Literature DB >> 6306659

A three-allele restriction-fragment-length polymorphism at the hypoxanthine phosphoribosyltransferase locus in man.

R L Nussbaum, W E Crowder, W L Nyhan, C T Caskey.   

Abstract

Using cloned cDNA sequences of murine and human hypoxanthine phosphoribosyltransferase (HPRT: IMP: pyrophosphate phosphoribosyltransferase, EC 2.4.2.8), we have identified and characterized a three-allele restriction-fragment-length polymorphism for the restriction endonuclease BamHI at the human HPRT locus. The alleles are expressed phenotypically on Southern blots as three distinct pairs of fragments that hybridize to HPRT cDNA: (i) a 22-kilobase (kb)/25-kb pair, (ii) a 12-kb/25-kb pair, and (iii) a 22-kb/18-kb pair. In addition to fragments from the HPRT locus, sequences recognized by both HPRT cDNA probes are also present on at least two autosomes in the human genome. Allele frequencies in an unselected Caucasian population are 0.77 for the 22-kb/25-kb allele. 0.16 for the 12-kb/25-kb allele, and 0.07 for the 22-kb/18-kb allele, resulting in an average heterozygosity of 38% in females in this population. This polymorphism should facilitate gene mapping by linkage in this region of the human X chromosome.

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Year:  1983        PMID: 6306659      PMCID: PMC394195          DOI: 10.1073/pnas.80.13.4035

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


  26 in total

1.  Genetic linkage between the HL-A system and a deficit of the second component (C2) of complement.

Authors:  K P Wolski; F R Schmid; K K Mittal
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2.  Detection of specific sequences among DNA fragments separated by gel electrophoresis.

Authors:  E M Southern
Journal:  J Mol Biol       Date:  1975-11-05       Impact factor: 5.469

3.  The transfer and stable integration of the HSV thymidine kinase gene into mouse cells.

Authors:  A Pellicer; M Wigler; R Axel; S Silverstein
Journal:  Cell       Date:  1978-05       Impact factor: 41.582

4.  Detection of heterozygous carriers of the Lesch-Nyhan syndrome by electrophoresis of hair root lysates.

Authors:  U Francke; B Bakay; W L Nyhan
Journal:  J Pediatr       Date:  1973-03       Impact factor: 4.406

5.  Differential staining of human and mouse chromosomes in interspecific cell hybrids.

Authors:  M Bobrow; J Cross
Journal:  Nature       Date:  1974-09-06       Impact factor: 49.962

6.  Confirmation of linkage of the loci for myotonic dystrophy and ABH secretion.

Authors:  J H Renwick; S E Bundey; M A Ferguson-Smith; M M Izatt
Journal:  J Med Genet       Date:  1971-12       Impact factor: 6.318

7.  Polymorphism of DNA sequence adjacent to human beta-globin structural gene: relationship to sickle mutation.

Authors:  Y W Kan; A M Dozy
Journal:  Proc Natl Acad Sci U S A       Date:  1978-11       Impact factor: 11.205

8.  8-Azaguanine resistance in mammalian cells. I. Hypoxanthine-guanine phosphoribosyltransferase.

Authors:  F D Gillin; D J Roufa; A L Beaudet; C T Caskey
Journal:  Genetics       Date:  1972-10       Impact factor: 4.562

9.  Myotonic dystrophy: opportunities for prenatal prediction.

Authors:  H G Schrott; G S Omenn
Journal:  Neurology       Date:  1975-08       Impact factor: 9.910

10.  Spinocerebellar ataxia and HLA linkage: risk prediction by HLA typing.

Authors:  J F Jackson; R D Currier; P I Terasaki; N E Morton
Journal:  N Engl J Med       Date:  1977-05-19       Impact factor: 91.245

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  36 in total

1.  A TaqI RFLP in the region of the HPRT locus.

Authors:  P Renwick; M Raybould; A Birley; M Hultén
Journal:  Nucleic Acids Res       Date:  1991-08-25       Impact factor: 16.971

2.  Real-time PCR and linkage studies to identify carriers presenting HPRT deleted gene.

Authors:  Cristina Lapucci; Diego Pomarè Montin; Massimo Pandolfo; Matteo Bertelli
Journal:  Mol Med       Date:  2006 Sep-Oct       Impact factor: 6.354

3.  Lesch-Nyhan syndrome: molecular investigation of three French Canadian families using a hypoxanthine-guanine phosphoribosyltransferase cDNA probe.

Authors:  D Sinnett; L Lavergne; S B Melançon; L Dallaire; M Potier; D Labuda
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

4.  Stable episomal maintenance of yeast artificial chromosomes in human cells.

Authors:  K Simpson; A McGuigan; C Huxley
Journal:  Mol Cell Biol       Date:  1996-09       Impact factor: 4.272

Review 5.  Advances in the study of inherited metabolic disease.

Authors:  D A Gibbs
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

6.  The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency.

Authors:  I Oberlé; D Drayna; G Camerino; R White; J L Mandel
Journal:  Proc Natl Acad Sci U S A       Date:  1985-05       Impact factor: 11.205

Review 7.  Molecular genetics of the human X chromosome.

Authors:  K E Davies
Journal:  J Med Genet       Date:  1985-08       Impact factor: 6.318

8.  The anonymous polymorphic DNA clone D1S1, previously mapped to human chromosome 1p36 by in situ hybridization, is from chromosome 3 and is duplicated on chromosome 1.

Authors:  M E Goode; P vanTuinen; D H Ledbetter; S P Daiger
Journal:  Am J Hum Genet       Date:  1986-04       Impact factor: 11.025

9.  Restriction site polymorphism in the phosphoglycerate kinase gene on the X chromosome.

Authors:  M H Hutz; A M Michelson; S E Antonarakis; S H Orkin; H H Kazazian
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

10.  Old and new genetics help ordering loci at the telomere of the human X-chromosome long arm.

Authors:  M Purrello; R Nussbaum; A Rinaldi; G Filippi; S Traccis; B Latte; M Siniscalco
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

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