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通过高密度SNP基因分型阵列检测到一名重度抑郁症患者存在4号染色体完全母源性单亲二体。

Complete maternal uniparental isodisomy of chromosome 4 in a subject with major depressive disorder detected by high density SNP genotyping arrays.

作者信息

Middleton Frank A, Trauzzi Marco G, Shrimpton Antony E, Gentile Karen L, Morley Christopher P, Medeiros Helena, Pato Michele T, Pato Carlos N

机构信息

Department of Neuroscience & Physiology, SUNY Upstate Medical University, Syracuse, NY, USA.

出版信息

Am J Med Genet B Neuropsychiatr Genet. 2006 Jan 5;141B(1):28-32. doi: 10.1002/ajmg.b.30250.

Abstract

Uniparental isodisomy (iUPD) is a rare genetic condition caused by non-disjunction during meiosis that ultimately leads to a duplication of either the maternal or paternal chromosome in the affected individual. Two types of disorders can result, those due to imprinted genes and those due to homozygosity of recessive disease-causing mutations. Here, we describe the third known case of complete chromosome 4 iUPD of maternal origin. This condition became apparent during whole genome linkage studies of psychiatric disorders in the Portuguese population. The proband is an adult female with normal fertility and no major medical complaints, but a history of major depressive disorder and multiple suicide attempts. The proband's siblings and parents had normal chromosome 4 genotypes and no history of mood disturbance. A brief review of other studies lends support for the possibility that genes on chromosome 4 might confer risk for mood disorders. We conclude that chromosome 4 maternal uniparental disomy (UPD) is a rare disorder that may present with a major depressive phenotype. The lack of a common disease phenotype between this and two other cases of chromosome 4 iUPD [Lindenbaum et al. [1991] Am J Med Genet 49(Suppl 285):1582; Spena et al. [2004] Eur J Hum Genet 12:891-898) would suggest that there is no vital maternal gene imprinting on chromosome 4. However, since there is no reported case of paternal chromosome 4 UPD, paternal gene imprinting on chromosome 4 cannot be excluded.

摘要

单亲二体性(iUPD)是一种罕见的遗传疾病,由减数分裂过程中的不分离引起,最终导致受影响个体中母源或父源染色体的重复。可导致两种类型的疾病,一种是由于印记基因,另一种是由于隐性致病突变的纯合性。在此,我们描述了第三例已知的母源4号染色体完全单亲二体性病例。这种情况在葡萄牙人群精神疾病的全基因组连锁研究中变得明显。先证者是一名成年女性,生育能力正常,无重大医学主诉,但有重度抑郁症病史和多次自杀未遂史。先证者的兄弟姐妹和父母4号染色体基因型正常,无情绪障碍病史。对其他研究的简要回顾支持了4号染色体上的基因可能赋予情绪障碍风险的可能性。我们得出结论,4号染色体母源单亲二体性(UPD)是一种罕见疾病,可能表现为重度抑郁表型。该病例与另外两例4号染色体iUPD病例[Lindenbaum等人[1991年]《美国医学遗传学杂志》49(增刊285):1582;Spena等人[2004年]《欧洲人类遗传学杂志》12:891 - 898]之间缺乏共同的疾病表型,这表明4号染色体上不存在至关重要的母源基因印记。然而,由于尚无父源4号染色体UPD的报道病例,因此不能排除4号染色体上的父源基因印记。

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