Gene Expression Profiling of Skeletal Muscles.


Journal

Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097

Informations de publication

Date de publication:
28 10 2021
Historique:
received: 23 09 2021
revised: 21 10 2021
accepted: 27 10 2021
entrez: 27 11 2021
pubmed: 28 11 2021
medline: 17 2 2022
Statut: epublish

Résumé

Next-generation sequencing provides an opportunity for an in-depth biocomputational analysis to identify gene expression patterns between soleus and tibialis anterior, two well-characterized skeletal muscles, and analyze their gene expression profiling. RNA read counts were analyzed for differential gene expression using the R package edgeR. Differentially expressed genes were filtered using a false discovery rate of less than 0.05 c, a fold-change value of more than twenty, and an association with overrepresented pathways based on the Reactome pathway over-representation analysis tool. Most of the differentially expressed genes associated with soleus are coded for components of lipid metabolism and unique contractile elements. Differentially expressed genes associated with tibialis anterior encoded mostly for glucose and glycogen metabolic pathway regulatory enzymes and calcium-sensitive contractile components. These gene expression distinctions partly explain the genetic basis for skeletal muscle specialization, and they may help to explain skeletal muscle susceptibility to disease and drugs and further refine tissue engineering approaches.

Identifiants

pubmed: 34828324
pii: genes12111718
doi: 10.3390/genes12111718
pmc: PMC8621074
pii:
doi:

Substances chimiques

Glycogen 9005-79-2
Glucose IY9XDZ35W2

Types de publication

Comparative Study Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIAMS NIH HHS
ID : R01 AR054406
Pays : United States

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Auteurs

Sarah I Alto (SI)

Department of Pharmaceutical Sciences, College of Pharmacy, Oregon State University, Corvallis, OR 97331, USA.
Molecular and Cellular Biology Graduate Program, Graduate School, Oregon State University, Corvallis, OR 97331, USA.

Chih-Ning Chang (CN)

Department of Pharmaceutical Sciences, College of Pharmacy, Oregon State University, Corvallis, OR 97331, USA.
Molecular and Cellular Biology Graduate Program, Graduate School, Oregon State University, Corvallis, OR 97331, USA.

Kevin Brown (K)

Department of Pharmaceutical Sciences, College of Pharmacy, Oregon State University, Corvallis, OR 97331, USA.
School of Chemical, Biological, and Environmental Engineering, College of Engineering, Oregon State University, Corvallis, OR 97331, USA.

Chrissa Kioussi (C)

Department of Pharmaceutical Sciences, College of Pharmacy, Oregon State University, Corvallis, OR 97331, USA.
Molecular and Cellular Biology Graduate Program, Graduate School, Oregon State University, Corvallis, OR 97331, USA.

Theresa M Filtz (TM)

Department of Pharmaceutical Sciences, College of Pharmacy, Oregon State University, Corvallis, OR 97331, USA.
Molecular and Cellular Biology Graduate Program, Graduate School, Oregon State University, Corvallis, OR 97331, USA.

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