Literature DB >> 6328977

The parental origin of X chromosomes in XX males determined using restriction fragment length polymorphisms.

D C Page, A de la Chapelle.   

Abstract

The inheritance of several X-linked restriction fragment length polymorphisms ( RFLPs ) is examined in seven 46,XX males and their immediate relatives. The XX males are shown to have inherited a paternal and a maternal RFLP allele in each of the five (of seven) families in which these X-linked markers are informative. In the other two families, a maternal X-chromosomal contribution is demonstrated, but a paternal contribution cannot be determined. We conclude that most, if not all, XX males inherit one paternal and one maternal X chromosome. A segment of single-copy DNA specific to the short arm of the Y chromosome is found to be absent from the genomes of eight XX males. In one of these XX males, an Xp-Yp translocation had previously been inferred from chromosome-banding studies. Our findings argue against mosaicism involving a Y-containing cell line in the XX males examined here, but they do not exclude an X-Y (or Y-autosome) translocation during paternal meiosis. If such a translocation has occurred, the translocation product received by the XX males does not include the Yp-specific sequence tested here.

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Year:  1984        PMID: 6328977      PMCID: PMC1684446     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  20 in total

1.  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

2.  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

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.  X-Y chromosomal interchange in the aetiology of true hermaphroditism and of XX Klinefelter's syndrome.

Authors:  M A Ferguson-Smith
Journal:  Lancet       Date:  1966-08-27       Impact factor: 79.321

5.  Presence of brightly fluorescent material in testes of XX males.

Authors:  W A Palutke; Y Chen; H Chen
Journal:  J Med Genet       Date:  1973-06       Impact factor: 6.318

6.  Heteromorphic X chromosomes in 46,XX males: evidence for the involvement of X-Y interchange.

Authors:  H J Evans; K E Buckton; G Spowart; A D Carothers
Journal:  Hum Genet       Date:  1979-05-23       Impact factor: 4.132

7.  Recessive sex-determining genes in human XX male syndrome.

Authors:  A de la Chapelle; G C Koo; S S Wachtel
Journal:  Cell       Date:  1978-11       Impact factor: 41.582

8.  Heteromorphic X chromosomes in 46,XX males?

Authors:  A de la Chapelle; K Simola; P Simola; S Knuutila; N Gahmberg; L Pajunen; C Lundqvist; S Sarna; J Murros
Journal:  Hum Genet       Date:  1979-11       Impact factor: 4.132

9.  Two XX males in one family and additional observations bearing on the etiology of XX males.

Authors:  A D Chapelle; J Schröder; J Murros; G Tallqvist
Journal:  Clin Genet       Date:  1977-02       Impact factor: 4.438

10.  A human quantitative polymorphism related to Xg blood groups.

Authors:  P N Goodfellow; P Tippett
Journal:  Nature       Date:  1981-01-29       Impact factor: 49.962

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  21 in total

1.  Molecular analysis of hemophilia A mutations in the Finnish population.

Authors:  B Levinson; A E Lehesjoki; A de la Chapelle; J Gitschier
Journal:  Am J Hum Genet       Date:  1990-01       Impact factor: 11.025

2.  Coincident maternal meiotic nondisjunction of chromosomes X and 21 without evidence of autosomal asynapsis.

Authors:  R S Ikonen; M Lindlöf; M O Janas; K O Simola; A Millington-Ward; A de la Chapelle
Journal:  Hum Genet       Date:  1989-10       Impact factor: 4.132

3.  Molecular characterization of a Y;15 translocation segregating in a family.

Authors:  T Alitalo; J Tiihonen; P Hakola; A de la Chapelle
Journal:  Hum Genet       Date:  1988-05       Impact factor: 4.132

4.  Characterization of a (Y;4) translocation by DNA hybridization.

Authors:  M Andersson; D C Page; L G Brown; K Elfving; A de la Chapelle
Journal:  Hum Genet       Date:  1988-04       Impact factor: 4.132

5.  Determination of the parental origin of sex-chromosome monosomy using restriction fragment length polymorphisms.

Authors:  T Hassold; E Kumlin; N Takaesu; M Leppert
Journal:  Am J Hum Genet       Date:  1985-09       Impact factor: 11.025

6.  Cystic fibrosis in Finland: a molecular and genealogical study.

Authors:  J Kere; R Norio; E Savilahti; X Estivill; A de la Chapelle
Journal:  Hum Genet       Date:  1989-08       Impact factor: 4.132

7.  XX true hermaphroditism in southern African blacks: an enigma of primary sexual differentiation.

Authors:  M Ramsay; R Bernstein; E Zwane; D C Page; T Jenkins
Journal:  Am J Hum Genet       Date:  1988-07       Impact factor: 11.025

8.  Molecular detection of a translocation (Y;15) in a 45,X male.

Authors:  C M Disteche; L Brown; H Saal; C Friedman; H C Thuline; D I Hoar; R A Pagon; D C Page
Journal:  Hum Genet       Date:  1986-12       Impact factor: 4.132

9.  An extended long-range restriction map of the human sex-determining region on Yp, including ZFY, finds marked homology on Xp and no detectable Y sequences in an XX male.

Authors:  V Verga; R P Erickson
Journal:  Am J Hum Genet       Date:  1989-05       Impact factor: 11.025

10.  A 45,X male with Y-specific DNA translocated onto chromosome 15.

Authors:  A Gal; B Weber; G Neri; A Serra; U Müller; W Schempp; D C Page
Journal:  Am J Hum Genet       Date:  1987-06       Impact factor: 11.025

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