted looping propensities and the ease of looping derived from gene-expression and single-molecule measurements lends credence to the derived structural picture.
topic DNA looping
optimization
J factor
lac operon
Monte Carlo simulations
url http://www.mdpi.com/1422-0067/15/9/15090
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