SEQUENCES OF JUNCTION FRAGMENTS IN THE DELETION-PRONE REGION OF THE DYSTROPHIN GENE

被引:47
作者
LOVE, DR
ENGLAND, SB
SPEER, A
MARSDEN, RF
BLOOMFIELD, JF
ROCHE, AL
CROSS, GS
MOUNTFORD, RC
SMITH, TJ
DAVIES, KE
机构
[1] ACAD SCI GDR,INST MOLEC BIOL,DEPT CELL DIFFERENTIAT,O-1115 BERLIN,GERMANY
[2] ST MARYS HOSP,DEPT GENET,MANCHESTER M13 0JH,LANCS,ENGLAND
[3] CITY HOSP NOTTINGHAM,MOLEC GENET UNIT,NOTTINGHAM NG5 1PD,ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1016/0888-7543(91)90484-V
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The Duchenne muscular dystrophy locus is remarkable in that it shows a high mutation rate and the majority of mutations found are deletions. These deletions are generated as meiotic as well as mitotic events and occur preferentially in the central region of the gene. Nothing is known so far about the mechanisms involved. This paper reports the first sequencing of deletion junctions in the dystrophin gene. The data from a study of two patients with deletions in the central region of dystrophin show the breakpoints to lie in regions of introns in which stretches of dA-dT are seen. The relationship between these observations and possible mechanisms for the mutations is discussed. © 1991.
引用
收藏
页码:57 / 67
页数:11
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