Literature DB >> 3128684

Biochemical genetics of HPRT Cape Town: is the defect in the HPRT gene?

T Galloon1, E H Harley.   

Abstract

HPRT Cape Town shows low levels of purine salvage in cultured cells which is associated with the unusual property of substrate inhibition by its purine substrates in erythrocyte haemolysates. Since it is not certain that the defect is in the HPRT gene, we studied enzyme kinetics in cell-free preparations of erythrocytes and transformed lymphoblasts from both the proband and his obligate heterozygote daughter and studied purine salvage in intact cells. Substrate inhibition was demonstrated in erythrocyte and lymphoblast cell-free extracts from the proband and his daughter and lymphoblasts from the daughter showed similar growth properties in selective media to her father. These results were all consistent with the defect being in the HPRT gene.

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Year:  1988        PMID: 3128684     DOI: 10.1007/bf01800061

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  26 in total

1.  Statistical estimations in enzyme kinetics.

Authors:  G N WILKINSON
Journal:  Biochem J       Date:  1961-08       Impact factor: 3.857

2.  Hypoxanthine phosphoribosyltransferase activity in normal, developing, and neoplastic tissues of the rat.

Authors:  R M Wohlhueter
Journal:  Eur J Cancer       Date:  1975-07       Impact factor: 9.162

3.  Demonstration of the heterozygous state in Hunter's syndrome.

Authors:  C W Booth; H L Nadler
Journal:  Pediatrics       Date:  1974-03       Impact factor: 7.124

4.  A specific enzyme defect in gout associated with overproduction of uric acid.

Authors:  W N Kelley; F M Rosenbloom; J F Henderson; J E Seegmiller
Journal:  Proc Natl Acad Sci U S A       Date:  1967-06       Impact factor: 11.205

5.  Intracellular activity of HPRT Cape Town: purine uptake and growth of cultured cells in selective media.

Authors:  L M Steyn; E H Harley
Journal:  J Inherit Metab Dis       Date:  1985       Impact factor: 4.982

6.  Molecular evidence for new mutation at the hprt locus in Lesch-Nyhan patients.

Authors:  T P Yang; P I Patel; A C Chinault; J T Stout; L G Jackson; B M Hildebrand; C T Caskey
Journal:  Nature       Date:  1984 Aug 2-8       Impact factor: 49.962

7.  Human hypoxanthine-guanine phosphoribosyltransferase. Demonstration of structural variants in lymphoblastoid cells derived from patients with a deficiency of the enzyme.

Authors:  J M Wilson; B W Baugher; P M Mattes; P E Daddona; W N Kelley
Journal:  J Clin Invest       Date:  1982-03       Impact factor: 14.808

8.  Human hypoxanthine-guanine phosphoribosyltransferase.

Authors:  J M Wilson; R Kobayashi; I H Fox; W N Kelley
Journal:  J Biol Chem       Date:  1983-05-25       Impact factor: 5.157

9.  A molecular survey of hypoxanthine-guanine phosphoribosyltransferase deficiency in man.

Authors:  J M Wilson; J T Stout; T D Palella; B L Davidson; W N Kelley; C T Caskey
Journal:  J Clin Invest       Date:  1986-01       Impact factor: 14.808

10.  Localization of loci for hypoxanthine phosphoribosyltransferase and glucose-6-phosphate dehydrogenase and biochemical evidence of nonrandom X chromosome expression from studies of a human X-autosome translocation.

Authors:  G S Pai; J A Sprenkle; T T Do; C E Mareni; B R Migeon
Journal:  Proc Natl Acad Sci U S A       Date:  1980-05       Impact factor: 11.205

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