BETA-SARCOGLYCAN - CHARACTERIZATION AND ROLE IN LIMB-GIRDLE MUSCULAR-DYSTROPHY LINKED TO 4Q12

被引:431
作者
LIM, LE
DUCLOS, F
BROUX, O
BOURG, N
SUNADA, Y
ALLAMAND, V
MEYER, J
RICHARD, IZ
MOOMAW, C
SLAUGHTER, C
TOME, FMS
FARDEAU, M
JACKSON, CE
BECKMANN, JS
CAMPBELL, KP
机构
[1] UNIV IOWA,COLL MED,HOWARD HUGHES MED INST,IOWA CITY,IA 52242
[2] UNIV IOWA,COLL MED,DEPT PHYSIOL & BIOPHYS,IOWA CITY,IA 52242
[3] CTR ETUD POLYMORPHISME HUMAIN,FDN JEAN DAUSSET,F-75010 PARIS,FRANCE
[4] GENETHON SA,F-91000 EVRY,FRANCE
[5] UNIV TEXAS,HOWARD HUGHES MED INST,BIOPOLYMER FACIL,DALLAS,TX 75235
[6] INSERM,U153,F-75005 PARIS,FRANCE
[7] HENRY FORD HOSP,DIV CLIN & MOLEC GENET,DETROIT,MI 48202
关键词
D O I
10.1038/ng1195-257
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
beta-sarcoglycan, a 43 kDa dystrophin-associated glycoprotein, is an integral component of the dystrophin-glycoprotein complex. We have cloned human beta-sarcoglycan cDNA and mapped the beta-sarcoglycan gene to chromosome 4q12. Pericentromeric markers and an intragenic polymorphic CA repeat cosegregated perfectly with autosomal recessive limb-girdle muscular dystrophy in several Amish families. A Thr-to-Arg missense mutation was identified within the beta-sarcoglycan gene that leads to a dramatically reduced expression of beta-sarcoglycan in the sarcolemma and a concomitant loss of adhalin and 35 DAG, which may represent a disruption of a functional subcomplex within the dystrophin-glycoprotein complex. Thus, the beta-sarcoglycan gene is the fifth locus identified (LGMD2E) that is involved in autosomal recessive limb-girdle muscular dystrophy.
引用
收藏
页码:257 / 265
页数:9
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