Evidence map›Paper›PMID 28431041›Full record

ArticleNucleic acids research2017

Bidirectional approaches for optogenetic regulation of gene expression in mammalian cells using Arabidopsis cryptochrome 2.

Gopal P Pathak, Jessica I Spiltoir, Camilla Höglund, Lauren R Polstein, Sari Heine-Koskinen, Charles A Gersbach, Jari Rossi, Chandra L Tucker

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
16.2field-weighted citation impact, top 1% 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

33 citing papers in PubMed, 68 citations in OpenAlex.

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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

8 authors at 3 institutions in 2 countries.

Gopal P PathakDepartment of Pharmacology, University of Colorado School of Medicine, Aurora, CO 80045, USA.
Jessica I SpiltoirDepartment of Pharmacology, University of Colorado School of Medicine, Aurora, CO 80045, USA.
Camilla HöglundDepartment of Anatomy, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
Lauren R PolsteinDepartment of Biomedical Engineering, Duke University, Durham, NC 27708, USA.
Sari Heine-KoskinenDepartment of Anatomy, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
Charles A GersbachDepartment of Biomedical Engineering, Duke University, Durham, NC 27708, USA.
Jari RossiDepartment of Anatomy, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
Chandra L TuckerDepartment of Pharmacology, University of Colorado School of Medicine, Aurora, CO 80045, USA.
University of Colorado Denver · USUniversity of Helsinki · FIDuke University · US

Funding

ZEBRAFISH TRANSGENIC CORE - ROCKY MOUNTAIN NEUROLOGICAL DISORDERS CORE CENTERP30NS048154 · NINDS · UNIVERSITY OF COLORADO DENVER · PI RIBERA, ANGELES BADELL · 2004 to 2020
$10.1M
Control of Protein Activity Via Light Stimulated DimerizersR01GM100225 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI TUCKER, CHANDRA L · 2012 to 2019
$3.3M
Engineering Targeted Epigenetic Modifiers for Precise Control of Gene RegulationR01DA036865 · NIDA · DUKE UNIVERSITY · PI CRAWFORD, GREGORY E, GERSBACH, CHARLES A. · 2013 to 2017
$2.6M
NIDA NIH HHS R01 DA036865NIGMS NIH HHS R01 GM100225NINDS NIH HHS P30 NS048154
6 · The paper itself

Abstract

Optogenetic tools allow regulation of cellular processes with light, which can be delivered with spatiotemporal resolution. In previous work, we used cryptochrome 2 (CRY2) and CIB1, Arabidopsis proteins that interact upon light illumination, to regulate transcription with light in yeast. While adopting this approach to regulate transcription in mammalian cells, we observed light-dependent redistribution and clearing of CRY2-tethered proteins within the nucleus. The nuclear clearing phenotype was dependent on the presence of a dimerization domain contained within the CRY2-fused transcriptional activators. We used this knowledge to develop two different approaches to regulate cellular protein levels with light: a system using CRY2 and CIB1 to induce protein expression with light through stimulation of transcription, and a system using CRY2 and a LOV-fused degron to simultaneously block transcription and deplete protein levels with light. These tools will allow precise, bi-directional control of gene expression in a variety of cells and model systems.

Indexed as

Gene Expression RegulationAnimalsAnimals, Genetically ModifiedArabidopsisArabidopsis ProteinsBasic Helix-Loop-Helix ProteinsCell LineCryptochromesDNA-Binding ProteinsHEK293 CellsHumansLightOptogeneticsTranscriptional ActivationZebrafishArabidopsis ProteinsBasic Helix-Loop-Helix ProteinsCIB1 protein, ArabidopsisCRY2 protein, ArabidopsisCryptochromesDNA-Binding ProteinsLOV1 protein, Arabidopsis

Identifiers

PMID28431041
PMCPMC5714224
OpenAlexW2605740017

What OpenQuestion holds

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LicenceCC BY-NC
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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.