| First Author | Lumeng CN | Year | 1999 |
| Journal | Hum Mol Genet | Volume | 8 |
| Issue | 4 | Pages | 593-9 |
| PubMed ID | 10072426 | Mgi Jnum | J:54556 |
| Mgi Id | MGI:1336485 | Doi | 10.1093/hmg/8.4.593 |
| Citation | Lumeng CN, et al. (1999) Characterization of dystrophin and utrophin diversity in the mouse. Hum Mol Genet 8(4):593-9 |
| abstractText | Utrophin is a 400 kDa autosomal homolog of dystrophin and a component of the submembranous cytoskeleton. While multiple dystrophin isoforms have been identified along with alternatively spliced products, to date only two different mRNA species of utrophin have been identified. To determine the degree of evolutionary conservation between dystrophin and utrophin isoforms, we have compared their expression patterns in adult mice. Northern blot analysis of multiple adult tissues confirmed that only two major sizes of transcripts are produced from each gene: 13 and 5.5 kb from utrophin and 14 and 4.8 kb from dystrophin. However, western blot analysis detected several putative short utrophin isoforms that may be homologs of the dystrophin isoforms Dp140, Dp116 and Dp71. We also identified an alternatively spliced utrophin transcript that lacks the equivalent of the alternatively spliced dystrophin exon 71. Finally, we demonstrated that the C-terminal domain of utrophin targeted to neuromuscular junctions in normal mice, but localized to the sarcolemma efficiently only in the absence of dystrophin. Our results provide further evidence for a common evolutionary origin of the utrophin and dystrophin genes. |
