Evidence map›Paper›PMID 26837577›Full record

ArticleNucleic acids research2016

Programmable control of bacterial gene expression with the combined CRISPR and antisense RNA system.

Young Je Lee, Allison Hoynes-O'Connor, Matthew C Leong, Tae Seok Moon

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
8.7field-weighted citation impact, top 2% 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

52 citing papers in PubMed, 117 citations in OpenAlex.

  1. Article
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  4. Design of CRISPRi-Based Synthetic Gene Circuits in Bacteria.Methods in molecular biology (Clifton, N.J.) · 2026
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  14. CRISPR-based screening of small RNA modulators of bile susceptibility inProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Isobutanol production by combinedMetabolic engineering communications · 2022
    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

4 authors at 1 institution in 1 country.

Young Je LeeDepartment of Energy, Environmental and Chemical Engineering, Washington University in St. Louis, St. Louis, MO, USA.
Allison Hoynes-O'ConnorDepartment of Energy, Environmental and Chemical Engineering, Washington University in St. Louis, St. Louis, MO, USA.
Matthew C LeongDepartment of Energy, Environmental and Chemical Engineering, Washington University in St. Louis, St. Louis, MO, USA.
Tae Seok MoonDepartment of Energy, Environmental and Chemical Engineering, Washington University in St. Louis, St. Louis, MO, 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

A central goal of synthetic biology is to implement diverse cellular functions by predictably controlling gene expression. Though research has focused more on protein regulators than RNA regulators, recent advances in our understanding of RNA folding and functions have motivated the use of RNA regulators. RNA regulators provide an advantage because they are easier to design and engineer than protein regulators, potentially have a lower burden on the cell and are highly orthogonal. Here, we combine the CRISPR system from Streptococcus pyogenes and synthetic antisense RNAs (asRNAs) in Escherichia coli strains to repress or derepress a target gene in a programmable manner. Specifically, we demonstrate for the first time that the gene target repressed by the CRISPR system can be derepressed by expressing an asRNA that sequesters a small guide RNA (sgRNA). Furthermore, we demonstrate that tunable levels of derepression can be achieved (up to 95%) by designing asRNAs that target different regions of a sgRNA and by altering the hybridization free energy of the sgRNA-asRNA complex. This new system, which we call the combined CRISPR and asRNA system, can be used to reversibly repress or derepress multiple target genes simultaneously, allowing for rational reprogramming of cellular functions.

Indexed as

Clustered Regularly Interspaced Short Palindromic RepeatsGene Expression Regulation, BacterialDrug DesignEscherichia coliGenes, ReporterGene TargetingGreen Fluorescent ProteinsNucleic Acid HybridizationPlasmidsRNA, AntisenseRNA, Guide, CRISPR-Cas SystemsStreptococcus pyogenesGreen Fluorescent ProteinsRNA, AntisenseRNA, Guide, CRISPR-Cas Systems

Identifiers

PMID26837577
PMCPMC4797300
OpenAlexW2268557312

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.