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| | BioBeat Online Magazine |
 | | Fukuyama-type congenital muscular dystrophy (FCMD), an unusual form of muscular dystrophy that is particularly common in Japan, appears to be caused by the presence of an ancient retrotransposon insertion in a newly identified gene called the FCMD gene, according to a recent report in Nature (Kobayashi, K., et al., Nature 394: 388—392, July 23, 1998). |
 | | The authors suggest that the retrotransposon insertion, or other mutations in the FCMD gene, are likely to cause a decrease in the gene’s transcription, and/or an instability in its mRNA, resulting in a loss of function. |
 | | They note that the retrotransposon insertion, which is approximately 3,000 bases long, is located in the 3’-untranslated region of the FCMD gene, and could theoretically result in an altered secondary structure for the FCMD mRNA, possibly rendering it unstable. |
| www.appliedbiosystems.com /biobeat/index.jsp?articleId=08a7de0a-97b3-27ac-fd70911fd454a521&type=0 (613 words) |
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