Literature DB >> 5283941

Hypoxanthine-guanine phosphoribosyltransferase deficiency: chemical agents selective for mutant or normal cultured fibroblasts in mixed and heterozygote cultures.

W Y Fujimoto, J H Subak-Sharpe, J E Seegmiller.   

Abstract

Cultured fibroblasts established from skin biopsies from patients with the Lesch-Nyhan syndrome are deficient in hypoxanthine-guanine phosphoribosyl-transferase (EC 2.4.2.8) activity. This deficiency makes possible the use of chemicals that select either for or against deficient variants in cultured fibroblasts. Two-way selection has been achieved by the use of 6-thioguanine, which selects for the deficient mutant, and azaserine, which selects to some extent for the normal allele in mixed cultures, as well as in cultures from heterozygotes. Theoretical considerations predict that the phenomenon of metabolic cooperation would tend to reinforce the former and to weaken the latter type of selection, and this is in accordance with the experimental findings.

Entities:  

Mesh:

Substances:

Year:  1971        PMID: 5283941      PMCID: PMC389230          DOI: 10.1073/pnas.68.7.1516

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  23 in total

1.  THE INOSINIC ACID PYROPHOSPHORYLASE ACTIVITY OF MOUSE FIBROBLASTS PARTIALLY RESISTANT TO 8-AZAGUANINE.

Authors:  J W LITTLEFIELD
Journal:  Proc Natl Acad Sci U S A       Date:  1963-09       Impact factor: 11.205

2.  BIOCHEMICALLY MARKED VARIANTS OF THE SYRIAN HAMSTER FIBROBLAST CELL LINE BHK21 AND ITS DERIVATIVES.

Authors:  H SUBAK-SHARPE
Journal:  Exp Cell Res       Date:  1965-04       Impact factor: 3.905

3.  Biochemical diagnosis of an X-linked disease in utero.

Authors:  W Y Fujimoto; J E Seegmiller; B W Uhlendorf; C B Jacobson
Journal:  Lancet       Date:  1968-08-31       Impact factor: 79.321

4.  Lesch-Nyhan syndrome: preventive control by prenatal diagnosis.

Authors:  J A Boyle; K O Raivio; K H Astrin; J D Schulman; M L Graf; J E Seegmiller; C B Jacobsen
Journal:  Science       Date:  1970-08-14       Impact factor: 47.728

5.  Inheritance of purine phosphoribosyltransferases in man.

Authors:  J F Henderson; W N Kelley; F M Rosenbloom; J E Seegmiller
Journal:  Am J Hum Genet       Date:  1969-01       Impact factor: 11.025

6.  Single-allele expression at an X-linked hyperuricemia locus in heterozygous human cells.

Authors:  J Salzmann; R DeMars; P Benke
Journal:  Proc Natl Acad Sci U S A       Date:  1968-06       Impact factor: 11.205

7.  X-linked recessive inheritance of a syndrome of mental retardation with hyperuricemia.

Authors:  S L Shapiro; G L Sheppard; F E Dreifuss; D S Newcombe
Journal:  Proc Soc Exp Biol Med       Date:  1966-06

8.  Lesch-Nyhan mutation: prenatal detection with amniotic fluid cells.

Authors:  R DeMars; G Sarto; J S Felix; P Benke
Journal:  Science       Date:  1969-06-13       Impact factor: 47.728

9.  Hypoxanthine-guanine phosphoribosyltransferase deficiency: activity in normal, mutant, and heterozygote-cultured human skin fibroblasts.

Authors:  W Y Fujimoto; J E Seegmiller
Journal:  Proc Natl Acad Sci U S A       Date:  1970-03       Impact factor: 11.205

10.  Evidence for transfer of enzyme product as the basis of metabolic cooperation between tissue culture fibroblasts of Lesch-Nyhan disease and normal cells.

Authors:  R P Cox; M R Krauss; M E Balis; J Dancis
Journal:  Proc Natl Acad Sci U S A       Date:  1970-11       Impact factor: 11.205

View more
  16 in total

1.  Cytokine regulation of gap junction connectivity: an open-and-shut case or changing partners at the Nexus?

Authors:  C F Brosnan; E Scemes; D C Spray
Journal:  Am J Pathol       Date:  2001-05       Impact factor: 4.307

2.  Mosaicism of peripheral blood lymphocyte populations in females heterozygous for the Lesch-Nyhan mutation.

Authors:  R J Albertini; R DeMars
Journal:  Biochem Genet       Date:  1974-05       Impact factor: 1.890

3.  Family studies of a Lesch-Nyhan patient from an isolated Canadian community.

Authors:  K Itiaba; M Banfalvi; J C Crawhall; J G Mongeau
Journal:  Am J Hum Genet       Date:  1973-03       Impact factor: 11.025

4.  [Lesch-Nyhan syndrome. Heterozygote detection by biochemical selection of the mutant cells and autoradiography].

Authors:  A M Hagemeijer; P Dodinval; J M Andrien
Journal:  Humangenetik       Date:  1972

5.  The use of quantiatative cytochemical analyses in rapid prenatal detection and somatic cell genetic studies of metabolic diseases.

Authors:  H Galjaard; A Hoogeveen; W Keijzer; E De Wit-Verbeek; C Vlek-Noot
Journal:  Histochem J       Date:  1974-09

6.  The extent of heterocellular communication mediated by gap junctions is predictive of bystander tumor cytotoxicity in vitro.

Authors:  J Fick; F G Barker; P Dazin; E M Westphale; E C Beyer; M A Israel
Journal:  Proc Natl Acad Sci U S A       Date:  1995-11-21       Impact factor: 11.205

7.  Mutations affecting the structure of hypoxanthine: guanine phosphoribosyltransferase in cultured Chinese hamster cells.

Authors:  A L Beaudet; D J Roufa; C T Caskey
Journal:  Proc Natl Acad Sci U S A       Date:  1973-02       Impact factor: 11.205

8.  Loss of dopamine phenotype among midbrain neurons in Lesch-Nyhan disease.

Authors:  Martin Göttle; Cecilia N Prudente; Rong Fu; Diane Sutcliffe; Hong Pang; Deborah Cooper; Emir Veledar; Jonathan D Glass; Marla Gearing; Jasper E Visser; H A Jinnah
Journal:  Ann Neurol       Date:  2014-06-20       Impact factor: 10.422

9.  Consequences of impaired purine recycling in dopaminergic neurons.

Authors:  J C Lewers; I Ceballos-Picot; T L Shirley; L Mockel; K Egami; H A Jinnah
Journal:  Neuroscience       Date:  2008-01-17       Impact factor: 3.590

10.  Gap junctions and Bystander Effects: Good Samaritans and executioners.

Authors:  David C Spray; Regina Hanstein; Sandra V Lopez-Quintero; Randy F Stout; Sylvia O Suadicani; Mia M Thi
Journal:  Wiley Interdiscip Rev Membr Transp Signal       Date:  2012-12-11
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.