Evidence map›Paper›PMID 31904924›Full record

ArticleACS chemical biology2020

Heat-Triggered Remote Control of CRISPR-dCas9 for Tunable Transcriptional Modulation.

Lena Gamboa, Erick V Phung, Haoxin Li, Jared P Meyers, Anna C Hart, Ian C Miller, Gabriel A Kwong

Abstract read
In one paragraph

Article in ACS chemical biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

19 citing papers in PubMed, 37 citations in OpenAlex.

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  11. In vivo gene delivery to immune cells.Current opinion in biotechnology · 2024
    Review
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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

7 authors at 1 institution in 1 country.

Lena GamboaThe Wallace H. Coulter Department of Biomedical Engineering , Georgia Institute of Technology and Emory University , Atlanta , Georgia 30332 , United States.
Erick V PhungThe Wallace H. Coulter Department of Biomedical Engineering , Georgia Institute of Technology and Emory University , Atlanta , Georgia 30332 , United States.
Haoxin LiThe Wallace H. Coulter Department of Biomedical Engineering , Georgia Institute of Technology and Emory University , Atlanta , Georgia 30332 , United States.
Jared P MeyersThe Wallace H. Coulter Department of Biomedical Engineering , Georgia Institute of Technology and Emory University , Atlanta , Georgia 30332 , United States.
Anna C HartThe Wallace H. Coulter Department of Biomedical Engineering , Georgia Institute of Technology and Emory University , Atlanta , Georgia 30332 , United States.
Ian C MillerThe Wallace H. Coulter Department of Biomedical Engineering , Georgia Institute of Technology and Emory University , Atlanta , Georgia 30332 , United States.
Gabriel A KwongThe Wallace H. Coulter Department of Biomedical Engineering , Georgia Institute of Technology and Emory University , Atlanta , Georgia 30332 , United States.ORCID 0000-0002-6255-6755
Georgia Institute of Technology · US

Funding

Atlanta Clinical and Translational Science Institute (ACTSI) RenewalUL1TR000454 · NCATS · EMORY UNIVERSITY · PI STEPHENS, DAVID S · 2012 to 2016
$25.8M
Noninvasive and predictive biomarkers of organ transplant rejectionDP2HD091793 · NICHD · GEORGIA INSTITUTE OF TECHNOLOGY · PI KWONG, GABRIEL A · 2016 to 2016
$2.4M
Graduate Training for Rationally Designed, Integrative Biomaterials - GT BioMATT32EB006343 · NIBIB · GEORGIA INSTITUTE OF TECHNOLOGY · PI TEMENOFF, JOHNNA S · 2008 to 2018
$2.2M
NCATS NIH HHS UL1 TR000454NIBIB NIH HHS T32 EB006343NICHD NIH HHS DP2 HD091793
6 · The paper itself

Abstract

CRISPR-associated proteins (Cas) are enabling powerful new approaches to control mammalian cell functions, yet the lack of spatially defined, noninvasive modalities limits their use as biological tools. Here, we integrate thermal gene switches with dCas9 complexes to confer remote control of gene activation and suppression with short pulses of heat. Using a thermal switch constructed from the heat shock protein A6 (HSPA6) locus, we show that a single heat pulse 3-5 °C above basal temperature is sufficient to trigger expression of dCas9 complexes. We demonstrate that dCas9 fused to the transcriptional activator VP64 is functional after heat activation, and, depending on the number of heat pulses, drives transcription of endogenous genes

Indexed as

CRISPR-Cas SystemsAnimalsChemokine CCL21CRISPR-Associated Protein 9Genes, SwitchGranzymesGreen Fluorescent ProteinsHEK293 CellsHerpes Simplex Virus Protein Vmw65Hot TemperatureHSP70 Heat-Shock ProteinsHumansKruppel-Like Transcription FactorsMice, NudeProtein DomainsRecombinant Fusion ProteinsCCL21 protein, humanChemokine CCL21CRISPR-Associated Protein 9GranzymesGreen Fluorescent ProteinsGZMB protein, humanHerpes Simplex Virus Protein Vmw65HSP70 Heat-Shock ProteinsHSPA6 protein, humanKruppel-Like Transcription FactorsRecombinant Fusion ProteinsRepressor ProteinsZNF10 protein, human

Identifiers

PMID31904924
PMCPMC7035993
OpenAlexW2996781974

What OpenQuestion holds

Textmetadata
LicenceTDM
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.