Literature DB >> 12068376

Skewed X-chromosome inactivation is a common feature of X-linked mental retardation disorders.

Robert M Plenge1, Roger A Stevenson, Herbert A Lubs, Charles E Schwartz, Huntington F Willard.   

Abstract

Some deleterious X-linked mutations may result in a growth disadvantage for those cells in which the mutation, when on the active X chromosome, affects cell proliferation or viability. To explore the relationship between skewed X-chromosome inactivation and X-linked mental retardation (XLMR) disorders, we used the androgen receptor X-inactivation assay to determine X-inactivation patterns in 155 female subjects from 24 families segregating 20 distinct XLMR disorders. Among XLMR carriers, approximately 50% demonstrate markedly skewed X inactivation (i.e., patterns > or =80:20), compared with only approximately 10% of female control subjects (P<.001). Thus, skewed X inactivation is a relatively common feature of XLMR disorders. Of the 20 distinct XLMR disorders, 4 demonstrate a strong association with skewed X inactivation, since all carriers of these mutations demonstrate X-inactivation patterns > or =80:20. The XLMR mutations are present on the preferentially inactive X chromosome in all 20 informative female subjects from these families, indicating that skewing is due to selection against those cells in which the XLMR mutation is on the active X chromosome.

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Year:  2002        PMID: 12068376      PMCID: PMC384975          DOI: 10.1086/341123

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


  26 in total

Review 1.  Syndromic XLMR genes (MRXS): update 2000.

Authors:  B C Hamel; P Chiurazzi; H A Lubs
Journal:  Am J Med Genet       Date:  2000-10-23

2.  GENETIC TESTS WITH A SEX-LINKED MARKER: GLUCOSE-6-PHOSPHATE DEHYDROGENASE.

Authors:  W E NANCE
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1964

3.  Patterns of X chromosome inactivation in the Rett syndrome.

Authors:  H Y Zoghbi; A K Percy; R J Schultz; C Fill
Journal:  Brain Dev       Date:  1990       Impact factor: 1.961

4.  MECP2 is highly mutated in X-linked mental retardation.

Authors:  P Couvert; T Bienvenu; C Aquaviva; K Poirier; C Moraine; C Gendrot; A Verloes; C Andrès; A C Le Fevre; I Souville; J Steffann; V des Portes; H H Ropers; H G Yntema; J P Fryns; S Briault; J Chelly; B Cherif
Journal:  Hum Mol Genet       Date:  2001-04-15       Impact factor: 6.150

5.  PAK3 mutation in nonsyndromic X-linked mental retardation.

Authors:  K M Allen; J G Gleeson; S Bagrodia; M W Partington; J C MacMillan; R A Cerione; J C Mulley; C A Walsh
Journal:  Nat Genet       Date:  1998-09       Impact factor: 38.330

Review 6.  Monogenic causes of X-linked mental retardation.

Authors:  J Chelly; J L Mandel
Journal:  Nat Rev Genet       Date:  2001-09       Impact factor: 53.242

7.  Father-to-daughter transmission of focal dermal hypoplasia associated with nonrandom X-inactivation: support for X-linked inheritance and paternal X chromosome mosaicism.

Authors:  J L Gorski
Journal:  Am J Med Genet       Date:  1991-09-01

8.  Hemizygous expression of glucose-6-phosphate dehydrogenase in erythrocytes of heterozygotes for the Lesch-Nyhan syndrome.

Authors:  W L Nyhan; B Bakay; J D Connor; J F Marks; D K Keele
Journal:  Proc Natl Acad Sci U S A       Date:  1970-01       Impact factor: 11.205

9.  Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation.

Authors:  R C Allen; H Y Zoghbi; A B Moseley; H M Rosenblatt; J W Belmont
Journal:  Am J Hum Genet       Date:  1992-12       Impact factor: 11.025

10.  X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome: localization to Xq12-q21.31 by X inactivation and linkage analysis.

Authors:  R J Gibbons; G K Suthers; A O Wilkie; V J Buckle; D R Higgs
Journal:  Am J Hum Genet       Date:  1992-11       Impact factor: 11.025

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  76 in total

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Authors:  Elif Uz; Ismail Dolen; Atakan R Al; Tayfun Ozcelik
Journal:  Hum Genet       Date:  2006-11-07       Impact factor: 4.132

2.  Identification of developmentally specific enhancers for Tsix in the regulation of X chromosome inactivation.

Authors:  Nicholas Stavropoulos; Rebecca K Rowntree; Jeannie T Lee
Journal:  Mol Cell Biol       Date:  2005-04       Impact factor: 4.272

3.  X chromosome-inactivation patterns of 1,005 phenotypically unaffected females.

Authors:  James M Amos-Landgraf; Amy Cottle; Robert M Plenge; Mike Friez; Charles E Schwartz; John Longshore; Huntington F Willard
Journal:  Am J Hum Genet       Date:  2006-07-27       Impact factor: 11.025

4.  No evidence that skewing of X chromosome inactivation patterns is transmitted to offspring in humans.

Authors:  Véronique Bolduc; Pierre Chagnon; Sylvie Provost; Marie-Pierre Dubé; Claude Belisle; Marianne Gingras; Luigina Mollica; Lambert Busque
Journal:  J Clin Invest       Date:  2008-01       Impact factor: 14.808

Review 5.  X chromosome inactivation in clinical practice.

Authors:  Karen Helene Orstavik
Journal:  Hum Genet       Date:  2009-04-25       Impact factor: 4.132

6.  May anomalous X chromosome methylation be responsible for the spontaneous abortion of a male foetus?

Authors:  R Martínez; V Bonilla-Henao; I Ramos; F Sobrino; M Lucas; E Pintado
Journal:  J Genet       Date:  2008-12       Impact factor: 1.166

7.  Next-generation sequencing in X-linked intellectual disability.

Authors:  Andreas Tzschach; Ute Grasshoff; Stefanie Beck-Woedl; Claudia Dufke; Claudia Bauer; Martin Kehrer; Christina Evers; Ute Moog; Barbara Oehl-Jaschkowitz; Nataliya Di Donato; Robert Maiwald; Christine Jung; Alma Kuechler; Solveig Schulz; Peter Meinecke; Stephanie Spranger; Jürgen Kohlhase; Jörg Seidel; Silke Reif; Manuela Rieger; Angelika Riess; Marc Sturm; Julia Bickmann; Christopher Schroeder; Andreas Dufke; Olaf Riess; Peter Bauer
Journal:  Eur J Hum Genet       Date:  2015-02-04       Impact factor: 4.246

8.  Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair.

Authors:  Marijke Bauters; Hilde Van Esch; Michael J Friez; Odile Boespflug-Tanguy; Martin Zenker; Angela M Vianna-Morgante; Carla Rosenberg; Jaakko Ignatius; Martine Raynaud; Karen Hollanders; Karen Govaerts; Kris Vandenreijt; Florence Niel; Pierre Blanc; Roger E Stevenson; Jean-Pierre Fryns; Peter Marynen; Charles E Schwartz; Guy Froyen
Journal:  Genome Res       Date:  2008-04-02       Impact factor: 9.043

9.  Skewed X inactivation in Lesch-Nyhan disease carrier females.

Authors:  Rosa J Torres; Juan G Puig
Journal:  J Hum Genet       Date:  2017-09-14       Impact factor: 3.172

10.  Comparison of X-chromosome inactivation patterns in multiple tissues from human females.

Authors:  D C Bittel; M F Theodoro; N Kibiryeva; W Fischer; Z Talebizadeh; M G Butler
Journal:  J Med Genet       Date:  2007-12-21       Impact factor: 6.318

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