Identification of new mutations in the adenylosuccinate lyase gene associated with impaired enzyme activity in lymphocytes and red blood cells

被引:19
作者
Verginelli, D
Luckow, B
Crifò, C
Salerno, C
Gross, M
机构
[1] Univ Rome La Sapienza, Clin Biochem Lab, I-00185 Rome, Italy
[2] Univ Rome La Sapienza, Dept Biochem Sci, I-00185 Rome, Italy
[3] Univ Munich, Med Poliklin, D-8000 Munich, Germany
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 1998年 / 1406卷 / 01期
关键词
adenylosuccinate lyase; psychomotor retardation; purine metabolism;
D O I
10.1016/S0925-4439(97)00086-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We determined the DNA sequence of the adenylosuccinate lyase (ASL) gene from a 13 year-old female, who showed a reduced ASL enzymatic activity in lymphocytes and red blood cells and suffered from severe psychomotor retardation. The patient was the offspring of a non-consanguineous marriage. She was found to be compound heterozygous for two missense-mutations located on different alleles (C-300-G and G(1266)-T): the first mutation replaces Pro75 by Ala, the second mutation replaces Asp397 by Tyr. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:81 / 84
页数:4
相关论文
共 14 条
[1]  
AIMI J, 1990, J BIOL CHEM, V265, P9011
[2]   PURIFICATION OF ADENYLOSUCCINATE LYASE FROM RAT SKELETAL-MUSCLE BY A NOVEL AFFINITY COLUMN - STABILIZATION OF THE ENZYME, AND EFFECTS OF ANIONS AND FLUORO ANALOGS OF THE SUBSTRATE [J].
CASEY, PJ ;
LOWENSTEIN, JM .
BIOCHEMICAL JOURNAL, 1987, 246 (02) :263-269
[3]   OPTIMAL CONDITIONS FOR SIMULTANEOUS PURIFICATION OF MONONUCLEAR AND POLYMORPHONUCLEAR LEUKOCYTES FROM HUMAN-BLOOD BY THE HYPAQUE-FICOLL METHOD [J].
FERRANTE, A ;
THONG, YH .
JOURNAL OF IMMUNOLOGICAL METHODS, 1980, 36 (02) :109-117
[4]  
GOURJOIN C, 1994, COMPUT APPL BIOSCI, V11, P681
[5]   ADENYLOSUCCINASE DEFICIENCY - AN INBORN ERROR OF PURINE NUCLEOTIDE SYNTHESIS [J].
JAEKEN, J ;
WADMAN, SK ;
DURAN, M ;
VANSPRANG, FJ ;
BEEMER, FA ;
HOLL, RA ;
THEUNISSEN, PM ;
DECOCK, P ;
VANDENBERGH, F ;
VINCENT, MF ;
VANDENBERGHE, G .
EUROPEAN JOURNAL OF PEDIATRICS, 1988, 148 (02) :126-131
[6]  
JAEKEN J, 1984, LANCET, V2, P1058
[7]   CONGENITAL ADRENAL-HYPERPLASIA DUE TO POINT MUTATIONS IN THE TYPE-II 3-BETA-HYDROXYSTEROID DEHYDROGENASE GENE [J].
RHEAUME, E ;
SIMARD, J ;
MOREL, Y ;
MEBARKI, F ;
ZACHMANN, M ;
FOREST, MG ;
NEW, MI ;
LABRIE, F .
NATURE GENETICS, 1992, 1 (04) :239-245
[8]   ADENYLOSUCCINASE DEFICIENCY - A PATIENT WITH IMPAIRED ERYTHROCYTE ACTIVITY AND ANOMALOUS RESPONSE TO INTRAVENOUS FRUCTOSE [J].
SALERNO, C ;
CRIFO, C ;
GIARDINI, O .
JOURNAL OF INHERITED METABOLIC DISEASE, 1995, 18 (05) :602-608
[9]   Failure of muscle energy metabolism in a patient with adenylsuccinate lyase deficiency - An in vivo study by phosphorus NMR spectroscopy [J].
Salerno, C ;
Iotti, S ;
Lodi, R ;
Crifo, C ;
Barbiroli, B .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1997, 1360 (03) :271-276
[10]  
Sambrook J., 2002, MOL CLONING LAB MANU