Literature DB >> 25558953

Behavioral phenotypes in males with XYY and possible role of increased NLGN4Y expression in autism features.

J L Ross1, N Tartaglia, D E Merry, M Dalva, A R Zinn.   

Abstract

The male sex chromosome disorder, 47,XYY syndrome (XYY), is associated with increased risk for social-emotional difficulties, attention-deficit hyperactivity disorder (ADHD) and autism spectrum disorder (ASD). We hypothesize that increased Y chromosome gene copy number in XYY leads to overexpression of Y-linked genes related to brain development and function, thereby increasing risk for these phenotypes. We measured expression in blood of two Y genes NLGN4Y and RPS4Y in 26 boys with XYY and 11 male controls and evaluated whether NLGN4Y expression correlates with anxiety, ADHD, depression and autistic behaviors (from questionnaires) in boys with XYY. The XYY cohort had increased risk of ASD behaviors on the social responsiveness scale (SRS) and increased attention deficits on the Conners' DSM-IV inattention and hyperactive scales. In contrast, there was no increase in reported symptoms of anxiety or depression by the XYY group. Peripheral expression of two Y genes in boys with XYY vs. typically developing controls was increased twofold in the XYY group. Results from the SRS total and autistic mannerisms scales, but not from the attention, anxiety or depression measures, correlated with peripheral expression of NLGN4Y in boys with XYY. Males with XYY have social phenotypes that include increased risk for autism-related behaviors and ADHD. Expression of NLGN4Y, a gene that may be involved in synaptic function, is increased in boys with XYY, and the level of expression correlates with overall social responsiveness and autism symptoms. Thus, further investigation of NLGN4Y as a plausible ASD risk gene in XYY is warranted.
© 2015 John Wiley & Sons Ltd and International Behavioural and Neural Genetics Society.

Entities:  

Keywords:  NLGN4Y; Neuroligin; XYY; social function

Mesh:

Substances:

Year:  2015        PMID: 25558953      PMCID: PMC4756915          DOI: 10.1111/gbb.12200

Source DB:  PubMed          Journal:  Genes Brain Behav        ISSN: 1601-183X            Impact factor:   3.449


  42 in total

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5.  An extra X or Y chromosome: contrasting the cognitive and motor phenotypes in childhood in boys with 47,XYY syndrome or 47,XXY Klinefelter syndrome.

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Authors:  M Geerts; J Steyaert; J P Fryns
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7.  47,XYY syndrome: clinical phenotype and timing of ascertainment.

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8.  Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disorders.

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Journal:  J Neurosci       Date:  2009-09-02       Impact factor: 6.167

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  28 in total

1.  Y chromosome gene copy number and lack of autism phenotype in a male with an isodicentric Y chromosome and absent NLGN4Y expression.

Authors:  Judith L Ross; Luke Bloy; Timothy P L Roberts; Judith Miller; Chao Xing; Lawrence A Silverman; Andrew R Zinn
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2.  Auditory evoked response delays in children with 47,XYY syndrome.

Authors:  Luke Bloy; Matthew Ku; J Christopher Edgar; Judith S Miller; Lisa Blaskey; Judith Ross; Timothy P L Roberts
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3.  Autism Spectrum Disorder in Males with Sex Chromosome Aneuploidy: XXY/Klinefelter Syndrome, XYY, and XXYY.

Authors:  Nicole R Tartaglia; Rebecca Wilson; Judith S Miller; Jessica Rafalko; Lisa Cordeiro; Shanlee Davis; David Hessl; Judith Ross
Journal:  J Dev Behav Pediatr       Date:  2017-04       Impact factor: 2.225

Review 4.  A review of neurocognitive functioning and risk for psychopathology in sex chromosome trisomy (47,XXY, 47,XXX, 47, XYY).

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Review 5.  Early neurodevelopmental and medical profile in children with sex chromosome trisomies: Background for the prospective eXtraordinarY babies study to identify early risk factors and targets for intervention.

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6.  Diagnostic efficacy and new variants in isolated and complex autism spectrum disorder using molecular karyotyping.

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Review 7.  Chromosome Y genetic variants: impact in animal models and on human disease.

Authors:  J W Prokop; C F Deschepper
Journal:  Physiol Genomics       Date:  2015-08-18       Impact factor: 3.107

8.  Behavioral phenotype in a child with Prader-Willi syndrome and comorbid 47, XYY.

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Journal:  Intractable Rare Dis Res       Date:  2016-08

9.  Microphthalmia, Linear Skin Defects, Callosal Agenesis, and Cleft Palate in a Patient with Deletion at Xp22.3p22.2.

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Journal:  J Pediatr Genet       Date:  2020-01-03

10.  Family experiences and attitudes about receiving the diagnosis of sex chromosome aneuploidy in a child.

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Journal:  Am J Med Genet C Semin Med Genet       Date:  2020-03-17       Impact factor: 3.908

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