A bacterial model for expression of mutations in the human ornithine transcarbamylase (OTC) gene
Journal Article
·
· American Journal of Human Genetics
OSTI ID:134757
- Univ. of Minnesota, Mineapolis (United States)
OTC is a mitochondrial enzyme catalyzing the formation of citrulline from carbamyl phosphate and ornithine. X-linked deficiency of OTC is the most prevalent genetic defect of ureagenesis. Mutations and polymorphisms in the OTC gene identified in deficient patients have indicated the occurrence of many family-specific, unique alleles. Due to the low frequency of recurrent mutations, distinguishing between deleterious mutations and polymorphisms is difficult. Using a human OTC gene containing plasmid driven by a tac promoter, we have devised a simple and efficient method for expressing mutations in the mature human OTC enzyme. To demonstrate this method, PCR engineered site-directed mutagenesis was employed to generated cDNA fragments which contained either the R151Q or R277W known mutations found in patients with neonatal and late-onset OTC deficiency, respectively. The normal allele for each mutation was also generated by an identical PCR procedure. Digestion with Bgl II- and Sty I-generated mutant and normal replacement cassettes containing the respective mutant and wild type sequences. Upon transformation of JM109 E.coli cells, OTC enzymatic activity was measured at log and stationary phases of growth using a radiochromatographic method. The R141Q mutation abolished enzymatic activity (<0.02% of normal), whereas the R277W mutation expressed partial activity (2.3% of normal). In addition, a PCR-generated mutation, A280V, resulted in 73% loss of catalytic activity. This OTC expression system is clinically applicable for distinguishing between mutations and polymorphisms, and it can be used to investigate the effects of mutations on various domains of the OTC gene.
- OSTI ID:
- 134757
- Report Number(s):
- CONF-941009--
- Journal Information:
- American Journal of Human Genetics, Journal Name: American Journal of Human Genetics Journal Issue: Suppl.3 Vol. 55; ISSN AJHGAG; ISSN 0002-9297
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
55 BIOLOGY AND MEDICINE
BASIC STUDIES
AGE DEPENDENCE
BIOLOGICAL MODELS
EFFICIENCY
ENZYME ACTIVITY
ENZYMES
ESCHERICHIA COLI
GENE MUTATIONS
GENES
GENETICS
HEREDITARY DISEASES
HUMAN X CHROMOSOME
MITOCHONDRIA
MUTAGENESIS
MUTATION FREQUENCY
ORNITHINE
PATIENTS
POLYMERASE CHAIN REACTION
UROGENITAL SYSTEM DISEASES
BASIC STUDIES
AGE DEPENDENCE
BIOLOGICAL MODELS
EFFICIENCY
ENZYME ACTIVITY
ENZYMES
ESCHERICHIA COLI
GENE MUTATIONS
GENES
GENETICS
HEREDITARY DISEASES
HUMAN X CHROMOSOME
MITOCHONDRIA
MUTAGENESIS
MUTATION FREQUENCY
ORNITHINE
PATIENTS
POLYMERASE CHAIN REACTION
UROGENITAL SYSTEM DISEASES