STRUCTURAL AND EXPRESSION ANALYSES OF NORMAL AND MUTANT MESSENGER-RNA ENCODING GLYCINE DECARBOXYLASE - 3-BASE DELETION IN MESSENGER-RNA CAUSES NONKETOTIC HYPERGLYCINEMIA

被引:32
作者
KURE, S [1 ]
NARISAWA, K [1 ]
TADA, K [1 ]
机构
[1] TOHOKU UNIV,SCH MED,DEPT PEDIAT,AOBA KU,SENDAI,MIYAGI 980,JAPAN
关键词
D O I
10.1016/0006-291X(91)91545-N
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
Full-length cDNA clone encoding human glycine decarboxylase (P-protein) was isolated from the human placental λgt11 expression library using specific antibodies. This clone was 3,705 bp in length and encoded 1,020 amino acids. We studied the structure of the mutant P-protein mRNA expressed in the liver of a patient with nonketotic hyperglycinemia (NKH) deficient of P-protein. A three-base deletion, which resulted in deletion of Phe756, was found. Cos7 cells in which normal P-protein cDNA was expressed presented an activity of 6.9±0.41 nmole/milligram of protein/hour, which was almost equivalent to that of human liver. In contrast, Cos7 cells in which the mutant cDNA was expressed showed no activity, indicating that the three-base deletion could cause NKH. © 1991.
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页码:1176 / 1182
页数:7
相关论文
共 15 条
[1]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[2]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[3]   PURIFICATION AND PROPERTIES OF GLYCINE DECARBOXYLASE, A COMPONENT OF THE GLYCINE CLEAVAGE SYSTEM, FROM RAT-LIVER MITOCHONDRIA AND IMMUNOCHEMICAL COMPARISON OF THIS ENZYME FROM VARIOUS SOURCES [J].
HAYASAKA, K ;
KOCHI, H ;
HIRAGA, K ;
KIKUCHI, G .
JOURNAL OF BIOCHEMISTRY, 1980, 88 (04) :1193-1199
[4]   UNIDIRECTIONAL DIGESTION WITH EXONUCLEASE-III CREATES TARGETED BREAKPOINTS FOR DNA SEQUENCING [J].
HENIKOFF, S .
GENE, 1984, 28 (03) :351-359
[5]  
HIRAGA K, 1980, J BIOL CHEM, V255, P1664
[6]   GLYCINE CLEAVAGE SYSTEM - COMPOSITION, REACTION-MECHANISM, AND PHYSIOLOGICAL SIGNIFICANCE [J].
KIKUCHI, G .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1973, 1 (02) :169-187
[7]  
MARCEAU M, 1988, J BIOL CHEM, V263, P16926
[8]   IDENTIFICATION OF A COMMON MUTATION IN PATIENTS WITH MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY [J].
MATSUBARA, Y ;
NARISAWA, K ;
MIYABAYASHI, S ;
TADA, K ;
COATES, PM ;
BACHMANN, C ;
ELSAS, LJ ;
POLLITT, RJ ;
RHEAD, WJ ;
ROE, CR .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 171 (01) :498-505
[9]   GLYCINE METABOLISM BY RAT LIVER MITOCHONDRIA .4. ISOLATION AND CHARACTERIZATION OF HYDROGEN CARRIER PROTEIN, AN ESSENTIAL FACTOR FOR GLYCINE METABOLISM [J].
MOTOKAWA, Y ;
KIKUCHI, G .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1969, 135 (1-2) :402-&
[10]  
Nyhan W.L., 1989, METABOLIC BASIS INHE, P743