Evidence map›Paper›PMID 30582405›Full record

ArticleCell cycle (Georgetown, Tex.)2019

Conditional gene inactivation by combining tetracycline-mediated transcriptional repression and auxin-inducible degron-mediated degradation.

Lau Yan Ng, Hoi Tang Ma, Julio C Y Liu, Xiner Huang, Nelson Lee, Randy Y C Poon

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed, 18 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

6 authors at 1 institution in 1 country.

Lau Yan Nga Division of Life Science, Center for Cancer Research, and State Key Laboratory of Molecular Neuroscience , Hong Kong University of Science and Technology , Kowloon , Hong Kong.ORCID 0000-0002-9098-8352
Hoi Tang Maa Division of Life Science, Center for Cancer Research, and State Key Laboratory of Molecular Neuroscience , Hong Kong University of Science and Technology , Kowloon , Hong Kong.
Julio C Y Liua Division of Life Science, Center for Cancer Research, and State Key Laboratory of Molecular Neuroscience , Hong Kong University of Science and Technology , Kowloon , Hong Kong.
Xiner Huanga Division of Life Science, Center for Cancer Research, and State Key Laboratory of Molecular Neuroscience , Hong Kong University of Science and Technology , Kowloon , Hong Kong.ORCID 0000-0002-0154-8372
Nelson Leea Division of Life Science, Center for Cancer Research, and State Key Laboratory of Molecular Neuroscience , Hong Kong University of Science and Technology , Kowloon , Hong Kong.
Randy Y C Poona Division of Life Science, Center for Cancer Research, and State Key Laboratory of Molecular Neuroscience , Hong Kong University of Science and Technology , Kowloon , Hong Kong.
Hong Kong University of Science and Technology · HK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Characterizing the functions of essential cell cycle control genes requires tight and rapid inducible gene inactivation. Drawbacks of current conditional depletion approaches include slow responses and incomplete depletion. We demonstrated that by integrating the tetracycline-controlled promoter system and the auxin-inducible degron (AID) system together, AID-tagged proteins can be downregulated more efficiently than the individual technology alone. When used in conjunction with CRISPR-Cas9-mediated disruption of the endogenous locus, this system facilitates the analysis of essential genes by allowing rapid and tight conditional depletion, as we have demonstrated using several cell cycle-regulatory genes including cyclin A, CDK2, and TRIP13. The vectors constructed in this study allow expression of AID-fusion proteins under the control of tetracycline-controlled promoters and should be useful in studies requiring rapid and tight suppression of gene expression in mammalian cells.

Indexed as

ProteolysisATPases Associated with Diverse Cellular ActivitiesCell Cycle ProteinsClone CellsClustered Regularly Interspaced Short Palindromic RepeatsCRISPR-Cas SystemsCyclin ACyclin-Dependent Kinase 2Gene ExpressionGene Knockout TechniquesHeLa CellsHumansIndoleacetic AcidsResponse ElementsRetroviridaeTetracyclinesATPases Associated with Diverse Cellular ActivitiesCDK2 protein, humanCell Cycle ProteinsCyclin ACyclin-Dependent Kinase 2Indoleacetic AcidsTetracyclinesTRIP13 protein, humanInducible degronknockoutmethods

Identifiers

PMID30582405
PMCPMC6343694
OpenAlexW2906573880

What OpenQuestion holds

Textmetadata
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.