Evidence map›Paper›PMID 31392336›Full record

ArticleNucleic acids research2019

Engineering DNA recognition and allosteric response properties of TetR family proteins by using a module-swapping strategy.

Rey P Dimas, Benjamin R Jordan, Xian-Li Jiang, Catherine Martini, Joseph S Glavy, Dustin P Patterson, Faruck Morcos, Clement T Y Chan

Abstract read
In one paragraph

Article in Nucleic acids research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Programming Next-Generation Synthetic Biosensors by Genetic Circuit Design.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Transcription Factors as Evolvable Biosensors.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2021
    Review
  16. Review
  17. Review
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.

Rey P DimasDepartment of Biology, The University of Texas at Tyler, Tyler, TX 75799, USA.
Benjamin R JordanDepartment of Biology, The University of Texas at Tyler, Tyler, TX 75799, USA.
Xian-Li JiangDepartment of Biological Sciences, The University of Texas at Dallas, Richardson, TX 75080, USA.
Catherine MartiniDepartment of Biology, The University of Texas at Tyler, Tyler, TX 75799, USA.
Joseph S GlavyDepartment of Pharmaceutical Sciences, Fisch College of Pharmacy, The University of Texas at Tyler, Tyler, TX 75799, USA.
Dustin P PattersonDepartment of Chemistry and Biochemistry, The University of Texas at Tyler, Tyler, TX 75799, USA.
Faruck MorcosDepartment of Biological Sciences, The University of Texas at Dallas, Richardson, TX 75080, USA.
Clement T Y ChanDepartment of Biology, The University of Texas at Tyler, Tyler, TX 75799, USA.

Funding

Regulation of Pore Membrane Proteins during NPC Release and Dispersal in Open MitosisR15GM119118 · NIGMS · UNIVERSITY OF TEXAS TYLER · PI GLAVY, JOSEPH STEPHEN · 2016 to 2016
$394k
NIGMS NIH HHS R15 GM119118
6 · The paper itself

Abstract

The development of synthetic biological systems requires modular biomolecular components to flexibly alter response pathways. In previous studies, we have established a module-swapping design principle to engineer allosteric response and DNA recognition properties among regulators in the LacI family, in which the engineered regulators served as effective components for implementing new cellular behavior. Here we introduced this protein engineering strategy to two regulators in the TetR family: TetR (UniProt Accession ID: P04483) and MphR (Q9EVJ6). The TetR DNA-binding module and the MphR ligand-binding module were used to create the TetR-MphR. This resulting hybrid regulator possesses DNA-binding properties of TetR and ligand response properties of MphR, which is able to control gene expression in response to a molecular signal in cells. Furthermore, we studied molecular interactions between the TetR DNA-binding module and MphR ligand-binding module by using mutant analysis. Together, we demonstrated that TetR family regulators contain discrete and functional modules that can be used to build biological components with novel properties. This work highlights the utility of rational design as a means of creating modular parts for cell engineering and introduces new possibilities in rewiring cellular response pathways.

Indexed as

Protein EngineeringAllosteric RegulationBase SequenceBinding SitesCloning, MolecularCrystallography, X-RayDNAEscherichia coliEscherichia coli ProteinsGene ExpressionGenetic VectorsKineticsModels, MolecularMutationNucleic Acid ConformationProtein BindingDNAEscherichia coli ProteinsMphR(A) protein, E coliRecombinant Fusion ProteinsRepressor Proteinstetracycline resistance-encoding transposon repressor proteinTranscription Factors

Identifiers

PMID31392336
PMCPMC6895282

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.