Literature DB >> 1346076

Identification of novel RFLPs in the vicinity of CpG islands in Xq28: application to the analysis of the pattern of X chromosome inactivation.

E Maestrini1, S Rivella, C Tribioli, M Rocchi, G Camerino, S Santachiara-Benerecetti, O Parolini, L D Notarangelo, D Toniolo.   

Abstract

Probes for CpG islands were cloned from the distal long arm of the human X chromosome; three of them were found to be polymorphic. A HindIII RFLP was identified by the probe 2-25 (DXS606), and it was mapped to the Xq27-Xq28 boundary. Probes 2-19 (DXS605) and 2-55 (DXS707), which identify EcoRI and MspI polymorphisms, respectively, have been mapped to the distal part of Xq28, in the G6PD-RCP/GCP gene region. Probe 2-19 has been further localized about 16 kb from the 3' end of the G6PD gene. The new RFLPs may be useful for the precise mapping of the many disease genes localized in this part of the human X chromosome. Probe 2-19 is highly informative, and it has been studied in greater detail. Using the methylation-sensitive rare-cutter enzyme EagI in conjunction with the polymorphic EcoRI site, we were able to demonstrate that the RFLP may be used both to study randomness of X chromosome inactivation and for carrier detection in X-linked syndromes where nonrandom X inactivation occurs. It is conceivable that the combined use of 2-19 and of the probes described so far (pSPT-PGK and M27 beta) will make analysis of X inactivation feasible in virtually every female.

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Year:  1992        PMID: 1346076      PMCID: PMC1682517     

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


  23 in total

1.  The nucleotide sequence of a CpG island demonstrates the presence of the first exon of the gene encoding the human lysosomal membrane protein lamp2 and assigns the gene to Xq24.

Authors:  M Manoni; C Tribioli; B Lazzari; G DeBellis; C Patrosso; R Pergolizzi; M Pellegrini; E Maestrini; S Rivella; P Vezzoni
Journal:  Genomics       Date:  1991-03       Impact factor: 5.736

2.  Differential methylation of the hypervariable locus DXS255 on active and inactive X chromosomes correlates with the expression of a human X-linked gene.

Authors:  R M Brown; N J Fraser; G K Brown
Journal:  Genomics       Date:  1990-06       Impact factor: 5.736

3.  Probes for CpG islands on the distal long arm of the human X chromosome are clustered in Xq24 and Xq28.

Authors:  E Maestrini; S Rivella; C Tribioli; D Purtilo; M Rocchi; N Archidiacono; D Toniolo
Journal:  Genomics       Date:  1990-12       Impact factor: 5.736

Review 4.  Definition of the gene loci in X-linked immunodeficiencies.

Authors:  M E Conley; J M Puck
Journal:  Immunol Invest       Date:  1988-07       Impact factor: 3.657

5.  Active X chromosome DNA is unmethylated at eight CCGG sites clustered in a guanine-plus-cytosine-rich island at the 5' end of the gene for phosphoglycerate kinase.

Authors:  D H Keith; J Singer-Sam; A D Riggs
Journal:  Mol Cell Biol       Date:  1986-11       Impact factor: 4.272

6.  Nonrandom X chromosome inactivation in B cells from carriers of X chromosome-linked severe combined immunodeficiency.

Authors:  M E Conley; A Lavoie; C Briggs; P Brown; C Guerra; J M Puck
Journal:  Proc Natl Acad Sci U S A       Date:  1988-05       Impact factor: 11.205

7.  An extensive search for RFLP in the human glucose-6-phosphate dehydrogenase locus has revealed a silent mutation in the coding sequence.

Authors:  M D'Urso; L Luzzatto; L Perroni; A Ciccodicola; G Gentile; I Peluso; M G Persico; T Pizzella; D Toniolo; T J Vulliamy
Journal:  Am J Hum Genet       Date:  1988-05       Impact factor: 11.025

8.  Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines.

Authors:  G K Suthers; V J Hyland; D F Callen; I Oberle; M Rocchi; N S Thomas; C P Morris; C E Schwartz; M Schmidt; H H Ropers
Journal:  Am J Hum Genet       Date:  1990-08       Impact factor: 11.025

9.  Isolation of mammalian cell mutants deficient in glucose-6-phosphate dehydrogenase activity: linkage to hypoxanthine phosphoribosyl transferase.

Authors:  M Rosenstraus; L A Chasin
Journal:  Proc Natl Acad Sci U S A       Date:  1975-02       Impact factor: 11.205

10.  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

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  5 in total

1.  The QM gene is X-linked and therefore not involved in suppression of tumorigenesis in Wilms' tumor.

Authors:  A M van den Ouweland; M Verdijk; M M Mannens; B A van Oost
Journal:  Hum Genet       Date:  1992 Sep-Oct       Impact factor: 4.132

2.  Refining the genetic location of the gene for X linked hydrocephalus within Xq28.

Authors:  M Jouet; E Feldman; J Yates; D Donnai; J Paterson; D Siggers; S Kenwrick
Journal:  J Med Genet       Date:  1993-03       Impact factor: 6.318

3.  X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome.

Authors:  A K Gedeon; M J Wilson; A C Colley; D O Sillence; J C Mulley
Journal:  J Med Genet       Date:  1995-05       Impact factor: 6.318

4.  X-chromosome methylation in manifesting and healthy carriers of dystrophinopathies: concordance of activation ratios among first degree female relatives and skewed inactivation as cause of the affected phenotypes.

Authors:  J Azofeifa; T Voit; C Hübner; M Cremer
Journal:  Hum Genet       Date:  1995-08       Impact factor: 4.132

5.  Clonal analysis of human astrocytomas.

Authors:  R P Morse; B T Darras; Z Ye; J K Wu
Journal:  J Neurooncol       Date:  1994       Impact factor: 4.130

  5 in total

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