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9p缺失综合征中从头发生的9号染色体缺失的亲本来源。

Parental origin of De Novo chromosome 9 deletions in del(9p) syndrome.

作者信息

Micale M A, Haren J M, Conroy J M, Crowe C A, Schwartz S

机构信息

Department of Genetics and Center for Human Genetics, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.

出版信息

Am J Med Genet. 1995 May 22;57(1):79-81. doi: 10.1002/ajmg.1320570118.

Abstract

Parental origin of de novo deletions in the short arm of chromosome 9 in patients with a clinical diagnosis of del(9p) syndrome was assessed in 13 patients using polymerase chain reaction (PCR) analysis of highly polymorphic dinucleotide repeat microsatellite markers located in the putative deleted region. The deletion was found to be of paternal origin in 9 cases and of maternal origin in the remaining 4 cases, suggesting that the molecular event resulting in the deletion occurs in both male and female gametogenesis and that genomic imprinting does not appear to play a role in the pathogenesis of del(9p) syndrome.

摘要

利用位于假定缺失区域的高度多态性二核苷酸重复微卫星标记进行聚合酶链反应(PCR)分析,对13例临床诊断为9p缺失综合征患者9号染色体短臂的新生缺失的亲本来源进行了评估。发现9例缺失源自父方,其余4例源自母方,这表明导致缺失的分子事件在雄性和雌性配子发生过程中均会发生,且基因组印记似乎在9p缺失综合征的发病机制中不起作用。

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