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SMAD7, an antagonist of TGF-beta signaling, is a candidate of prenatal skeletal muscle development and weaning weight in pigs.
- Source :
-
Molecular biology reports [Mol Biol Rep] 2016 Apr; Vol. 43 (4), pp. 241-51. Date of Electronic Publication: 2016 Feb 22. - Publication Year :
- 2016
-
Abstract
- SMAD7 promotes and enhances skeletal muscle differentiation by inhibiting transforming growth factor beta (TGF-β)/activin signaling and bone morphogenetic protein (BMP) pathways. However, its function, the mechanism regulating its translation, and its association with production meat traits remain unclear in pigs. In this study, we explored SMAD7 gene spatio-temporal and tissue distribution, conducted a single nucleotide polymorphism association analysis, and examined regulation of its expression during skeletal muscle development. We found that SMAD7 was positively related to TGF-β pathway genes and mainly expressed in prenatal developing muscle, and dual luciferase and western blot assays demonstrated that SMAD7 expression was regulated by miRNA-21 at the protein level via inhibition of mRNA translation. Finally, the association analysis showed that a single nucleotide mutation (Exon 4_28816;C/A) was significantly associated with the weaning weight of piglets among Yorkshire pigs. These data indicate that SMAD7 plays a potentially important role in mammalian prenatal skeletal muscle development and is a candidate gene for promoting greater weaning weight in pig breeding.
- Subjects :
- Amino Acid Sequence
Animals
Gene Expression Regulation, Developmental
Molecular Sequence Data
Muscle Development
Muscle, Skeletal metabolism
Organ Specificity
Phylogeny
Polymorphism, Single Nucleotide
Sequence Alignment
Smad7 Protein genetics
Smad7 Protein pharmacology
Sus scrofa metabolism
Weaning
Body Weight physiology
Muscle, Skeletal embryology
Signal Transduction
Smad7 Protein metabolism
Sus scrofa embryology
Transforming Growth Factor beta antagonists & inhibitors
Subjects
Details
- Language :
- English
- ISSN :
- 1573-4978
- Volume :
- 43
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Molecular biology reports
- Publication Type :
- Academic Journal
- Accession number :
- 26902861
- Full Text :
- https://doi.org/10.1007/s11033-016-3960-8