GENOMIC ORGANIZATION OF THE HUMAN DYSTROPHIN GENE ACROSS THE MAJOR DELETION HOT-SPOT AND THE 3'-REGION

被引:24
作者
NOBILE, C
GALVAGNI, F
MARCHI, J
ROBERTS, R
VITIELLO, L
机构
[1] PADUA SCH MED,DEPT BIOL,PADUA,ITALY
[2] IST NAZL RIC CANC,POPULAT GENET LAB,ALGHERO,ITALY
[3] GUYS HOSP,UNITED MED & DENT SCH,DIV MED & MOLEC GENET,PAEDIAT RES UNIT,LONDON,ENGLAND
关键词
D O I
10.1006/geno.1995.1111
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 genomic organization of most of the human dystrophin gene has not been defined at single-exon level, owing to its enormous size (2300 kb). By taking advantage of a YAC-based restriction map of the gene previously constructed, we have localized individual dystrophin exons from 42 to 79 along the central and 3' regions of the gene. These data elucidate the general organization of this large portion of the gene (1250 kb) and, in particular, characterize the genomic region most frequently involved in deletion mutations responsible for Duchenne and Becker muscular dystrophies. (C) 1995 Academic Press, Inc.
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页码:97 / 100
页数:4
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