Evidence map›Paper›PMID 26145755›Full record

ArticleNature communications2015

Concentration- and chromosome-organization-dependent regulator unbinding from DNA for transcription regulation in living cells.

Tai-Yen Chen, Ace George Santiago, Won Jung, Łukasz Krzemiński, Feng Yang, Danya J Martell, John D Helmann, Peng Chen

Abstract read
In one paragraph

Article in Nature communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing 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

69 citing papers in PubMed.

  1. Article
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  10. Memory effects of transcription regulator-DNA interactions in bacteria.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  11. Review
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  15. Article
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9 more citing papers are in PubMed but not listed here.

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

8 authors.

Tai-Yen ChenDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14853, USA.
Ace George SantiagoDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14853, USA.
Won JungDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14853, USA.
Łukasz KrzemińskiDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14853, USA.
Feng YangDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14853, USA.
Danya J MartellDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14853, USA.
John D HelmannDepartment of Microbiology, Cornell University, Ithaca, New York 14853, USA.
Peng ChenDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14853, USA.

Funding

CHEMISTRY OF BIOLOGICAL SYSTEMST32GM008500 · NIGMS · CORNELL UNIVERSITY ITHACA · PI LIN, HENING · 1996 to 2020
$5.4M
Zinc Homeostasis in Bacillus subtilisR01GM059323 · NIGMS · CORNELL UNIVERSITY ITHACA · PI HELMANN, JOHN D · 2000 to 2017
$4.5M
Unusual mechanisms of metal regulation in bacteria: from single molecules to single cells to cell communitiesR01GM109993 · NIGMS · CORNELL UNIVERSITY · PI Peng Chen · 2014 to 2026
$3.9M
Single Molecule Optically Resonant NanoTweezers for the study of Intracellular MeR01GM106420 · NIGMS · CORNELL UNIVERSITY · PI ERICKSON, DAVID CARL · 2013 to 2016
$1.1M
Single-molecule Imaging of Tripartite Membrane Efflux Pumps in Live BacteriaR21AI117295 · NIAID · CORNELL UNIVERSITY · PI CHEN, PENG · 2015 to 2016
$440k
NIAID NIH HHS AI117295NIAID NIH HHS R21 AI117295NIGMS NIH HHS GM106420NIGMS NIH HHS GM109993NIGMS NIH HHS R01 GM059323NIGMS NIH HHS R01 GM106420NIGMS NIH HHS R01 GM109993NIGMS NIH HHS T32 GM008500
6 · The paper itself

Abstract

Binding and unbinding of transcription regulators at operator sites constitute a primary mechanism for gene regulation. While many cellular factors are known to regulate their binding, little is known on how cells can modulate their unbinding for regulation. Using nanometer-precision single-molecule tracking, we study the unbinding kinetics from DNA of two metal-sensing transcription regulators in living Escherichia coli cells. We find that they show unusual concentration-dependent unbinding kinetics from chromosomal recognition sites in both their apo and holo forms. Unexpectedly, their unbinding kinetics further varies with the extent of chromosome condensation, and more surprisingly, varies in opposite ways for their apo-repressor versus holo-activator forms. These findings suggest likely broadly relevant mechanisms for facile switching between transcription activation and deactivation in vivo and in coordinating transcription regulation of resistance genes with the cell cycle.

Indexed as

Chromosomes, BacterialDNA, BacterialEscherichia coliEscherichia coli ProteinsGene Expression Regulation, BacterialNucleic Acid ConformationProtein BindingTranscription, GeneticDNA, BacterialEscherichia coli Proteins

Identifiers

PMID26145755
PMCPMC4507017

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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.