Literature DB >> 7116451

Derepression with decreased expression of the G6PD locus on the inactive X chromosome in normal human cells.

B R Migeon, S F Wolf, C Mareni, J Axelman.   

Abstract

Studies of a unique clone of skin fibroblasts from a normal 46 XX female reveal that the G6PD locus on the inactive X chromosome has been derepressed. The reactivation event occurs spontaneously, and is associated with normal karyotype, including the presence of a late-replicating X chromosome. Analysis of mouse-human hybrids with the relevant chromosome provides evidence that the derepressed locus is on the inactive X, and that reactivation is not extensive (the PGK locus is not derepressed). Nor is any general change in DNA methylation of this chromosome detectable with Hpa II and an X-specific DNA probe. Studies of the glucose-6-phosphate dehydrogenase phenotype in these heterozygous cells indicate that the reactivated X produces only half the enzyme subunits as are produced by the active X. Although this dosage difference may be related to the mutational event responsible for derepression of the locus, these observations along with other evidence suggest that loci on the inactive X, when expressed, have less activity than corresponding loci on the active X.

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Year:  1982        PMID: 7116451     DOI: 10.1016/0092-8674(82)90175-1

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  23 in total

1.  Hyperexpression of HPRT induced by 5-azacytidine in mouse-human hybrid reactivants.

Authors:  B R Migeon; G G Johnson; S F Wolf; J Axelman; M Schmidt
Journal:  Am J Hum Genet       Date:  1985-05       Impact factor: 11.025

Review 2.  The single active X in human cells: evolutionary tinkering personified.

Authors:  Barbara R Migeon
Journal:  Hum Genet       Date:  2011-06-08       Impact factor: 4.132

Review 3.  The great escape.

Authors:  C M Disteche
Journal:  Am J Hum Genet       Date:  1997-06       Impact factor: 11.025

4.  Expression of genes from the human active and inactive X chromosomes.

Authors:  C J Brown; L Carrel; H F Willard
Journal:  Am J Hum Genet       Date:  1997-06       Impact factor: 11.025

5.  Unusual (CGG)n expansion and recombination in a family with fragile X and DiGeorge syndrome.

Authors:  J N Macpherson; G Curtis; J A Crolla; N Dennis; B Migeon; P K Grewal; M C Hirst; K E Davies; P A Jacobs
Journal:  J Med Genet       Date:  1995-03       Impact factor: 6.318

Review 6.  Dosage compensation in mammals: why does a gene on the inactive X yield less product than one on the active X?

Authors:  O J Miller
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

7.  Replication variants of the human inactive X chromosome. II. Frequency and replication rate relative to the other chromosomes of the complement.

Authors:  M Schmidt; W M Stolzmann
Journal:  Chromosoma       Date:  1984       Impact factor: 4.316

8.  Differential activation of the hprt gene on the inactive X chromosome in primary and transformed Chinese hamster cells.

Authors:  S G Grant; R G Worton
Journal:  Mol Cell Biol       Date:  1989-04       Impact factor: 4.272

9.  Methylation of the hypoxanthine phosphoribosyltransferase locus on the human X chromosome: implications for X-chromosome inactivation.

Authors:  S F Wolf; D J Jolly; K D Lunnen; T Friedmann; B R Migeon
Journal:  Proc Natl Acad Sci U S A       Date:  1984-05       Impact factor: 11.205

10.  Incomplete X chromosome dosage compensation in chorionic villi of human placenta.

Authors:  B R Migeon; S F Wolf; J Axelman; D C Kaslow; M Schmidt
Journal:  Proc Natl Acad Sci U S A       Date:  1985-05       Impact factor: 11.205

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