BIOCHEMICAL-CHARACTERIZATION OF MUTANT PROPIONYL COA CARBOXYLASES FROM 2 MINOR GENETIC COMPLEMENTATION GROUPS

被引:10
作者
WOLF, B
机构
[1] Department of Human Genetics and Pediatrics, Medical College of Virginia, Richmond, 23298, Virginia
关键词
genetic complementation; propionic acidemia; propionyl CoA carboxylase deficiency;
D O I
10.1007/BF00502128
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 have biochemically characterized several parameters of propionyl CoA carboxylase (PCC) activity in fibroblast extracts from PCC-deficient patients belonging to the two minor genetic complementation groups, pcc B and pcc BC. Comparison of PCCs from these groups with those of the two major complementation groups, pcc A and pcc C, has demonstrated that PCCs from both the pcc B and pcc BC groups closely resemble each other as well as PCC from the pcc C group. These results further support the hypothesis that the pcc B and pcc BC lines are interallelic with respect to pcc C and consequently that the structural mutations in the PCCs from these groups involve the same subunit. © 1979 Plenum Publishing Corporation.
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页码:703 / 707
页数:5
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