Target genes of myostatin loss-of-function in muscles of late bovine fetuses

• Main Authors: Hocquette Jean-François, Léger Jean, Bernard Carine, Passelaigue Florent, Cassar-Malek Isabelle
• Format: Article
• Language: English
• Published: BMC 2007-03-01
• Series: BMC Genomics
• Online Access: http://www.biomedcentral.com/1471-2164/8/63

<p>Abstract</p> <p>Background</p> <p>Myostatin, a muscle-specific member of the Transforming Growth Factor beta family, negatively regulates muscle development. Double-muscled (DM) cattle have a loss-of-function mutation in their myostatin gene responsible for the hypermuscular phenotype. Thus, these animals are a good model for understanding the mechanisms underpinning muscular hypertrophy. In order to identify individual genes or networks that may be myostatin targets, we looked for genes that were differentially expressed between DM and normal (NM) animals (n = 3 per group) in the <it>semitendinosus </it>muscle (hypertrophied in DM animals) at 260 days of fetal development (when the biochemical differentiation of muscle is intensive). A heterologous microarray (human and murine oligonucleotide sequences) of around 6,000 genes expressed in muscle was used.</p> <p>Results</p> <p>Many genes were found to be differentially expressed according to genetic type (some with a more than 5-fold change), and according to the presence of one or two functional myostatin allele(s). They belonged to various functional categories. The genes down-regulated in DM fetuses were mainly those encoding extracellular matrix proteins, slow contractile proteins and ribosomal proteins. The genes up-regulated in DM fetuses were mainly involved in the regulation of transcription, cell cycle/apoptosis, translation or DNA metabolism. These data highlight features indicating that DM muscle is shifted towards a more glycolytic metabolism, and has an altered extracellular matrix composition (e.g. down-regulation of <it>COL1A1 </it>and <it>COL1A2</it>, and up-regulation of <it>COL4A2</it>) and decreased adipocyte differentiation (down-regulation of <it>C1QTNF3</it>). The altered gene expression in the three major muscle compartments (fibers, connective tissue and intramuscular adipose tissue) is consistent with the well-known characteristics of DM cattle. In addition, novel potential targets of the myostatin gene were identified (MB, PLN, troponins, <it>ZFHX1B</it>).</p> <p>Conclusion</p> <p>Thus, the myostatin loss-of-function mutation affected several physiological processes involved in the development and determination of the functional characteristics of muscle tissue.</p>