IDENTIFICATION OF MUTATIONS IN THE PUTATIVE ATP-BINDING DOMAIN OF THE ADRENOLEUKODYSTROPHY GENE

被引:73
|
作者
FANEN, P
GUIDOUX, S
SARDE, CO
MANDEL, JL
GOOSSENS, M
AUBOURG, P
机构
[1] HOP HENRI MONDOR,INSERM,U91,MOLEC GENET LAB,F-94010 CRETEIL,FRANCE
[2] HOP ST VINCENT DE PAUL,INSERM,U342,F-75014 PARIS,FRANCE
[3] FAC MED STRASBOURG,INSERM,U184,CNRS,GENET MOLEC EUCARYOTES LAB,F-67085 STRASBOURG,FRANCE
[4] CHRU,F-67085 STRASBOURG,FRANCE
来源
JOURNAL OF CLINICAL INVESTIGATION | 1994年 / 94卷 / 02期
关键词
PEROXISOMAL DISORDER; POINT MUTATIONS; ABC TRANSPORTER; DENATURING GRADIENT GEL ELECTROPHORESIS; X-LINKED GENETIC DISEASE;
D O I
10.1172/JCI117363
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The recently identified adrenoleukodystrophy (ALD) gene is predicted to encode a peroxisomal protein of 745 amino acids that includes one domain for ATP-binding, termed nucleotide-binding fold (NBF). To determine whether mutations occur in the putative NBF of ALD protein, we analyzed by denaturing gradient gel electrophoresis (DGGE) exon 6 and 8 that encode most part of this domain in 50 ALD patients. Four amino acid substitutions, three frameshift mutations leading to premature termination signal, and a splicing mutation mere identified. These amino acid substitutions occurred at residues highly conserved in other ATP-binding cassette (ABC) proteins. In addition, a nonsense mutation was detected in exon 4.
引用
收藏
页码:516 / 520
页数:5
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