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Turner syndrome and the evolution of human sexual dimorphism.特纳综合征与人类性二态性的进化
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Sex-specific parent-of-origin allelic expression in the mouse brain.雌雄异体的亲本等位基因在小鼠大脑中的表达。
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High-resolution analysis of parent-of-origin allelic expression in the mouse brain.高分辨率分析小鼠大脑中亲本来源等位基因的表达。
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Random X inactivation and extensive mosaicism in human placenta revealed by analysis of allele-specific gene expression along the X chromosome.随机 X 染色体失活和广泛嵌合体在人类胎盘组织中的鉴定:X 染色体基因表达的等位基因特异性分析。
PLoS One. 2010 Jun 4;5(6):e10947. doi: 10.1371/journal.pone.0010947.
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Novel genetic aspects of Klinefelter's syndrome.克氏综合征的新遗传学方面。
Mol Hum Reprod. 2010 Jun;16(6):386-95. doi: 10.1093/molehr/gaq019. Epub 2010 Mar 12.
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Sex differences in molecular neuroscience: from fruit flies to humans.性别在分子神经科学中的差异:从果蝇到人。
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The cognitive phenotype in Klinefelter syndrome: a review of the literature including genetic and hormonal factors.克兰费尔特综合征的认知表型:包括遗传和激素因素在内的文献综述。
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[Confirmatory factor analysis of schizotypal personality traits in university students].[大学生分裂型人格特质的验证性因素分析]
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额外 X 染色体的亲本来源可能会对克莱恩费尔特综合征的精神病理学产生不同的影响。

The parent-of-origin of the extra X chromosome may differentially affect psychopathology in Klinefelter syndrome.

机构信息

Department of Psychiatry, Rudolf Magnus Institute of Neuroscience, University Medical Center, Utrecht, the Netherlands.

出版信息

Biol Psychiatry. 2010 Dec 15;68(12):1156-62. doi: 10.1016/j.biopsych.2010.08.034. Epub 2010 Oct 29.

DOI:10.1016/j.biopsych.2010.08.034
PMID:21035791
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3038433/
Abstract

BACKGROUND

Several genetic mechanisms have been proposed for the variability of the Klinefelter syndrome (KS) phenotype such as the parent-of-origin of the extra X chromosome. Parent-of-origin effects on behavior in KS can possibly provide insights into X-linked imprinting effects on psychopathology that may be extrapolated to other populations. Here, we investigated whether the parent-of-origin of the supernumerary X chromosome influences autistic and schizotypal symptom profiles in KS.

METHODS

Parent-of-origin of the X chromosome was determined through analysis of the polymorphic CAG tandem repeat of the androgen receptor gene. Autistic traits (Autism Diagnostic Interview-Revised) were measured in a younger KS sample (n = 33) with KS and schizotypal traits (Schizotypal Personality Questionnaire) were assessed in an older KS sample (n = 43). Scale scores on these questionnaires were entered in statistical analyses to test parent-of-origin effects.

RESULTS

The results show that parent-of-origin of the X chromosome is reflected in autistic and schizotypal symptomatology. Differences were shown in the degree of both schizotypal and autistic symptoms between the parent-of-origin groups. Furthermore, the parent-of-origin could be correctly discriminated in more than 90% of subjects through Autism Diagnostic Interview-Revised scales and in around 80% of subjects through Schizotypal Personality Questionnaire scales.

CONCLUSIONS

These findings point to parent-of-origin effects on psychopathology in KS and indicate that imprinted X chromosomal genes may have differential effects on autistic and schizotypal traits. Further exploration of imprinting effects on psychopathology in KS is needed to confirm and expand on our findings.

摘要

背景

已经提出了几种遗传机制来解释克氏综合征(KS)表型的变异性,例如额外 X 染色体的亲本来源。KS 中行为的亲本来源效应可能为 X 连锁印迹对精神病理学的影响提供见解,这些影响可能会推广到其他人群。在这里,我们研究了额外 X 染色体的亲本来源是否会影响 KS 中的自闭症和精神分裂症样症状特征。

方法

通过雄激素受体基因的多态性 CAG 串联重复分析来确定 X 染色体的亲本来源。在年轻的 KS 样本(n = 33)中测量自闭症特征(自闭症诊断访谈修订版),在较年长的 KS 样本(n = 43)中评估精神分裂症样特征(精神分裂症人格问卷)。将这些问卷的量表评分输入统计分析中,以测试亲本来源效应。

结果

结果表明,X 染色体的亲本来源反映在自闭症和精神分裂症样症状中。在亲本来源组之间,精神分裂症样和自闭症症状的严重程度都存在差异。此外,通过自闭症诊断访谈修订版量表,可正确区分 90%以上的受试者的亲本来源,通过精神分裂症人格问卷量表,可正确区分约 80%的受试者的亲本来源。

结论

这些发现指向 KS 中精神病理学的亲本来源效应,并表明印迹 X 染色体基因可能对自闭症和精神分裂症样特征有不同的影响。需要进一步探索 KS 中印迹对精神病理学的影响,以证实和扩展我们的发现。