Evidence map›Paper›PMID 21518849›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2011

A versatile single-plasmid system for tissue-specific and inducible control of gene expression in transgenic mice.

Jae-Kyun Ko, Kyoung-Han Choi, Xiaoli Zhao, Shinji Komazaki, Zui Pan, Noah Weisleder, Jianjie Ma

Abstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
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  9. Selective inhibitory effects of zinc on cell proliferation in esophageal squamous cell carcinoma through Orai1.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2018
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  13. TRIM72 is required for effective repair of alveolar epithelial cell wounding.American journal of physiology. Lung cellular and molecular physiology · 2014
    Article
  14. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 2 countries.

Jae-Kyun KoDepartment of Physiology and Biophysics, Robert Wood Johnson Medical School, Piscataway, NJ 08854, USA.
Kyoung-Han Choi
Xiaoli Zhao
Shinji Komazaki
Zui Pan
Noah Weisleder
Jianjie Ma
Johnson University · USSaitama Medical University · JP

Funding

Modulation of MG53 Function in Cardiac Membrane RepairR01HL069000 · NHLBI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI MA, JIANJIE · 2002 to 2016
$5.3M
Ca Sparks in Muscle Aging and DystrophyR01AG028614 · NIA · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI MA, JIANJIE · 2006 to 2016
$4.1M
Calcium Regulation in the Progression of Muscular DystrophyR00AR054793 · NIAMS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI WEISLEDER, NOAH · 2011 to 2013
$730k
Calcium Regulation in the Progression of Muscular DystrophyK99AR054793 · NIAMS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI WEISLEDER, NOAH · 2008 to 2009
$159k
NHLBI NIH HHS R01 HL069000NHLBI NIH HHS R01-HL069000NIAMS NIH HHS K99 AR054793NIAMS NIH HHS K99/R00-AR054793NIAMS NIH HHS R00 AR054793NIA NIH HHS R01 AG028614NIA NIH HHS R01-AG028614
6 · The paper itself

Abstract

We describe a novel transgenic system for tissue-specific and inducible control of gene expression in mice. The system employs a tetracycline-responsive CMV promoter that controls transcription of a short-hairpin RNA (shRNA) that remains nonfunctional until an interrupting reporter cassette is excised by Cre recombinase. Insertion of Dicer and Drosha RNase processing sites within the shRNA allows generation of siRNA to knock down a target gene efficiently. Tissue-specific shRNA expression is achieved through the use of appropriate inducer mice with tissue-specific expression of Cre. We applied this system to regulate expression of junctophilins (JPs), genes essential for maintenance of membrane ultrastructure and Ca(2+) signaling in muscle. Transgenic mice with skeletal muscle-specific expression of shRNA against JP mRNAs displayed no basal change of JP expression before treatment with doxycycline (Dox), while inducible and reversible knockdown of JPs was achieved by feeding mice with Dox-containing water. Dox-induced knockdown of JPs led to abnormal junctional membrane structure and Ca(2+) signaling in adult muscle fibers, consistent with essential roles of JPs in muscle development and function. This transgenic approach can be applied for inducible and reversible gene knockdown or gene overexpression in many different tissues, thus providing a versatile system for elucidating the physiological gene function in viable animal models.

Indexed as

Genetic TechniquesAnimalsBase SequenceCHO CellsCricetinaeCricetulusGene ExpressionGene Knockdown TechniquesGenes, ReporterHEK293 CellsHumansMembrane ProteinsMiceMice, Inbred C57BLMice, TransgenicMicroscopy, Electron, TransmissionjunctophilinMembrane ProteinsRNA, Small Interfering

Identifiers

PMID21518849
PMCPMC3136336
OpenAlexW2153621609

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.