Evidence map›Paper›PMID 21195233›Full record

ArticleMethods in enzymology2011

Quantitative methods for measuring DNA flexibility in vitro and in vivo.

Justin P Peters, Nicole A Becker, Emily M Rueter, Zeljko Bajzer, Jason D Kahn, L James Maher

Abstract read
In one paragraph

Article in Methods in enzymology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.4field-weighted citation impact, top 7% of its field
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

25 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. High-Resolution Characterization of DNA/Protein Complexes in Living Bacteria.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Dependence of DNA looping onInternational journal of biochemistry and molecular biology · 2019
    Article
  11. Article
  12. Article
  13. Using synthetic biology to make cells tomorrow's test tubes.Integrative biology : quantitative biosciences from nano to macro · 2016
    Review
  14. Article
  15. Article
  16. 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
  17. Article
  18. Article
  19. Mechanical properties of DNA-like polymers.Nucleic acids research · 2013
    Article
  20. Molecular basis for sequence-dependent induced DNA bending.Chembiochem : a European journal of chemical biology · 2013
    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

6 authors at 2 institutions in 1 country.

Justin P PetersDepartment of Biochemistry and Molecular Biology, Mayo Clinic College of Medicine, Rochester, Minnesota, USA.
Nicole A Becker
Emily M Rueter
Zeljko Bajzer
Jason D Kahn
L James Maher
Mayo Clinic · USUniversity of Maryland, College Park · US

Funding

Enhancement of Cellular DNA FlexibilityR01GM075965 · NIGMS · MAYO CLINIC ROCHESTER · PI MAHER, LOUIS JAMES · 2006 to 2018
$4.2M
DNA Topology In TBP/DNA Complexes: Chromatin ConnectionsR01GM053620 · NIGMS · UNIVERSITY OF MARYLAND COLLEGE PK CAMPUS · PI KAHN, JASON D · 1997 to 2004
$918k
ELECTROSTATIC FORCES IN DNA BENDING BY PROTEINSR01GM054411 · NIGMS · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI MAHER, LOUIS JAMES · 1995 to 2003
$846k
NIGMS NIH HHS GM075965NIGMS NIH HHS GM53620NIGMS NIH HHS GM54411NIGMS NIH HHS R01 GM053620NIGMS NIH HHS R01 GM054411NIGMS NIH HHS R01 GM075965
6 · The paper itself

Abstract

The double-helical DNA biopolymer is particularly resistant to bending and twisting deformations. This property has important implications for DNA folding in vitro and for the packaging and function of DNA in living cells. Among the outstanding questions in the field of DNA biophysics are the underlying origin of DNA stiffness and the mechanisms by which DNA stiffness is overcome within cells. Exploring these questions requires experimental methods to quantitatively measure DNA bending and twisting stiffness both in vitro and in vivo. Here, we discuss two classical approaches: T4 DNA ligase-mediated DNA cyclization kinetics and lac repressor-mediated DNA looping in Escherichia coli. We review the theoretical basis for these techniques and how each can be applied to quantitate biophysical parameters that describe the DNA polymer. We then show how we have modified these methods and applied them to quantitate how apparent DNA physical properties are altered in vitro and in vivo by sequence-nonspecific architectural DNA-binding proteins such as the E. coli HU protein and eukaryotic HMGB proteins.

Indexed as

Nucleic Acid ConformationOperator Regions, GeneticAmino Acid SequenceBase SequenceCarrier ProteinsCyclizationDNA, BacterialDNA-Binding ProteinsDNA, CircularDNA LigasesEnzyme AssaysEscherichia coli ProteinsGene DeletionHMGB ProteinsKineticsLac OperonCarrier ProteinsDNA, BacterialDNA-Binding ProteinsDNA, CircularDNA LigasesEscherichia coli ProteinsHMGB ProteinshupA protein, E coliHupB protein, E coliLac RepressorsTranscription Factors

Identifiers

PMID21195233
PMCPMC4190681
OpenAlexW1825951756

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.