Evidence map›Paper›PMID 30368256›Full record

ArticleSkeletal muscle2018

A novel tetracycline-responsive transgenic mouse strain for skeletal muscle-specific gene expression.

Masahiro Iwata, Davis A Englund, Yuan Wen, Cory M Dungan, Kevin A Murach, Ivan J Vechetti, Christopher B Mobley, Charlotte A Peterson, John J McCarthy

Open access · goldAbstract read
In one paragraph

Article in Skeletal muscle, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
1.8field-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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

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  10. The Placenta Regulates Intrauterine Fetal Growth via Exosomal PPARγ.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
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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

9 authors at 2 institutions in 2 countries.

Masahiro IwataThe Center for Muscle Biology, University of Kentucky, Lexington, KY, 40536, USA.
Davis A EnglundThe Center for Muscle Biology, University of Kentucky, Lexington, KY, 40536, USA.
Yuan WenThe Center for Muscle Biology, University of Kentucky, Lexington, KY, 40536, USA.
Cory M DunganThe Center for Muscle Biology, University of Kentucky, Lexington, KY, 40536, USA.
Kevin A MurachThe Center for Muscle Biology, University of Kentucky, Lexington, KY, 40536, USA.
Ivan J VechettiThe Center for Muscle Biology, University of Kentucky, Lexington, KY, 40536, USA.
Christopher B MobleyThe Center for Muscle Biology, University of Kentucky, Lexington, KY, 40536, USA.
Charlotte A PetersonThe Center for Muscle Biology, University of Kentucky, Lexington, KY, 40536, USA.
John J McCarthyThe Center for Muscle Biology, University of Kentucky, Lexington, KY, 40536, USA. jjmcca2@uky.edu.
University of Kentucky · USNihon Fukushi University · JP

Funding

NRSA Training CoreTL1TR001997 · NCATS · UNIVERSITY OF KENTUCKY · PI PENDERGAST, JULIE S, STOOPS, WILLIAM WALTON · 2016 to 2025
$4.2M
The role of satellite cells in adult skeletal muscle growth and maintenanceR01AR060701 · NIAMS · UNIVERSITY OF KENTUCKY · PI MCCARTHY, JOHN JOSEPH, PETERSON, CHARLOTTE A. · 2010 to 2019
$3.3M
The effects of exercise on satellite cell dynamics during agingR01AG049806 · NIA · UNIVERSITY OF KENTUCKY · PI MCCARTHY, JOHN JOSEPH, PETERSON, CHARLOTTE A. · 2016 to 2020
$1.8M
Fusion-Independent Roles of Satellite Cells in Muscle AdaptationF32AR071753 · NIAMS · UNIVERSITY OF KENTUCKY · PI MURACH, KEVIN · 2017 to 2019
$184k
Determining the fiber type-specific requirements for satellite cells during skeletal muscle hypertrophyF31AR075364 · NIAMS · UNIVERSITY OF KENTUCKY · PI ENGLUND, DAVIS A. · 2020 to 2020
$17k
NCATS NIH HHS TL1 TR001997NIAMS NIH HHS F31 AR075364NIAMS NIH HHS F32 AR071753NIAMS NIH HHS R01 AR060701NIA NIH HHS R01 AG049806NIH HHS AG049806NIH HHS AR060701NIH HHS AR071753
6 · The paper itself

Abstract

backgroundThe tetracycline-responsive system (Tet-ON/OFF) has proven to be a valuable tool for manipulating gene expression in an inducible, temporal, and tissue-specific manner. The purpose of this study was to create and characterize a new transgenic mouse strain utilizing the human skeletal muscle α-actin (HSA) promoter to drive skeletal muscle-specific expression of the reverse tetracycline transactivator (rtTA) gene which we have designated as the HSA-rtTA mouse.

methodsTo confirm the HSA-rtTA mouse was capable of driving skeletal muscle-specific expression, we crossed the HSA-rtTA mouse with the tetracycline-responsive histone H2B-green fluorescent protein (H2B-GFP) transgenic mouse in order to label myonuclei.

resultsReverse transcription-PCR confirmed skeletal muscle-specific expression of rtTA mRNA, while single-fiber analysis showed highly effective GFP labeling of myonuclei in both fast- and slow-twitch skeletal muscles. Pax7 immunohistochemistry of skeletal muscle cross-sections revealed no appreciable GFP expression in satellite cells.

conclusionsThe HSA-rtTA transgenic mouse allows for robust, specific, and inducible gene expression across muscles of different fiber types. The HSA-rtTA mouse provides a powerful tool to manipulate gene expression in skeletal muscle.

Indexed as

TransgenesAnimalsGene TargetingGreen Fluorescent ProteinsHumansMiceMice, Inbred C57BLMuscle, SkeletalPAX7 Transcription FactorTetracyclineTrans-ActivatorsGreen Fluorescent ProteinsPax7 protein, mousePAX7 Transcription FactorTetracyclineTrans-ActivatorsSkeletal muscle-specificTetracycline-responsive

Identifiers

PMID30368256
PMCPMC6204038
OpenAlexW2898387792

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.