Evidence map›Paper›PMID 36995025›Full record

ArticleJournal of cell science2023

A robust dual gene ON-OFF toggle directed by two independent promoter-degron pairs.

Tsz Kwan Yeung, Sehong Kim, Hoi Tang Ma, Randy Y C Poon

Open access · hybridAbstract read
In one paragraph

Article in Journal of cell science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

5 citing papers in PubMed, 4 citations in OpenAlex.

  1. GET3 regulates apoptosis via tail-anchoring of MCL1.Cell death and differentiation · 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

4 authors at 2 institutions in 2 countries.

Tsz Kwan YeungDivision of Life Science, Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong.
Sehong KimDivision of Life Science, Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong.
Hoi Tang MaDepartment of Pathology, The University of Hong Kong, Hong Kong.
Randy Y C PoonDivision of Life Science, Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong.ORCID 0000-0001-5571-6231
Hong Kong University of Science and Technology · HKChinese University of Hong Kong · HK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Switching genes on and off on cue is a cornerstone for understanding gene functions. One contemporary approach for loss-of-function studies of essential genes involves CRISPR-mediated knockout of the endogenous locus in conjunction with the expression of a rescue construct, which can subsequently be turned off to produce a gene inactivation effect in mammalian cell lines. A broadening of this approach would involve simultaneously switching on a second construct to interrogate the functions of a gene in the pathway. In this study, we developed a pair of switches that were independently controlled by both inducible promoters and degrons, enabling the toggling between two constructs with comparable kinetics and tightness. The gene-OFF switch was based on TRE transcriptional control coupled with auxin-induced degron-mediated proteolysis. A second independently controlled gene-ON switch was based on a modified ecdysone promoter and mutated FKBP12-derived destabilization domain degron, allowing acute and tuneable gene activation. This platform facilitates efficient generation of knockout cell lines containing a two-gene switch that is regulated tightly and can be flipped within a fraction of the time of a cell cycle.

Indexed as

Gene Expression RegulationIndoleacetic AcidsAnimalsCell LineMammalsPromoter Regions, GeneticProteolysisIndoleacetic AcidsAuxin-inducible degronCRISPREssential genesKnockout

Identifiers

PMID36995025
PMCPMC10198621
OpenAlexW4361271916

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.