Literature DB >> 16647851

Random X-chromosome inactivation: skewing lessons for mice and men.

Philippe Clerc1, Philip Avner.   

Abstract

The mammalian X-chromosome exists in two flavors, active and inactive, in each cell of the adult female. This phenomenon originates from the process of random choice occurring early in development in a small number of progenitor cells in which the decision is made to inactivate either one or the other X chromosome on a cell-autonomous basis. Once made, this initial decision is irreversible, although exceptions exist in specific chromosomal territories and cell lineages. Recent findings implicate various factors, including non-coding RNAs and chromatin modification complexes, as effectors in the initiation and maintenance of X-chromosome inactivation. The functional redundancy of such factors almost certainly plays an important role in the stability of the inactive X. Studying skewing or bias opens an important opportunity for understanding facets of the random choice process.

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Year:  2006        PMID: 16647851     DOI: 10.1016/j.gde.2006.04.001

Source DB:  PubMed          Journal:  Curr Opin Genet Dev        ISSN: 0959-437X            Impact factor:   5.578


  12 in total

1.  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

2.  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

Review 3.  Using next-generation RNA sequencing to identify imprinted genes.

Authors:  X Wang; A G Clark
Journal:  Heredity (Edinb)       Date:  2014-03-12       Impact factor: 3.821

4.  A locus for familial skewed X chromosome inactivation maps to chromosome Xq25 in a family with a female manifesting Lowe syndrome.

Authors:  Milena Cau; Maria Addis; Rita Congiu; Cristiana Meloni; Antonio Cao; Simona Santaniello; Mario Loi; Francesco Emma; Orsetta Zuffardi; Roberto Ciccone; Gabriella Sole; Maria Antonietta Melis
Journal:  J Hum Genet       Date:  2006-09-06       Impact factor: 3.172

5.  Favorably skewed X-inactivation accounts for neurological sparing in female carriers of Menkes disease.

Authors:  V Desai; A Donsante; K J Swoboda; M Martensen; J Thompson; S G Kaler
Journal:  Clin Genet       Date:  2011-02       Impact factor: 4.438

Review 6.  X chromosome regulation: diverse patterns in development, tissues and disease.

Authors:  Xinxian Deng; Joel B Berletch; Di K Nguyen; Christine M Disteche
Journal:  Nat Rev Genet       Date:  2014-04-15       Impact factor: 53.242

7.  Age-dependent disease expression determines remodeling of the retinal mosaic in carriers of RPGR exon ORF15 mutations.

Authors:  William A Beltran; Gregory M Acland; Gustavo D Aguirre
Journal:  Invest Ophthalmol Vis Sci       Date:  2009-02-28       Impact factor: 4.799

8.  Chromosome territories, X;Y translocation and Premature Ovarian Failure: is there a relationship?

Authors:  Sara Lissoni; Simona Baronchelli; Nicoletta Villa; Valeria Lucchini; Enrico Betri; Pietro Cavalli; Leda Dalprà
Journal:  Mol Cytogenet       Date:  2009-09-27       Impact factor: 2.009

Review 9.  X-chromosome regulation and sex differences in brain anatomy.

Authors:  Armin Raznahan; Christine M Disteche
Journal:  Neurosci Biobehav Rev       Date:  2020-11-07       Impact factor: 8.989

10.  Sex-differential selection and the evolution of X inactivation strategies.

Authors:  Tim Connallon; Andrew G Clark
Journal:  PLoS Genet       Date:  2013-04-18       Impact factor: 5.917

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