Literature DB >> 16167093

Brief report: non-random X chromosome inactivation in females with autism.

Z Talebizadeh1, D C Bittel, O J Veatch, N Kibiryeva, M G Butler.   

Abstract

Autism is a heterogeneous neurodevelopmental disorder with a 3-4 times higher sex ratio in males than females. X chromosome genes may contribute to this higher sex ratio through unusual skewing of X chromosome inactivation. We studied X chromosome skewness in 30 females with classical autism and 35 similarly aged unaffected female siblings as controls using the polymorphic androgen receptor (AR) gene. Significantly, increased X chromosome skewness (e.g., >80:20%) was detected in our autism group (33%) compared to unaffected females (11%). X chromosome skewness was also seen in 50% of the mothers with autistic daughters. No mutation was seen in the promoter region of the XIST gene reported to be involved in X chromosome inactivation in our subjects. X chromosome skewness has been reported in female carriers of other neurological disorders such as X-linked mental retardation, adrenoleukodystrophy and Rett syndrome.

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Year:  2005        PMID: 16167093      PMCID: PMC6744835          DOI: 10.1007/s10803-005-0011-z

Source DB:  PubMed          Journal:  J Autism Dev Disord        ISSN: 0162-3257


  29 in total

1.  Nonrandom X inactivation and selection of fragile X full mutation in fetal fibroblasts.

Authors:  Y J Sun; A Baumer
Journal:  Am J Med Genet       Date:  1999-09-10

2.  Extremely skewed X-chromosome inactivation is increased in women with recurrent spontaneous abortion.

Authors:  K K Sangha; M D Stephenson; C J Brown; W P Robinson
Journal:  Am J Hum Genet       Date:  1999-09       Impact factor: 11.025

3.  X inactivation as a mechanism of selection against lethal alleles: further investigation of incontinentia pigmenti and X linked lymphoproliferative disease.

Authors:  A Harris; J Collins; D Vetrie; C Cole; M Bobrow
Journal:  J Med Genet       Date:  1992-09       Impact factor: 6.318

4.  Heritability of X chromosome--inactivation phenotype in a large family.

Authors:  A K Naumova; R M Plenge; L M Bird; M Leppert; K Morgan; H F Willard; C Sapienza
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

5.  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

6.  The human XIST gene: analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus.

Authors:  C J Brown; B D Hendrich; J L Rupert; R G Lafrenière; Y Xing; J Lawrence; H F Willard
Journal:  Cell       Date:  1992-10-30       Impact factor: 41.582

7.  A genomewide screen of 345 families for autism-susceptibility loci.

Authors:  Amanda L Yonan; Maricela Alarcón; Rong Cheng; Patrik K E Magnusson; Sarah J Spence; Abraham A Palmer; Adina Grunn; Suh-Hang Hank Juo; Joseph D Terwilliger; Jianjun Liu; Rita M Cantor; Daniel H Geschwind; T Conrad Gilliam
Journal:  Am J Hum Genet       Date:  2003-09-17       Impact factor: 11.025

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.  Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders.

Authors:  C Lord; M Rutter; A Le Couteur
Journal:  J Autism Dev Disord       Date:  1994-10

Review 10.  Non-random X chromosome inactivation in mammalian cells.

Authors:  B R Migeon
Journal:  Cytogenet Cell Genet       Date:  1998
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  27 in total

1.  X chromosome inactivation in women with alcoholism.

Authors:  Ann M Manzardo; Rebecca Henkhaus; Brandon Hidaka; Elizabeth C Penick; Albert B Poje; Merlin G Butler
Journal:  Alcohol Clin Exp Res       Date:  2012-02-29       Impact factor: 3.455

2.  X-chromosome genetic association test accounting for X-inactivation, skewed X-inactivation, and escape from X-inactivation.

Authors:  Jian Wang; Robert Yu; Sanjay Shete
Journal:  Genet Epidemiol       Date:  2014-07-08       Impact factor: 2.135

3.  Prevalence of Novel MAGED2 Mutations in Antenatal Bartter Syndrome.

Authors:  Anne Legrand; Cyrielle Treard; Isabelle Roncelin; Sophie Dreux; Aurélia Bertholet-Thomas; Françoise Broux; Daniele Bruno; Stéphane Decramer; Georges Deschenes; Djamal Djeddi; Vincent Guigonis; Nadine Jay; Tackwa Khalifeh; Brigitte Llanas; Denis Morin; Gilles Morin; François Nobili; Christine Pietrement; Amélie Ryckewaert; Rémi Salomon; Isabelle Vrillon; Anne Blanchard; Rosa Vargas-Poussou
Journal:  Clin J Am Soc Nephrol       Date:  2017-11-16       Impact factor: 8.237

4.  X inactivation in a mammal species with three sex chromosomes.

Authors:  Frédéric Veyrunes; Julie Perez
Journal:  Chromosoma       Date:  2017-12-18       Impact factor: 4.316

5.  Skewed X inactivation and IVF-conceived infants.

Authors:  Jennifer L King; Baoli Yang; Amy E T Sparks; Lindsay M Mains; Jeffrey C Murray; Bradley J Van Voorhis
Journal:  Reprod Biomed Online       Date:  2010-02-01       Impact factor: 3.828

6.  DNA methylation assay for X-chromosome inactivation in female human iPS cells.

Authors:  Lesli A Kiedrowski; Gordana Raca; Jennifer J Laffin; Benjamin S Nisler; Kimberly Leonhard; Erik McIntire; Karen Dyer Mongomery
Journal:  Stem Cell Rev Rep       Date:  2011-11       Impact factor: 5.739

7.  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

Review 8.  A review of the role of female gender in autism spectrum disorders.

Authors:  Melissa Kirkovski; Peter G Enticott; Paul B Fitzgerald
Journal:  J Autism Dev Disord       Date:  2013-11

9.  Paternally biased X inactivation in mouse neonatal brain.

Authors:  Xu Wang; Paul D Soloway; Andrew G Clark
Journal:  Genome Biol       Date:  2010-07-27       Impact factor: 13.583

10.  Is gestation in Prader-Willi syndrome affected by the genetic subtype?

Authors:  Merlin G Butler; Jennifer Sturich; Susan E Myers; June-Anne Gold; Virginia Kimonis; Daniel J Driscoll
Journal:  J Assist Reprod Genet       Date:  2009-09-17       Impact factor: 3.412

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