Evidence map›Paper›PMID 22949686›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2012

Direct substitution and assisted dissociation pathways for turning off transcription by a MerR-family metalloregulator.

Chandra P Joshi, Debashis Panda, Danya J Martell, Nesha May Andoy, Tai-Yen Chen, Ahmed Gaballa, John D Helmann, Peng Chen

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing 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

53 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. The Copper Efflux Regulator (CueR).Sub-cellular biochemistry · 2024
    Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Unique underlying principles shaping copper homeostasis networks.Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry · 2022
    Review
  11. Article
  12. Article
  13. Review
  14. 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

8 authors.

Chandra P JoshiDepartments of Chemistry and Chemical Biology, Cornell University, Ithaca, NY 14853, USA.
Debashis Panda
Danya J Martell
Nesha May Andoy
Tai-Yen Chen
Ahmed Gaballa
John D Helmann
Peng Chen

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
Single-Molecule Study of Dynamics and Mechanisms of Biomacromolecule InteractionsR01GM082939 · NIGMS · CORNELL UNIVERSITY · PI CHEN, PENG · 2008 to 2012
$1.3M
NIGMS NIH HHS 5T32GM008500NIGMS NIH HHS GM059323NIGMS NIH HHS GM082939NIGMS NIH HHS R01 GM059323NIGMS NIH HHS R01 GM082939NIGMS NIH HHS T32 GM008500
6 · The paper itself

Abstract

Metalloregulators regulate transcription in response to metal ions. Many studies have provided insights into how transcription is activated upon metal binding by MerR-family metalloregulators. In contrast, how transcription is turned off after activation is unclear. Turning off transcription promptly is important, however, as the cells would not want to continue expressing metal resistance genes and thus waste energy after metal stress is relieved. Using single-molecule FRET measurements we studied the dynamic interactions of the copper efflux regulator (CueR), a Cu(+)-responsive MerR-family metalloregulator, with DNA. Besides quantifying its DNA binding and unbinding kinetics, we discovered that CueR spontaneously flips its binding orientation at the recognition site. CueR also has two different binding modes, corresponding to interactions with specific and nonspecific DNA sequences, which would facilitate recognition localization. Most strikingly, a CueR molecule coming from solution can directly substitute for a DNA-bound CueR or assist the dissociation of the incumbent CueR, both of which are unique examples for any DNA-binding protein. The kinetics of the direct protein substitution and assisted dissociation reactions indicate that these two unique processes can provide efficient pathways to replace a DNA-bound holo-CueR with apo-CueR, thus turning off transcription promptly and facilely.

Indexed as

Bacterial Physiological PhenomenaBacterial ProteinsDNADNA-Binding ProteinsEscherichia coliFluorescence Resonance Energy TransferIonsKineticsMetalsModels, BiologicalProtein BindingSulfhydryl CompoundsTranscription, GeneticBacterial ProteinsDNADNA-Binding ProteinsIonsMerR protein, BacteriaMetalsSulfhydryl Compounds

Identifiers

PMID22949686
PMCPMC3458356

What OpenQuestion holds

Textmetadata
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.