Literature DB >> 6321326

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

M Purrello, R Nussbaum, A Rinaldi, G Filippi, S Traccis, B Latte, M Siniscalco.   

Abstract

A Sardinian pedigree described in 1964 for having been found to segregate at the X-linked loci for the Xga antigen, G6PD deficiency, Protan and Deutan color blindness, with an instance of recombination between the last two loci, was re-examined with respect to four common X-linked DNA polymorphisms detected by molecular probes homologous to critical subregions of the human X chromosome. Two branches of this pedigree--including the one with the Protan-Deutan recombinant--were found to segregate also for the common BamHI polymorphism identified with the cDNA probe pHPT-2 or the HPRT gene (Xq26). The analysis of the chromosome haplotypes in the male offspring of the phase known penta-heterozygous mother suggests that the probable order of the relevant loci is HPRT, Deutan, G6PD, Protan, Xq telomere. Though we are fully aware of the risks of generalizing the significance of observations made on a single exceptional pedigree, we believe that this report outlines the potential of families of the type described as research tools to resolve the linear order of tightly X-linked loci and to investigate the biology of genetic recombination in humans.

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Year:  1984        PMID: 6321326     DOI: 10.1007/bf00286521

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  18 in total

1.  Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I.

Authors:  P W Rigby; M Dieckmann; C Rhodes; P Berg
Journal:  J Mol Biol       Date:  1977-06-15       Impact factor: 5.469

2.  Linkage disequilibrium for two X-linked genes in Sardinia and its bearing on the statistical mapping of the human X chromosome.

Authors:  G Filippi; A Rinaldi; R Palmarino; E Seravalli; M Siniscalco
Journal:  Genetics       Date:  1977-05       Impact factor: 4.562

3.  Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.

Authors:  L M Kunkel; K D Smith; S H Boyer; D S Borgaonkar; S S Wachtel; O J Miller; W R Breg; H W Jones; J M Rary
Journal:  Proc Natl Acad Sci U S A       Date:  1977-03       Impact factor: 11.205

4.  Failure to detect linkage between Xg and other X-borne loci in Sardinians.

Authors:  M Siniscalco; G Filippi; B Latte; S Piomelli; M Rattazzi; J Gavin; R Sanger; R R Race
Journal:  Ann Hum Genet       Date:  1966-03       Impact factor: 1.670

5.  Genetic mapping: X chromosome.

Authors:  B Keats
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

6.  Direct hybridization of labeled DNA to DNA in agarose gels.

Authors:  M Purrello; I Balazs
Journal:  Anal Biochem       Date:  1983-02-01       Impact factor: 3.365

7.  Isolation of high-molecular-weight DNA from mammalian cells.

Authors:  M Gross-Bellard; P Oudet; P Chambon
Journal:  Eur J Biochem       Date:  1973-07-02

8.  Cloned cDNA sequences of the hypoxanthine/guanine phosphoribosyltransferase gene from a mouse neuroblastoma cell line found to have amplified genomic sequences.

Authors:  J Brennand; A C Chinault; D S Konecki; D W Melton; C T Caskey
Journal:  Proc Natl Acad Sci U S A       Date:  1982-03       Impact factor: 11.205

9.  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

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

Authors:  R L Nussbaum; W E Crowder; W L Nyhan; C T Caskey
Journal:  Proc Natl Acad Sci U S A       Date:  1983-07       Impact factor: 11.205

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  3 in total

1.  Linkage analysis using multiple Xq DNA polymorphisms in normal families, families with the fragile X syndrome, and other families with X linked conditions.

Authors:  J M Connor; L A Pirrit; J R Yates; J A Crossley; S J Imrie; J M Colgan
Journal:  J Med Genet       Date:  1987-01       Impact factor: 6.318

2.  Molecular basis of abnormal red-green color vision: a family with three types of color vision defects.

Authors:  M Drummond-Borg; S Deeb; A G Motulsky
Journal:  Am J Hum Genet       Date:  1988-11       Impact factor: 11.025

3.  Structural analysis of the X-linked gene encoding human glucose 6-phosphate dehydrogenase.

Authors:  G Martini; D Toniolo; T Vulliamy; L Luzzatto; R Dono; G Viglietto; G Paonessa; M D'Urso; M G Persico
Journal:  EMBO J       Date:  1986-08       Impact factor: 11.598

  3 in total

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