Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/89375
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Type: Journal article
Title: Quantitation of the DNA tethering effect in long-range DNA looping in vivo and in vitro using the Lac and λ repressors
Other Titles: Quantitation of the DNA tethering effect in long-range DNA looping in vivo and in vitro using the Lac and lambda repressors
Author: Priest, D.G.
Cui, L.
Kumar, S.
Dunlap, D.D.
Dodd, I.B.
Shearwin, K.E.
Citation: Proceedings of the National Academy of Sciences USA, 2014; 111(1):349-354
Publisher: National Academy of Sciences
Issue Date: 2014
ISSN: 0027-8424
1091-6490
Statement of
Responsibility: 
David G. Priest, Lun Cui, Sandip Kumar, David D. Dunlap, Ian B. Dodd and Keith E. Shearwin
Abstract: Efficient and specific interactions between proteins bound to the same DNA molecule can be dependent on the length of the DNA tether that connects them. Measurement of the strength of this DNA tethering effect has been largely confined to short separations between sites, and it is not clear how it contributes to long-range DNA looping interactions, such as occur over separations of tens to hundreds of kilobase pairs in vivo. Here, gene regulation experiments using the LacI and λ CI repressors, combined with mathematical modeling, were used to quantitate DNA tethering inside Escherichia coli cells over the 250- to 10,000-bp range. Although LacI and CI loop DNA in distinct ways, measurements of the tethering effect were very similar for both proteins. Tethering strength decreased with increasing separation, but even at 5- to 10-kb distances, was able to increase contact probability 10- to 20-fold and drive efficient looping. Tethering in vitro with the Lac repressor was measured for the same 600-to 3,200-bp DNAs using tethered particle motion, a single molecule technique, and was 5- to 45-fold weaker than in vivo over this range. Thus, the enhancement of looping seen previously in vivo at separations below 500 bp extends to large separations, underlining the need to understand how in vivo factors aid DNA looping. Our analysis also suggests how efficient and specific looping could be achieved over very long DNA separations, such as what occurs between enhancers and promoters in eukaryotic cells
Keywords: Escherichia coli; Escherichia coli Proteins; Repressor Proteins; DNA, Bacterial; Protein Interaction Mapping; Gene Expression Regulation; Lac Operon; Genes, Reporter; Algorithms; Thermodynamics; Models, Theoretical; Time Factors; Viral Regulatory and Accessory Proteins; Enhancer Elements, Genetic; Promoter Regions, Genetic; Lac Repressors
Rights: © 2014 National Academy of Sciences
RMID: 0020134525
DOI: 10.1073/pnas.1317817111
Grant ID: http://purl.org/au-research/grants/arc/DP110100824
http://purl.org/au-research/grants/arc/DP110101470
http://purl.org/au-research/grants/nhmrc/1025549
Appears in Collections:Molecular and Biomedical Science publications

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