Evidence map›Paper›PMID 32609820›Full record

ArticleNucleic acids research2020

Toward a translationally independent RNA-based synthetic oscillator using deactivated CRISPR-Cas.

James Kuo, Ruoshi Yuan, Carlos Sánchez, Johan Paulsson, Pamela A Silver

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

21 citing papers in PubMed, 33 citations in OpenAlex.

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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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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

5 authors at 2 institutions in 1 country.

James KuoDepartment of Systems Biology, Blavatnik Institute at Harvard Medical School, Boston, MA 02115, USA.
Ruoshi YuanDepartment of Systems Biology, Blavatnik Institute at Harvard Medical School, Boston, MA 02115, USA.
Carlos SánchezDepartment of Systems Biology, Blavatnik Institute at Harvard Medical School, Boston, MA 02115, USA.
Johan PaulssonDepartment of Systems Biology, Blavatnik Institute at Harvard Medical School, Boston, MA 02115, USA.
Pamela A SilverDepartment of Systems Biology, Blavatnik Institute at Harvard Medical School, Boston, MA 02115, USA.
Harvard University · USBoston VA Research Institute · US

Funding

A synchronized circadian clock in gut bacteria, using control theoryF32GM125108 · NIGMS · HARVARD MEDICAL SCHOOL · PI KUO, JAMES C. · 2017 to 2019
$179k
Defense Advanced Research Projects Agency HR0011-16-2-0049National Science Foundation 1517372National Science Foundation 1562497National Science Foundation 1615487NIGMS NIH HHS F32 GM125108
6 · The paper itself

Abstract

In synthetic circuits, CRISPR-Cas systems have been used effectively for endpoint changes from an initial state to a final state, such as in logic gates. Here, we use deactivated Cas9 (dCas9) and deactivated Cas12a (dCas12a) to construct dynamic RNA ring oscillators that cycle continuously between states over time in bacterial cells. While our dCas9 circuits using 103-nt guide RNAs showed irregular fluctuations with a wide distribution of peak-to-peak period lengths averaging approximately nine generations, a dCas12a oscillator design with 40-nt CRISPR RNAs performed much better, having a strongly repressed off-state, distinct autocorrelation function peaks, and an average peak-to-peak period length of ∼7.5 generations. Along with free-running oscillator circuits, we measure repression response times in open-loop systems with inducible RNA steps to compare with oscillator period times. We track thousands of cells for 24+ h at the single-cell level using a microfluidic device. In creating a circuit with nearly translationally independent behavior, as the RNAs control each others' transcription, we present the possibility for a synthetic oscillator generalizable across many organisms and readily linkable for transcriptional control.

Indexed as

CRISPR-Cas SystemsPeriodicityBacterial ProteinsCRISPR-Associated Protein 9CRISPR-Associated ProteinsEndodeoxyribonucleasesEscherichia coliMicrofluidicsRNA, Guide, CRISPR-Cas SystemsSingle-Cell AnalysisBacterial ProteinsCas12a proteinCRISPR-Associated Protein 9CRISPR-Associated ProteinsEndodeoxyribonucleasesRNA, Guide, CRISPR-Cas Systems

Identifiers

PMID32609820
PMCPMC7430638
OpenAlexW3040184489

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.