Tsukishiro Sami, Li Qing Ying, Tanemura Mitsuyo, Sugiura-Ogasawara Mayumi, Suzumori Kaoru, Sonta Shin-Ichi
Department of Obstetrics and Gynecology, Nagoya City University Medical School, Nagoya, Japan.
Department of Genetics, Institute for Developmental Research, Aichi Human Service Center, 713-8 Kamiya-cho, Kasugai, Aichi, 480-0392, Japan.
J Hum Genet. 2005;50(3):112-117. doi: 10.1007/s10038-005-0229-9. Epub 2005 Mar 4.
To investigate the involvement of uniparental disomies (UPDs) in spontaneous abortion, the polymorphic patterns of microsatellites on each chromosome were analyzed in 164 cases of abortion. Eighty-three of the 164 cases had chromosomal abnormalities. In 79 of the remaining 81 cases with normal karyotypes, the microsatellite analysis revealed that biparental patterns were present in the informative microsatellites in all chromosomes. In one of the remaining two cases, however, the polymorphic patterns of chromosome 14 appeared to be both of paternal origin. The patterns of the distal of the long arm were homozygous, and those of the remaining region were heterozygous. That is, this fetus had paternal UPD 14, originating from meiosis I nondisjunction. In the other case, the polymorphic patterns of the distal one third of the long arm of chromosome 7 were uniparental (maternal) in origin whereas those of the remaining region of this chromosome were biparental. These findings thus suggested that this chromosome might have originated from chromatid exchange between the long arms of paternal and maternal chromosome 7 at the first mitotic division. Microsatellite analysis, however, produced no evidence of duplication or deletion of any segments. The findings also suggest the possibility that some UPDs may cause spontaneous abortion.
为了研究单亲二体(UPD)在自然流产中的作用,对164例流产病例的每条染色体上微卫星的多态性模式进行了分析。164例病例中有83例存在染色体异常。在其余81例核型正常的病例中,有79例微卫星分析显示所有染色体上信息性微卫星均呈现双亲模式。然而,在其余两例中的一例中,14号染色体的多态性模式似乎均来自父方。长臂远端的模式是纯合的,其余区域的模式是杂合的。也就是说,这个胎儿存在父源单亲二体14,起源于减数分裂I不分离。在另一例中,7号染色体长臂远端三分之一的多态性模式起源于单亲(母方),而该染色体其余区域的模式是双亲的。因此,这些发现表明这条染色体可能起源于第一次有丝分裂时父方和母方7号染色体长臂之间的染色单体交换。然而,微卫星分析没有发现任何片段重复或缺失的证据。这些发现还提示某些单亲二体可能导致自然流产的可能性。