Cargando…

microRNA-mRNA Profile of Skeletal Muscle Differentiation and Relevance to Congenital Myotonic Dystrophy

microRNAs (miRNAs) regulate messenger RNA (mRNA) abundance and translation during key developmental processes including muscle differentiation. Assessment of miRNA targets can provide insight into muscle biology and gene expression profiles altered by disease. mRNA and miRNA libraries were generated...

Descripción completa

Detalles Bibliográficos
Autores principales: Morton, Sarah U., Sefton, Christopher R., Zhang, Huanqing, Dai, Manhong, Turner, David L., Uhler, Michael D., Agrawal, Pankaj B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7962092/
https://www.ncbi.nlm.nih.gov/pubmed/33799993
http://dx.doi.org/10.3390/ijms22052692
_version_ 1783665403186118656
author Morton, Sarah U.
Sefton, Christopher R.
Zhang, Huanqing
Dai, Manhong
Turner, David L.
Uhler, Michael D.
Agrawal, Pankaj B.
author_facet Morton, Sarah U.
Sefton, Christopher R.
Zhang, Huanqing
Dai, Manhong
Turner, David L.
Uhler, Michael D.
Agrawal, Pankaj B.
author_sort Morton, Sarah U.
collection PubMed
description microRNAs (miRNAs) regulate messenger RNA (mRNA) abundance and translation during key developmental processes including muscle differentiation. Assessment of miRNA targets can provide insight into muscle biology and gene expression profiles altered by disease. mRNA and miRNA libraries were generated from C2C12 myoblasts during differentiation, and predicted miRNA targets were identified based on presence of miRNA binding sites and reciprocal expression. Seventeen miRNAs were differentially expressed at all time intervals (comparing days 0, 2, and 5) of differentiation. mRNA targets of differentially expressed miRNAs were enriched for functions related to calcium signaling and sarcomere formation. To evaluate this relationship in a disease state, we evaluated the miRNAs differentially expressed in human congenital myotonic dystrophy (CMD) myoblasts and compared with normal control. Seventy-four miRNAs were differentially expressed during healthy human myocyte maturation, of which only 12 were also up- or downregulated in CMD patient cells. The 62 miRNAs that were only differentially expressed in healthy cells were compared with differentiating C2C12 cells. Eighteen of the 62 were conserved in mouse and up- or down-regulated during mouse myoblast differentiation, and their C2C12 targets were enriched for functions related to muscle differentiation and contraction.
format Online
Article
Text
id pubmed-7962092
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-79620922021-03-17 microRNA-mRNA Profile of Skeletal Muscle Differentiation and Relevance to Congenital Myotonic Dystrophy Morton, Sarah U. Sefton, Christopher R. Zhang, Huanqing Dai, Manhong Turner, David L. Uhler, Michael D. Agrawal, Pankaj B. Int J Mol Sci Article microRNAs (miRNAs) regulate messenger RNA (mRNA) abundance and translation during key developmental processes including muscle differentiation. Assessment of miRNA targets can provide insight into muscle biology and gene expression profiles altered by disease. mRNA and miRNA libraries were generated from C2C12 myoblasts during differentiation, and predicted miRNA targets were identified based on presence of miRNA binding sites and reciprocal expression. Seventeen miRNAs were differentially expressed at all time intervals (comparing days 0, 2, and 5) of differentiation. mRNA targets of differentially expressed miRNAs were enriched for functions related to calcium signaling and sarcomere formation. To evaluate this relationship in a disease state, we evaluated the miRNAs differentially expressed in human congenital myotonic dystrophy (CMD) myoblasts and compared with normal control. Seventy-four miRNAs were differentially expressed during healthy human myocyte maturation, of which only 12 were also up- or downregulated in CMD patient cells. The 62 miRNAs that were only differentially expressed in healthy cells were compared with differentiating C2C12 cells. Eighteen of the 62 were conserved in mouse and up- or down-regulated during mouse myoblast differentiation, and their C2C12 targets were enriched for functions related to muscle differentiation and contraction. MDPI 2021-03-07 /pmc/articles/PMC7962092/ /pubmed/33799993 http://dx.doi.org/10.3390/ijms22052692 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Morton, Sarah U.
Sefton, Christopher R.
Zhang, Huanqing
Dai, Manhong
Turner, David L.
Uhler, Michael D.
Agrawal, Pankaj B.
microRNA-mRNA Profile of Skeletal Muscle Differentiation and Relevance to Congenital Myotonic Dystrophy
title microRNA-mRNA Profile of Skeletal Muscle Differentiation and Relevance to Congenital Myotonic Dystrophy
title_full microRNA-mRNA Profile of Skeletal Muscle Differentiation and Relevance to Congenital Myotonic Dystrophy
title_fullStr microRNA-mRNA Profile of Skeletal Muscle Differentiation and Relevance to Congenital Myotonic Dystrophy
title_full_unstemmed microRNA-mRNA Profile of Skeletal Muscle Differentiation and Relevance to Congenital Myotonic Dystrophy
title_short microRNA-mRNA Profile of Skeletal Muscle Differentiation and Relevance to Congenital Myotonic Dystrophy
title_sort microrna-mrna profile of skeletal muscle differentiation and relevance to congenital myotonic dystrophy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7962092/
https://www.ncbi.nlm.nih.gov/pubmed/33799993
http://dx.doi.org/10.3390/ijms22052692
work_keys_str_mv AT mortonsarahu micrornamrnaprofileofskeletalmuscledifferentiationandrelevancetocongenitalmyotonicdystrophy
AT seftonchristopherr micrornamrnaprofileofskeletalmuscledifferentiationandrelevancetocongenitalmyotonicdystrophy
AT zhanghuanqing micrornamrnaprofileofskeletalmuscledifferentiationandrelevancetocongenitalmyotonicdystrophy
AT daimanhong micrornamrnaprofileofskeletalmuscledifferentiationandrelevancetocongenitalmyotonicdystrophy
AT turnerdavidl micrornamrnaprofileofskeletalmuscledifferentiationandrelevancetocongenitalmyotonicdystrophy
AT uhlermichaeld micrornamrnaprofileofskeletalmuscledifferentiationandrelevancetocongenitalmyotonicdystrophy
AT agrawalpankajb micrornamrnaprofileofskeletalmuscledifferentiationandrelevancetocongenitalmyotonicdystrophy