Evidence map›Paper›PMID 17205140›Full record

ArticlePloS one2006

Analysis of in-vivo LacR-mediated gene repression based on the mechanics of DNA looping.

Yongli Zhang, Abbye E McEwen, Donald M Crothers, Stephen D Levene

Abstract read
In one paragraph

Article in PloS one, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

41 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. High-resolution mapping of architectural DNA binding protein facilitation of a DNA repression loop in Escherichia coli.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  9. Article
  10. DNA topology confers sequence specificity to nonspecific architectural proteins.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  11. Article
  12. What controls DNA looping?International journal of molecular sciences · 2014
    Article
  13. Article
  14. Quantitation of the DNA tethering effect in long-range DNA looping in vivo and in vitro using the Lac and λ repressors.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Yongli ZhangDepartments of Chemistry and Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut, United States of America. ylzhang@lbl.gov
Abbye E McEwen
Donald M Crothers
Stephen D Levene

Funding

Nucleic Acid Structure, Dynamics and Protein InteractionR01GM021966 · NIGMS · YALE UNIVERSITY · PI CROTHERS, DONALD M · 1985 to 2009
$3.6M
Tangle Analysis of DNA Recombinases &Related ProteinsR01GM067242 · NIGMS · UNIVERSITY OF TEXAS DALLAS · PI DARCY, ISABEL K · 2002 to 2005
$1.2M
NUCLEIC ACID STRUCTURE AND PROTEIN INTERACTIONSR37GM021966 · NIGMS · YALE UNIVERSITY · PI CROTHERS, DONALD M · 1992 to 2001
$958k
NIGMS NIH HHS GM 21966NIGMS NIH HHS GM 67242NIGMS NIH HHS R01 GM021966NIGMS NIH HHS R01 GM067242NIGMS NIH HHS R37 GM021966
6 · The paper itself

Abstract

Interactions of E. coli lac repressor (LacR) with a pair of operator sites on the same DNA molecule can lead to the formation of looped nucleoprotein complexes both in vitro and in vivo. As a major paradigm for loop-mediated gene regulation, parameters such as operator affinity and spacing, repressor concentration, and DNA bending induced by specific or non-specific DNA-binding proteins (e.g., HU), have been examined extensively. However, a complete and rigorous model that integrates all of these aspects in a systematic and quantitative treatment of experimental data has not been available. Applying our recent statistical-mechanical theory for DNA looping, we calculated repression as a function of operator spacing (58-156 bp) from first principles and obtained excellent agreement with independent sets of in-vivo data. The results suggest that a linear extended, as opposed to a closed v-shaped, LacR conformation is the dominant form of the tetramer in vivo. Moreover, loop-mediated repression in wild-type E. coli strains is facilitated by decreased DNA rigidity and high levels of flexibility in the LacR tetramer. In contrast, repression data for strains lacking HU gave a near-normal value of the DNA persistence length. These findings underscore the importance of both protein conformation and elasticity in the formation of small DNA loops widely observed in vivo, and demonstrate the utility of quantitatively analyzing gene regulation based on the mechanics of nucleoprotein complexes.

Indexed as

Base SequenceBinding SitesBiomechanical PhenomenaDNA, BacterialEscherichia coliEscherichia coli ProteinsGene Expression Regulation, BacterialGenes, BacterialLac OperonLac RepressorsModels, MolecularNucleic Acid ConformationProtein ConformationProtein Structure, QuaternaryThermodynamicsDNA, BacterialEscherichia coli ProteinsLacI protein, E coliLac Repressors

Identifiers

PMID17205140
PMCPMC1762422

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.