Evidence map›Paper›PMID 31914652›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2020

CRISPR-Cas9-induced IGF1 gene activation as a tool for enhancing muscle differentiation via multiple isoform expression.

Matthew J Roberston, Suchi Raghunathan, Vladimir N Potaman, Fan Zhang, M David Stewart, Bradley K McConnell, Robert J Schwartz

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

16 citing papers in PubMed, 16 citations in OpenAlex.

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  12. The Effects of Muscle Cell Aging on Myogenesis.International journal of molecular sciences · 2021
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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

7 authors at 2 institutions in 1 country.

Matthew J RoberstonDan L. Duncan Cancer Center, Advanced Technology Core, Alkek Center for Molecular Discovery, Baylor College of Medicine, Houston, TX, USA.
Suchi RaghunathanDepartment of Pharmacological and Pharmaceutical Sciences, College of Pharmacy, University of Houston, Houston, TX, USA.
Vladimir N PotamanStem Cell Laboratory, Texas Heart Institute, Houston, TX, USA.
Fan ZhangDepartment of Pharmacological and Pharmaceutical Sciences, College of Pharmacy, University of Houston, Houston, TX, USA.
M David StewartDepartment of Biology and Biochemistry, College of Natural Sciences and Mathematics, University of Houston, Houston, TX, USA.
Bradley K McConnellDepartment of Pharmacological and Pharmaceutical Sciences, College of Pharmacy, University of Houston, Houston, TX, USA.
Robert J SchwartzStem Cell Laboratory, Texas Heart Institute, Houston, TX, USA.
University of Houston · USTargazyme (United States) · US

Funding

Gravin Signalosome Protein Coordinates Cardiac Function via Adrenergic Receptor SignalingR15HL141963 · NHLBI · UNIVERSITY OF HOUSTON · PI MCCONNELL, BRADLEY K · 2019 to 2019
$459k
Scaffolding Protein Interaction Network Regulates Cardiac Cell SignalingR15HL124458 · NHLBI · UNIVERSITY OF HOUSTON · PI MCCONNELL, BRADLEY K · 2015 to 2015
$452k
NHLBI NIH HHS R15 HL124458NHLBI NIH HHS R15 HL141963
6 · The paper itself

Abstract

Muscle wasting, or muscle atrophy, can occur with age, injury, and disease; it affects the quality of life and complicates treatment. Insulin-like growth factor 1 (IGF1) is a key positive regulator of muscle mass. The IGF1/Igf1 gene encodes multiple protein isoforms that differ in tissue expression, potency, and function, particularly in cellular proliferation and differentiation, as well as in systemic versus localized signaling. Genome engineering is a novel strategy for increasing gene expression and has the potential to recapitulate the diverse biology seen in IGF1 signaling through the overexpression of multiple IGF1 isoforms. Using a CRISPR-Cas9 gene activation approach, we showed that the expression of multiple IGF1 or Igf1 mRNA variants can be increased in human and mouse skeletal muscle myoblast cell lines using a single-guide RNA (sgRNA). We found increased IGF1 protein levels in the cell culture media and increased cellular phosphorylation of AKT1, the main effector of IGF1 signaling. We also showed that the expression of Class 1 or Class 2 mRNA variants can be selectively increased by changing the sgRNA target location. The expression of multiple IGF1 or Igf1 mRNA transcript variants in human and mouse skeletal muscle myoblasts promoted myotube differentiation and prevented dexamethasone-induced atrophy in myotubes in vitro. Our findings suggest that this novel approach for enhancing IGF1 signaling has potential therapeutic applications for treating skeletal muscle atrophy.

Indexed as

Cell DifferentiationCRISPR-Cas SystemsTranscriptional ActivationAnimalsAnti-Inflammatory AgentsBase SequenceCell ProliferationCells, CulturedDexamethasoneHumansInsulin-Like Growth Factor IMiceMuscle, SkeletalMuscular AtrophyMyoblastsPhosphorylationAnti-Inflammatory AgentsDexamethasoneInsulin-Like Growth Factor IProtein IsoformsRNA, Messengergene regulationinsulin‐like growth factor 1muscle atrophy

Identifiers

PMID31914652
PMCPMC6956731
OpenAlexW2991508455

What OpenQuestion holds

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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.