Literature DB >> 2912884

Localization of Y chromosome sequences and X chromosomal replication studies in XX males.

W Schempp1, G Müller, G Scherer, S K Bohlander, W Rommerskirch, M Fraccaro, U Wolf.   

Abstract

By in situ hybridization, Y-specific DNA sequences were localized on Xp22.3-Xpter of one of the two X chromosomes in all of eleven XX males studied. In nine of the cases the presence of the Y-specific DNA did not affect random X inactivation in fibroblasts. Fibroblasts of the other two cases showed a preferential inactivation of the Y DNA-carrying X chromosome. In only one of these two exceptions blood lymphocytes could also be studied, and here, random inactivation of the Y DNA-carrying X chromosome occurred. Furthermore, the gene dosage of steroid sulfatase (STS) was examined by Southern blot analysis. In ten of the cases including the one showing random X-inactivation in lymphocytes but not in fibroblasts, a double dosage of the STS gene is present. The remaining case with non-random inactivation shows a single STS gene dosage. This case was reported previously to have STS enzyme activity in the male range. It is assumed that, as a consequence DNA sequences may result in the preferential inactivation of the Y DNA-carrying X chromosome.

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Year:  1989        PMID: 2912884     DOI: 10.1007/BF00293890

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


  38 in total

1.  A sex chromosome rearrangement in a human XX male caused by Alu-Alu recombination.

Authors:  F Rouyer; M C Simmler; D C Page; J Weissenbach
Journal:  Cell       Date:  1987-11-06       Impact factor: 41.582

2.  Investigation of three XX males by cytogenetic and DNA analyses. Suggestion of Y chromosome inversion polymorphism.

Authors:  K B Nielsen; M Schwartz; H Sardemann
Journal:  Hum Genet       Date:  1988-02       Impact factor: 4.132

3.  Analysis of two 47,XXX males reveals X-Y interchange and maternal or paternal nondisjunction.

Authors:  G Scherer; W Schempp; M Fraccaro; E Bausch; V Bigozzi; P Maraschio; E Montali; G Simoni; U Wolf
Journal:  Hum Genet       Date:  1989-02       Impact factor: 4.132

4.  Letter: Possible evidence for Xp plus in and XX Male.

Authors:  K Madan; S Walker
Journal:  Lancet       Date:  1974-06-15       Impact factor: 79.321

5.  A gradient of sex linkage in the pseudoautosomal region of the human sex chromosomes.

Authors:  F Rouyer; M C Simmler; C Johnsson; G Vergnaud; H J Cooke; J Weissenbach
Journal:  Nature       Date:  1986 Jan 23-29       Impact factor: 49.962

6.  Exchange of terminal portions of X- and Y-chromosomal short arms in human XX males.

Authors:  D C Page; L G Brown; A de la Chapelle
Journal:  Nature       Date:  1987 Jul 30-Aug 5       Impact factor: 49.962

7.  A pseudoautosomal gene in man.

Authors:  P J Goodfellow; S M Darling; N S Thomas; P N Goodfellow
Journal:  Science       Date:  1986-11-07       Impact factor: 47.728

8.  The etiology of maleness in XX men.

Authors:  A de la Chapelle
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

9.  Absence of Y-specific DNA sequences in human 46,XX true hermaphrodites and in 45,X mixed gonadal dysgenesis.

Authors:  F Waibel; G Scherer; M Fraccaro; T W Hustinx; J Weissenbach; J Wieland; A Mayerová; E Back; U Wolf
Journal:  Hum Genet       Date:  1987-08       Impact factor: 4.132

10.  Genetic heterogeneity of steroid sulfatase deficiency revealed with cDNA for human steroid sulfatase.

Authors:  J T Conary; G Lorkowski; B Schmidt; R Pohlmann; G Nagel; H E Meyer; C Krentler; J Cully; A Hasilik; K von Figura
Journal:  Biochem Biophys Res Commun       Date:  1987-04-29       Impact factor: 3.575

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  9 in total

1.  Incomplete masculinisation of XX subjects carrying the SRY gene on an inactive X chromosome.

Authors:  K Kusz; M Kotecki; A Wojda; M Szarras-Czapnik; A Latos-Bielenska; A Warenik-Szymankiewicz; A Ruszczynska-Wolska; J Jaruzelska
Journal:  J Med Genet       Date:  1999-06       Impact factor: 6.318

2.  Molecular cytogenetic analysis of XX males using Y-specific DNA sequences, including SRY.

Authors:  B Van der Auwera; N Van Roy; A De Paepe; J R Hawkins; I Liebaers; S Castedo; J Dumon; F Speleman
Journal:  Hum Genet       Date:  1992-04       Impact factor: 4.132

3.  Molecular, cytogenetic, and clinical characterisation of six XX males including one prenatal diagnosis.

Authors:  E Margarit; A Soler; A Carrió; R Oliva; D Costa; T Vendrell; J Rosell; F Ballesta
Journal:  J Med Genet       Date:  1998-09       Impact factor: 6.318

4.  Long-range restriction map of the terminal part of the short arm of the human X chromosome.

Authors:  C Petit; J Levilliers; J Weissenbach
Journal:  Proc Natl Acad Sci U S A       Date:  1990-05       Impact factor: 11.205

5.  Analysis of two 47,XXX males reveals X-Y interchange and maternal or paternal nondisjunction.

Authors:  G Scherer; W Schempp; M Fraccaro; E Bausch; V Bigozzi; P Maraschio; E Montali; G Simoni; U Wolf
Journal:  Hum Genet       Date:  1989-02       Impact factor: 4.132

6.  A ZFY-negative 46,XX true hermaphrodite is positive for the Y pseudoautosomal boundary.

Authors:  R J Jäger; C Ebensperger; M Fraccaro; G Scherer
Journal:  Hum Genet       Date:  1990-10       Impact factor: 4.132

7.  A complex rearrangement associated with sex reversal and the Wolf-Hirschhorn syndrome: a cytogenetic and molecular study.

Authors:  K Coles; M Mackenzie; J Crolla; J Harvey; J Starr; F Howard; P Jacobs
Journal:  J Med Genet       Date:  1992-06       Impact factor: 6.318

8.  Genetic characterization of two 46,XX males without gonadal ambiguities.

Authors:  Agata Minor; Fawziah Mohammed; Alla Farouk; Chiho Hatakeyama; Karynn Johnson; Victor Chow; Sai Ma
Journal:  J Assist Reprod Genet       Date:  2008-10-30       Impact factor: 3.412

9.  Steroid sulfatase gene in XX males.

Authors:  T K Mohandas; H J Stern; C A Meeker; M B Passage; U Müller; D C Page; P H Yen; L J Shapiro
Journal:  Am J Hum Genet       Date:  1990-02       Impact factor: 11.025

  9 in total

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