MOLECULAR-BASIS OF MYOTONIC-DYSTROPHY - EXPANSION OF A TRINUCLEOTIDE (CTG) REPEAT AT THE 3' END OF A TRANSCRIPT ENCODING A PROTEIN-KINASE FAMILY MEMBER

被引:2193
作者
BROOK, JD
MCCURRACH, ME
HARLEY, HG
BUCKLER, AJ
CHURCH, D
ABURATANI, H
HUNTER, K
STANTON, VP
THIRION, JP
HUDSON, T
SOHN, R
ZEMELMAN, B
SNELL, RG
RUNDLE, SA
CROW, S
DAVIES, J
SHELBOURNE, P
BUXTON, J
JONES, C
JUVONEN, V
JOHNSON, K
HARPER, PS
SHAW, DJ
HOUSMAN, DE
机构
[1] UNIV WALES COLL MED, INST MED GENET, CARDIFF CF4 4XN, S GLAM, WALES
[2] CHARING CROSS & WESTMINSTER MED SCH, DEPT ANAT, LONDON W6 8RF, ENGLAND
关键词
D O I
10.1016/0092-8674(92)90154-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Using positional cloning strategies, we have identified a CTG triplet repeat that undergoes expansion in myotonic dystrophy patients. This sequence is highly variable in the normal population. PCR analysis of the interval containing this repeat indicates that unaffected individuals have between 5 and 27 copies. Myotonic dystrophy patients who are minimally affected have at least 50 repeats, while more severely affected patients have expansion of the repeat containing segment up to several kilobase pairs. The CTG repeat is transcribed and is located in the 3' untranslated region of an mRNA that is expressed in tissues affected by myotonic dystrophy. This mRNA encodes a polypeptide that is a member of the protein kinase family.
引用
收藏
页码:799 / 808
页数:10
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