Literature DB >> 1587534

Expression of RPS4X in fibroblasts from patients with structural aberrations of the X chromosome.

W Just1, C Geerkens, K R Held, W Vogel.   

Abstract

A series of fibroblasts from patients with numerical or structural aberrations of the X chromosome were scored for the amount of mRNA of ribosomal protein S4 (RPS4X). Haplo-insufficiency of this gene has been reported previously to be a possible cause of Turner syndrome. Our results show that the transcription rate of RPS4X correlates with the number of gene copies. This confirms earlier findings indicating that this gene escapes X inactivation. In addition, we demonstrate that this applies to structurally aberrant X chromosomes. Our results show that RPS4X does not give rise to a type of haplo-insufficiency in these cases, because it escapes inactivation, even on structurally aberrant X chromosomes from patients with Turner syndrome. We therefore assume that RPS4X is not the most prominent candidate gene for Turner syndrome.

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Year:  1992        PMID: 1587534     DOI: 10.1007/bf00217131

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


  12 in total

1.  Analysis of the origin of Turner's syndrome using polymorphic DNA probes.

Authors:  S A Loughlin; A Redha; J McIver; E Boyd; A Carothers; J M Connor
Journal:  J Med Genet       Date:  1991-03       Impact factor: 6.318

2.  Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndrome.

Authors:  E M Fisher; P Beer-Romero; L G Brown; A Ridley; J A McNeil; J B Lawrence; H F Willard; F R Bieber; D C Page
Journal:  Cell       Date:  1990-12-21       Impact factor: 41.582

3.  Isolation of an abundantly expressed sequence from the human X chromosome by differential screening.

Authors:  M V Wiles; C M Alexander; P N Goodfellow
Journal:  Somat Cell Mol Genet       Date:  1988-01

4.  A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules.

Authors:  B Franco; S Guioli; A Pragliola; B Incerti; B Bardoni; R Tonlorenzi; R Carrozzo; E Maestrini; M Pieretti; P Taillon-Miller; C J Brown; H F Willard; C Lawrence; M Graziella Persico; G Camerino; A Ballabio
Journal:  Nature       Date:  1991-10-10       Impact factor: 49.962

5.  Temporal regulation of hyaluronan and proteoglycan metabolism by human bone cells in vitro.

Authors:  N S Fedarko; J D Termine; M F Young; P G Robey
Journal:  J Biol Chem       Date:  1990-07-25       Impact factor: 5.157

6.  Isolation and characterization of rat and human glyceraldehyde-3-phosphate dehydrogenase cDNAs: genomic complexity and molecular evolution of the gene.

Authors:  J Y Tso; X H Sun; T H Kao; K S Reece; R Wu
Journal:  Nucleic Acids Res       Date:  1985-04-11       Impact factor: 16.971

7.  Various rat adult tissues express only one major mRNA species from the glyceraldehyde-3-phosphate-dehydrogenase multigenic family.

Authors:  P Fort; L Marty; M Piechaczyk; S el Sabrouty; C Dani; P Jeanteur; J M Blanchard
Journal:  Nucleic Acids Res       Date:  1985-03-11       Impact factor: 16.971

8.  Localization of the X inactivation centre on the human X chromosome in Xq13.

Authors:  C J Brown; R G Lafreniere; V E Powers; G Sebastio; A Ballabio; A L Pettigrew; D H Ledbetter; E Levy; I W Craig; H F Willard
Journal:  Nature       Date:  1991-01-03       Impact factor: 49.962

9.  Localization of the human GM-CSF receptor gene to the X-Y pseudoautosomal region.

Authors:  N M Gough; D P Gearing; N A Nicola; E Baker; M Pritchard; D F Callen; G R Sutherland
Journal:  Nature       Date:  1990-06-21       Impact factor: 49.962

10.  The similarity of phenotypic effects caused by Xp and Xq deletions in the human female: a hypothesis.

Authors:  E Therman; B Susman
Journal:  Hum Genet       Date:  1990-07       Impact factor: 4.132

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  7 in total

1.  Gene for the alpha-subunit of the human interleukin-3 receptor (IL3RA) localized to the X-Y pseudoautosomal region.

Authors:  A Milatovich; T Kitamura; A Miyajima; U Francke
Journal:  Am J Hum Genet       Date:  1993-11       Impact factor: 11.025

2.  Ullrich-Turner syndrome is not caused by haploinsufficiency of RPS4X.

Authors:  C Geerkens; W Just; K R Held; W Vogel
Journal:  Hum Genet       Date:  1996-01       Impact factor: 4.132

3.  An analysis of Xq deletions.

Authors:  P Maraschio; R Tupler; L Barbierato; E Dainotti; D Larizza; F Bernardi; H Hoeller; A Garau; L Tiepolo
Journal:  Hum Genet       Date:  1996-03       Impact factor: 4.132

Review 4.  Chromosomal localisation of a gene(s) for Turner stigmata on Yp.

Authors:  T Ogata; C Tyler-Smith; S Purvis-Smith; G Turner
Journal:  J Med Genet       Date:  1993-11       Impact factor: 6.318

5.  Absence of Turner stigmata in a 46,XYp-female.

Authors:  U Müller; V G Kirkels; J M Scheres
Journal:  Hum Genet       Date:  1992-11       Impact factor: 4.132

Review 6.  Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features.

Authors:  T Ogata; N Matsuo
Journal:  Hum Genet       Date:  1995-06       Impact factor: 4.132

7.  Widespread DNA hypomethylation and differential gene expression in Turner syndrome.

Authors:  Christian Trolle; Morten Muhlig Nielsen; Anne Skakkebæk; Philippe Lamy; Søren Vang; Jakob Hedegaard; Iver Nordentoft; Torben Falck Ørntoft; Jakob Skou Pedersen; Claus Højbjerg Gravholt
Journal:  Sci Rep       Date:  2016-09-30       Impact factor: 4.379

  7 in total

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