UNSTABLE DNA-SEQUENCE IN MYOTONIC-DYSTROPHY

被引:173
作者
HARLEY, HG [1 ]
RUNDLE, SA [1 ]
REARDON, W [1 ]
MYRING, J [1 ]
CROW, S [1 ]
BROOK, JD [1 ]
HARPER, PS [1 ]
SHAW, DJ [1 ]
机构
[1] MIT,CTR CANC RES,CAMBRIDGE,MA 02139
基金
英国惠康基金;
关键词
D O I
10.1016/0140-6736(92)90729-M
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A variable DNA sequence has been detected in patients with myotonic dystrophy. We set out to determine whether identification of this specific molecular defect would improve clinical management of patients and families with myotonic dystrophy. 127 affected patients who were studied had an expanded DNA fragment not seen in 73 normal controls. The increase in length of the fragment correlated broadly with disease severity, and we noted expansion of the sequence in successive generations of the same family. Progressive expansion of the affected gene provides a molecular explanation for an apparently earlier onset in successive generations (anticipation) in myotonic dystrophy and supports the role of an unstable repeat sequence as the basis of the defect. The specificity of this finding will assist in accurate diagnosis of myotonic dystrophy and genetic counselling of affected families.
引用
收藏
页码:1125 / 1128
页数:4
相关论文
共 13 条
  • [1] CLONING OF THE ESSENTIAL MYOTONIC-DYSTROPHY REGION AND MAPPING OF THE PUTATIVE DEFECT
    ASLANIDIS, C
    JANSEN, G
    AMEMIYA, C
    SHUTLER, G
    MAHADEVAN, M
    TSILFIDIS, C
    CHEN, C
    ALLEMAN, J
    WORMSKAMP, NGM
    VOOIJS, M
    BUXTON, J
    JOHNSON, K
    SMEETS, HJM
    LENNON, GG
    CARRANO, AV
    KORNELUK, RG
    WIERINGA, B
    DEJONG, PJ
    [J]. NATURE, 1992, 355 (6360) : 548 - 551
  • [2] MOLECULAR-BASIS OF MYOTONIC-DYSTROPHY - EXPANSION OF A TRINUCLEOTIDE (CTG) REPEAT AT THE 3' END OF A TRANSCRIPT ENCODING A PROTEIN-KINASE FAMILY MEMBER
    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
    [J]. CELL, 1992, 68 (04) : 799 - 808
  • [3] DETECTION OF AN UNSTABLE FRAGMENT OF DNA SPECIFIC TO INDIVIDUALS WITH MYOTONIC-DYSTROPHY
    BUXTON, J
    SHELBOURNE, P
    DAVIES, J
    JONES, C
    VANTONGEREN, T
    ASLANIDIS, C
    DEJONG, P
    JANSEN, G
    ANVRET, M
    RILEY, B
    WILLIAMSON, R
    JOHNSON, K
    [J]. NATURE, 1992, 355 (6360) : 547 - 548
  • [4] Fleiseher B., 1918, ALBRECHT GRAEFES ARC, V96, P91, DOI DOI 10.1007/BF02018704
  • [5] AN UNSTABLE TRIPLET REPEAT IN A GENE RELATED TO MYOTONIC MUSCULAR-DYSTROPHY
    FU, YH
    PIZZUTI, A
    FENWICK, RG
    KING, J
    RAJNARAYAN, S
    DUNNE, PW
    DUBEL, J
    NASSER, GA
    ASHIZAWA, T
    DEJONG, P
    WIERINGA, B
    KORNELUK, R
    PERRYMAN, MB
    EPSTEIN, HF
    CASKEY, CT
    [J]. SCIENCE, 1992, 255 (5049) : 1256 - 1258
  • [6] HARLEY HG, 1991, AM J HUM GENET, V49, P68
  • [7] EXPANSION OF AN UNSTABLE DNA REGION AND PHENOTYPIC VARIATION IN MYOTONIC-DYSTROPHY
    HARLEY, HG
    BROOK, JD
    RUNDLE, SA
    CROW, S
    REARDON, W
    BUCKLER, AJ
    HARPER, PS
    HOUSMAN, DE
    SHAW, DJ
    [J]. NATURE, 1992, 355 (6360) : 545 - 546
  • [8] Harper P. S., 1989, MYOTONIC DYSTROPHY
  • [9] HARPER PS, 1972, LANCET, V2, P53
  • [10] HARPER PS, IN PRESS AM J HUM GE