Your browser doesn't support javascript.
loading
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.
Afiliación
  • Morton SU; Division of Newborn Medicine, Boston Children's Hospital, Boston, MA 02115, USA.
  • Sefton CR; Department of Pediatrics, Harvard Medical School, Boston, MA 02115, USA.
  • Zhang H; School of Medicine, University of North Carolina, Chapel Hill, NC 27516, USA.
  • Dai M; Michigan Neuroscience Institute, University of Michigan, Ann Arbor, MI 48109, USA.
  • Turner DL; Michigan Neuroscience Institute, University of Michigan, Ann Arbor, MI 48109, USA.
  • Uhler MD; Michigan Neuroscience Institute, University of Michigan, Ann Arbor, MI 48109, USA.
  • Agrawal PB; Department of Biological Chemistry, University of Michigan, Ann Arbor, MI 48109, USA.
Int J Mol Sci ; 22(5)2021 Mar 07.
Article en En | MEDLINE | ID: mdl-33799993
ABSTRACT
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.
Asunto(s)
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: ARN Mensajero / Músculo Esquelético / Mioblastos / MicroARNs / Distrofia Miotónica Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Int J Mol Sci Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: ARN Mensajero / Músculo Esquelético / Mioblastos / MicroARNs / Distrofia Miotónica Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Int J Mol Sci Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos