Myotonic Dystrophy Type 2 Caused by a CCTG Expansion in Intron 1 of ZNF9
2001; American Association for the Advancement of Science; Volume: 293; Issue: 5531 Linguagem: Inglês
10.1126/science.1062125
ISSN1095-9203
AutoresChristina L. Liquori, K. Ricker, Melinda L. Moseley, Jennifer F. Jacobsen, Wolfram Kreß, Susan L. Naylor, John Day, Laura P.W. Ranum,
Tópico(s)Cardiomyopathy and Myosin Studies
ResumoMyotonic dystrophy (DM), the most common form of muscular dystrophy in adults, can be caused by a mutation on either chromosome 19q13 (DM1) or 3q21 (DM2/PROMM). DM1 is caused by a CTG expansion in the 3′ untranslated region of the dystrophia myotonica–protein kinase gene ( DMPK ). Several mechanisms have been invoked to explain how this mutation, which does not alter the protein-coding portion of a gene, causes the specific constellation of clinical features characteristic of DM. We now report that DM2 is caused by a CCTG expansion (mean ∼5000 repeats) located in intron 1 of the zinc finger protein 9 ( ZNF9 ) gene. Parallels between these mutations indicate that microsatellite expansions in RNA can be pathogenic and cause the multisystemic features of DM1 and DM2.
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