|Reecy, James - IOWA STATE UNIV., AMES|
|Potts, Jacyln - IOWA STATE UNIV., AMES|
Submitted to: Plant and Animal Genome VX Conference Abstracts
Publication Type: Proceedings
Publication Acceptance Date: November 1, 2001
Publication Date: November 1, 2001
Technical Abstract: Mutations in myostatin result in the double muscling phenotype in cattle. However, the molecular mechanisms whereby inactivation of myostatin results in increased skeletal muscle mass have not yet been identified. Furthermore, quantitative trait loci (QTL) have been recently identified that interact with myostatin. Thus, there is a need to identify genes that lie downstream of myostatin. To begin to address these questions, we chose to identify genes that were differentially expressed in 31 - 33 day wild type and double-muscle bovine embryos. We believe that genes that are differentially expressed in wild-type and double-muscle cattle will 1) make good candidates for genes that interact with myostatin and 2) provide insights into the molecular mechanisms whereby myostatin represses skeletal muscle growth. By suppressive subtractive hybridization, we identified numerous genes whose expression differed between double-muscled and wild type bovine embryos. Many of these genes appear to be involved in cell proliferation, transcription and protein synthesis, all of which are biological systems know to be influenced by myostatin. Furthermore, COMPASS analysis suggests that several of these genes reside within the previously identified QTL that interact with myostatin. A number of strategies are now being pursued to identify additional candidate genes and to test whether previously identified genes interact with myostatin.