Evidence map›Paper›PMID 24169405›Full record

ArticleMolecular systems biology2013

Design of orthogonal genetic switches based on a crosstalk map of σs, anti-σs, and promoters.

Virgil A Rhodius, Thomas H Segall-Shapiro, Brian D Sharon, Amar Ghodasara, Ekaterina Orlova, Hannah Tabakh, David H Burkhardt, Kevin Clancy, Todd C Peterson, Carol A Gross and 1 more

Abstract read
In one paragraph

Article in Molecular systems biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 100 papers.

0numbers the graph read from it
0cells of the map it votes in
100citing 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

100 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Gene circuit-based sensors.Fundamental research · 2025
    Review
  7. ACS synthetic biology · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. START: A Versatile Platform for Bacterial Ligand Sensing with Programmable Performances.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  17. Article
  18. Article
  19. Article
  20. Article

40 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

11 authors.

Virgil A RhodiusDepartment of Microbiology and Immunology, University of California San Francisco, San Francisco, CA, USA.
Thomas H Segall-Shapiro
Brian D Sharon
Amar Ghodasara
Ekaterina Orlova
Hannah Tabakh
David H Burkhardt
Kevin Clancy
Todd C Peterson
Carol A Gross
Christopher A Voigt

Funding

STRUCTURAL BIOLOGY TRAINING PROGRAMT32GM008284 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KORTEMME, TANJA · 1988 to 2022
$10.1M
MUTATIONAL ANALYSIS OF E COLI CORE RNA POLYMERASER01GM057755 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GROSS, CAROL ANNE · 1998 to 2013
$6.2M
REGULATION OF THE HEAT-SHOCK RESPONSE IN E COLIR01GM036278 · NIGMS · UNIVERSITY OF WISCONSIN MADISON · PI GROSS, CAROL ANNE · 1986 to 2016
$5.2M
Integrative Program in Complex Biological System (ipCBS)T32EB009383 · NIBIB · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MARSHALL, WALLACE, WEINER, ORION D · 2009 to 2022
$3.2M
System Dynamics of the Salmonella Virulence Regulatory NetworkR01AI067699 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI VOIGT, CHRISTOPHER A · 2007 to 2011
$1.5M
System Dynamics of the Salmonella Virulence Regulatory NetworkR56AI067699 · NIAID · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI VOIGT, CHRISTOPHER A · 2012 to 2012
$279k
NIAID NIH HHS NIH AI067699NIAID NIH HHS R01 AI067699NIAID NIH HHS R56 AI067699NIBIB NIH HHS T32 EB009383NIGMS NIH HHS NIH R01GM057755-31NIGMS NIH HHS NIH T32GM008284NIGMS NIH HHS R01 GM036278NIGMS NIH HHS R01 GM057755NIGMS NIH HHS T32 GM008284
6 · The paper itself

Abstract

Cells react to their environment through gene regulatory networks. Network integrity requires minimization of undesired crosstalk between their biomolecules. Similar constraints also limit the use of regulators when building synthetic circuits for engineering applications. Here, we mapped the promoter specificities of extracytoplasmic function (ECF) σs as well as the specificity of their interaction with anti-σs. DNA synthesis was used to build 86 ECF σs (two from every subgroup), their promoters, and 62 anti-σs identified from the genomes of diverse bacteria. A subset of 20 σs and promoters were found to be highly orthogonal to each other. This set can be increased by combining the -35 and -10 binding domains from different subgroups to build chimeras that target sequences unrepresented in any subgroup. The orthogonal σs, anti-σs, and promoters were used to build synthetic genetic switches in Escherichia coli. This represents a genome-scale resource of the properties of ECF σs and a resource for synthetic biology, where this set of well-characterized regulatory parts will enable the construction of sophisticated gene expression programs.

Indexed as

Gene Expression Regulation, BacterialGenes, SwitchPromoter Regions, GeneticData MiningEscherichia coliEscherichia coli ProteinsGenetic EngineeringModels, GeneticPhylogenyProtein BindingSigma FactorTranscription, GeneticelbB protein, E coliEscherichia coli ProteinsSigma Factor

Identifiers

PMID24169405
PMCPMC3817407

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.