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新发罗伯逊易位形成的亲本来源及时间

Parental origin and timing of de novo Robertsonian translocation formation.

作者信息

Bandyopadhyay Ruma, Heller Anita, Knox-DuBois Cami, McCaskill Christopher, Berend Sue Ann, Page Scott L, Shaffer Lisa G

机构信息

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.

出版信息

Am J Hum Genet. 2002 Dec;71(6):1456-62. doi: 10.1086/344662. Epub 2002 Nov 6.

Abstract

Robertsonian translocations (ROBs) are the most common chromosomal rearrangements in humans. ROBs are whole-arm rearrangements between the acrocentric chromosomes 13-15, 21, and 22. ROBs can be classified into two groups depending on their frequency of occurrence, common (rob(13q14q) and rob(14q21q)), and rare (all remaining possible nonhomologous combinations). Herein, we have studied 29 case subjects of common and rare de novo ROBs to determine their parental origins and timing of formation. We compared these case subjects to 35 published case subjects of common ROBs and found that most common ROBs apparently have the same breakpoints and arise mainly during oogenesis (50/54). These probably form through a common mechanism and have been termed "class 1." Collectively, rare ROBs also occur mostly during oogenesis (7/10) but probably arise through a more "random" mechanism or a variety of mechanisms and have been termed "class 2." Thus, we demonstrate that although both classes of ROBs occur predominantly during meiosis, the common, class 1 ROBs occur primarily during oogenesis and likely form through a mechanism distinct from that forming class 2 ROBs.

摘要

罗伯逊易位(ROBs)是人类中最常见的染色体重排。罗伯逊易位是13 - 15号、21号和22号近端着丝粒染色体之间的全臂重排。根据其发生频率,罗伯逊易位可分为两组,常见的(rob(13q14q)和rob(14q21q))以及罕见的(所有其余可能的非同源组合)。在此,我们研究了29例常见和罕见的新发罗伯逊易位病例,以确定其亲本来源和形成时间。我们将这些病例与35例已发表的常见罗伯逊易位病例进行比较,发现大多数常见的罗伯逊易位显然具有相同的断点,并且主要在卵子发生过程中出现(50/54)。这些可能通过一种共同机制形成,被称为“1类”。总体而言,罕见的罗伯逊易位也大多在卵子发生过程中出现(7/10),但可能通过更“随机”的机制或多种机制产生,被称为“2类”。因此,我们证明,尽管这两类罗伯逊易位都主要在减数分裂过程中发生,但常见的1类罗伯逊易位主要在卵子发生过程中出现,并且可能通过一种与形成2类罗伯逊易位不同的机制形成。

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