Niida Yo, Ozaki Mamoru, Shimizu Masaki, Ueno Kazuyuki, Tanaka Tomomi
Cytogenet Genome Res. 2018;154(3):137-146. doi: 10.1159/000488572. Epub 2018 Apr 14.
Patients with autosomal recessive (AR) disorders are usually born to parents both of whom are heterozygous carriers of the disease. However, in some instances only one of the parents is a carrier and a mutation is segregated to the patient through uniparental isodisomy (UPiD). Recently, an increasing number of such case reports has been published, and it has become clear that there are several different UPiD patterns that cause AR disorders. In this article, we report 3 remarkable patients with different patterns of UPiD. We then review 85 cases collected in the literature. We realized that they can be classified into 3 patterns: UPiD of the whole chromosome, segmental UPiD with uniparental heterodisomy (UPhD), and segmental UPiD caused by post-zygotic mitotic recombination (MiRe). Whole chromosomal UPiD accounted for the majority of cases, with paternal origin accounting for approximately twice as many cases as maternal origin. Most cases of segmental UPiD with UPhD were of maternal origin, with a dominancy of nondisjunction in meiosis I, while segmental UPiD through MiRe is the smallest pattern with equal parental origin. These differences in proportion and parental origin in each pattern can be explained by considering nondisjunction during oogenesis as the starting point and UPiD as subsequent events.
常染色体隐性(AR)疾病患者的父母通常均为该疾病的杂合子携带者。然而,在某些情况下,只有一方父母是携带者,且一个突变通过单亲二体等二倍体(UPiD)传递给患者。最近,此类病例报告的数量不断增加,并且已经明确存在几种不同的导致AR疾病的UPiD模式。在本文中,我们报告了3例具有不同UPiD模式的显著病例。然后,我们回顾了文献中收集的85例病例。我们发现它们可分为3种模式:整条染色体的UPiD、伴有单亲异二体(UPhD)的节段性UPiD以及由合子后有丝分裂重组(MiRe)引起的节段性UPiD。整条染色体的UPiD占病例的大多数,父源性病例约为母源性病例的两倍。大多数伴有UPhD的节段性UPiD病例为母源性,减数分裂I期不分离占主导,而通过MiRe的节段性UPiD是最小的模式,父母源性相等。通过将卵子发生过程中的不分离作为起点,并将UPiD视为后续事件,可以解释每种模式在比例和父母源性方面的这些差异。