Evidence map›Paper›PMID 25979263›Full record

ArticleNucleic acids research2015

De novo design of heat-repressible RNA thermosensors in E. coli.

Allison Hoynes-O'Connor, Kristina Hinman, Lukas Kirchner, Tae Seok Moon

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
4.1field-weighted citation impact, top 6% of its field
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

22 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
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  8. Cybergenetic control of microbial community composition.Frontiers in bioengineering and biotechnology · 2022
    Review
  9. Article
  10. Biosensing in Smart Engineered Probiotics.Biotechnology journal · 2020
    Review
  11. Article
  12. Review
  13. Biomolecular Ultrasound and Sonogenetics.Annual review of chemical and biomolecular engineering · 2018
    Review
  14. RNA Thermometers for the PURExpress System.ACS synthetic biology · 2018
    Article
  15. Article
  16. Article
  17. Article
  18. Article
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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

4 authors at 1 institution in 1 country.

Allison Hoynes-O'ConnorEnergy, Environmental and Chemical Engineering, Washington University in St. Louis, St. Louis, MO 63130, USA.
Kristina HinmanEnergy, Environmental and Chemical Engineering, Washington University in St. Louis, St. Louis, MO 63130, USA.
Lukas KirchnerEnergy, Environmental and Chemical Engineering, Washington University in St. Louis, St. Louis, MO 63130, USA.
Tae Seok MoonEnergy, Environmental and Chemical Engineering, Washington University in St. Louis, St. Louis, MO 63130, USA tsmoon@wustl.edu.ORCID http://orcid.org/0000-0001-8373-9051
Washington University in St. Louis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RNA-based temperature sensing is common in bacteria that live in fluctuating environments. Most naturally-occurring RNA thermosensors are heat-inducible, have long sequences, and function by sequestering the ribosome binding site in a hairpin structure at lower temperatures. Here, we demonstrate the de novo design of short, heat-repressible RNA thermosensors. These thermosensors contain a cleavage site for RNase E, an enzyme native to Escherichia coli and many other organisms, in the 5' untranslated region of the target gene. At low temperatures, the cleavage site is sequestered in a stem-loop, and gene expression is unobstructed. At high temperatures, the stem-loop unfolds, allowing for mRNA degradation and turning off expression. We demonstrated that these thermosensors respond specifically to temperature and provided experimental support for the central role of RNase E in the mechanism. We also demonstrated the modularity of these RNA thermosensors by constructing a three-input composite circuit that utilizes transcriptional, post-transcriptional, and post-translational regulation. A thorough analysis of the 24 thermosensors allowed for the development of design guidelines for systematic construction of similar thermosensors in future applications. These short, modular RNA thermosensors can be applied to the construction of complex genetic circuits, facilitating rational reprogramming of cellular processes for synthetic biology applications.

Indexed as

Gene Expression Regulation, BacterialHot TemperatureEndoribonucleasesEscherichia coliProtein BiosynthesisTranscription, GeneticEndoribonucleasesribonuclease E

Identifiers

PMID25979263
PMCPMC4499127
OpenAlexW1791348914

What OpenQuestion holds

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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.