Evidence map›Paper›PMID 29302024›Full record

ArticleNature communications2018

Tuning the dynamic range of bacterial promoters regulated by ligand-inducible transcription factors.

Ye Chen, Joanne M L Ho, David L Shis, Chinmaya Gupta, James Long, Daniel S Wagner, William Ott, Krešimir Josić, Matthew R Bennett

Abstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 86 papers.

0numbers the graph read from it
0cells of the map it votes in
86citing 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

86 citing papers in PubMed.

  1. Review
  2. Optimized cumate toolkit for tunable protein expression duringApplied and environmental microbiology · 2026
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  7. Programming Next-Generation Synthetic Biosensors by Genetic Circuit Design.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Science (New York, N.Y.) · 2025
    Article
  17. Article
  18. Article
  19. Why cellular computations challenge our design principles.Seminars in cell & developmental biology · 2025
    Review
  20. Article

26 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

9 authors.

Ye ChenDepartment of Biosciences, Rice University, 6100 Main Street, Houston, TX, 77005, USA.ORCID http://orcid.org/0000-0003-1247-5444
Joanne M L HoDepartment of Biosciences, Rice University, 6100 Main Street, Houston, TX, 77005, USA.
David L ShisDepartment of Biosciences, Rice University, 6100 Main Street, Houston, TX, 77005, USA.
Chinmaya GuptaDepartment of Mathematics, University of Houston, 4800 Calhoun Road, Houston, TX, 77204, USA.
James LongDepartment of Biosciences, Rice University, 6100 Main Street, Houston, TX, 77005, USA.
Daniel S WagnerDepartment of Biosciences, Rice University, 6100 Main Street, Houston, TX, 77005, USA.
William OttDepartment of Mathematics, University of Houston, 4800 Calhoun Road, Houston, TX, 77204, USA.
Krešimir JosićDepartment of Biosciences, Rice University, 6100 Main Street, Houston, TX, 77005, USA. josic@math.uh.edu.
Matthew R BennettDepartment of Biosciences, Rice University, 6100 Main Street, Houston, TX, 77005, USA. matthew.bennett@rice.edu.

Funding

Expanding the utility of transcriptional bacterial computingR01GM117138 · NIGMS · RICE UNIVERSITY · PI BENNETT, MATTHEW R., JOSIC, KRESIMIR · 2016 to 2019
$2.0M
Experimental and mathematical analysis of delay in transcripitional signalingR01GM104974 · NIGMS · RICE UNIVERSITY · PI BENNETT, MATTHEW R. · 2012 to 2016
$1.4M
NIGMS NIH HHS R01 GM104974NIGMS NIH HHS R01 GM117138
6 · The paper itself

Abstract

One challenge for synthetic biologists is the predictable tuning of genetic circuit regulatory components to elicit desired outputs. Gene expression driven by ligand-inducible transcription factor systems must exhibit the correct ON and OFF characteristics: appropriate activation and leakiness in the presence and absence of inducer, respectively. However, the dynamic range of a promoter (i.e., absolute difference between ON and OFF states) is difficult to control. We report a method that tunes the dynamic range of ligand-inducible promoters to achieve desired ON and OFF characteristics. We build combinatorial sets of AraC-and LasR-regulated promoters containing -10 and -35 sites from synthetic and Escherichia coli promoters. Four sequence combinations with diverse dynamic ranges were chosen to build multi-input transcriptional logic gates regulated by two and three ligand-inducible transcription factors (LacI, TetR, AraC, XylS, RhlR, LasR, and LuxR). This work enables predictable control over the dynamic range of regulatory components.

Indexed as

Gene Expression Regulation, BacterialAlgorithmsEscherichia coliEscherichia coli ProteinsLigandsModels, GeneticPromoter Regions, GeneticThermodynamicsTranscription FactorsTranscription, GeneticEscherichia coli ProteinsLigandsTranscription Factors

Identifiers

PMID29302024
PMCPMC5754348

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.