| Literature DB >> 16099459 |
Fumiaki Yokoi1, Mai T Dang, Shinichi Mitsui, Yuqing Li.
Abstract
Mutations of SGCE encoding epsilon-sarcoglycan cause myoclonus-dystonia. SGCE is paternally expressed; however, 5-10% of patients show maternal inheritance of the disease. We found Sgce was exclusively paternally expressed in mice by using a novel polymorphism marker. The result was confirmed in Sgce heterozygous knockout mice. This finding suggests that maternally inherited myoclonus-dystonia may not result from maternal expression of SGCE. Furthermore, we report a new family of alternatively spliced Sgce mRNA expressed in the brain coding for different C-terminal sequences possessing a PDZ-binding motif. Our results provide a better basis for diagnosis and understanding of the pathogenesis of myoclonus-dystonia.Entities:
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Year: 2005 PMID: 16099459 DOI: 10.1016/j.febslet.2005.07.065
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124