In:
Journal of Inherited Metabolic Disease, Wiley, Vol. 35, No. 1 ( 2012-01), p. 133-140
Abstract:
The urea cycle defect argininosuccinate lyase (ASL) deficiency has a large spectrum of presentations from highly severe to asymptomatic. Enzyme activity assays in red blood cells or fibroblasts, although diagnostic of the deficiency, fail to discriminate between severe, mild or asymptomatic cases. Mutation/phenotype correlation studies are needed to characterize the effects of individual mutations on the activity of the enzyme. Methods Bacterial in ‐ vitro expression studies allowed the enzyme analysis of purified mutant ASL proteins p.I100T (c.299 T 〉 C), p.V178M (c.532 G 〉 A), p.E189G (c.566A 〉 G), p.Q286R (c.857A 〉 G), p.K315E (c.943A 〉 G), p.R379C (c.1135 C 〉 T) and p.R385C (c.1153 C 〉 T) in comparison to the wildtype protein. Results In the bacterial in ‐ vitro expression system, ASL wild‐type protein was successfully expressed. The known classical p.Q286R, the novel classical p.K315E and the known mutations p.I100T, p.E189G and p.R385C, which all have been linked to a mild phenotype, showed no significant residual activity. There was some enzyme activity detected with the p.V178M (5 % of wild‐type) and p.R379C (10 % of wild‐type) mutations in which K m values for argininosuccinic acid differed significantly from the wild‐type ASL protein. Conclusion The bacterially expressed enzymes proved that the mutations found in patients and studied here indeed are detrimental. However, as in the case of red cell ASL activity assays, some mutations found in genetically homozygous patients with mild presentations resulted in virtual loss of enzyme activity in the bacterial system, suggesting a more protective environment for the mutant enzyme in the liver than in the heterologous expression system and/or in the highly dilute assays utilized here.
Type of Medium:
Online Resource
ISSN:
0141-8955
,
1573-2665
DOI:
10.1007/s10545-011-9357-x
Language:
English
Publisher:
Wiley
Publication Date:
2012
detail.hit.zdb_id:
2006875-X
