Miura Shoko, Miura Kiyonori, Yamamoto Toshiyuki, Yamanaka Michiko, Saito Keisuke, Hirabuki Tomoo, Kurosawa Kenji, Harada Naoki, Ishizaki-Yamasaki Yoko, Matsumoto Naomichi, Hirahara Fumiki, Yoshiura Koh-ichiro, Masuzaki Hideaki, Niikawa Norio
Department of Obstetrics and Gynecology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Am J Med Genet A. 2006 Aug 15;140(16):1737-43. doi: 10.1002/ajmg.a.31362.
Fetus-in-fetu (FIF) is a condition in which a host infant has a fetus-like mass(es) within its body. We describe here results of molecular genetic analysis in two cases of FIF. In FIF-1, a male host had two retroperitoneal fetiform masses each with a vertebral column, and in FIF-2, a fetiform mass with vertebral column was present in the cranial cavity of a male host. Genotyping of each case using microsatellite markers showed that the host infant and its fetus(es) inherited one copy each of parental alleles and shared identical genotypes. These findings were confirmed by single nucleotide polymorphism (SNP) analysis using Affymetrix GeneChip Human Mapping 50K Array, and supported a monozygotic twin theory of FIF. Analysis of the methylation status was done in both cases at the differentially methylated region (DMR) within the human IGF2-H19 locus after bisulfite treatment, methylation-specific PCR, and cloning of PCR products. Normally, only the paternal allele is methylated and the maternal allele unmethylated in DMR. However, in FIF-1, 7 (46.7%) of 15 clones from a fetiform mass and 6 (66.7%) of 9 clones from the other mass showed an unmethylated paternal allele, while the methylation status of a host infant and its fetiform mass in FIF-2 was the same in all clones examined with normal patterns. These data suggest that in FIF-1, two isolated blastocysts originated from one zygote, one of the two was implanted into (or included by) the other blastocyst during the process of methylation, and such abnormal implantation may have occurred in FIF-2 after the establishment of methylation. This is the first case of FIF showing different methylation patterns between a host infant and fetiform mass.
胎内胎(FIF)是一种宿主婴儿体内存在类似胎儿肿块的病症。我们在此描述两例胎内胎的分子遗传学分析结果。在FIF - 1中,一名男性宿主有两个腹膜后胎儿样肿块,每个肿块都有一个脊柱;在FIF - 2中,一名男性宿主的颅腔内有一个带有脊柱的胎儿样肿块。使用微卫星标记对每个病例进行基因分型表明,宿主婴儿及其胎儿各自继承了一份亲本等位基因,并且共享相同的基因型。这些发现通过使用Affymetrix GeneChip Human Mapping 50K Array进行的单核苷酸多态性(SNP)分析得到证实,并支持了胎内胎的单卵双胎理论。在亚硫酸氢盐处理、甲基化特异性PCR以及PCR产物克隆后,对两例病例的人IGF2 - H19基因座内的差异甲基化区域(DMR)进行了甲基化状态分析。正常情况下,在DMR中只有父本等位基因被甲基化,母本等位基因未被甲基化。然而,在FIF - 1中,来自一个胎儿样肿块的15个克隆中有7个(46.7%)以及来自另一个肿块的9个克隆中有6个(66.7%)显示父本等位基因未被甲基化,而在FIF - 2中,宿主婴儿及其胎儿样肿块的甲基化状态在所有检测的克隆中均为正常模式且相同。这些数据表明,在FIF - 1中,两个分离的囊胚起源于一个受精卵,其中一个在甲基化过程中植入(或被包含于)另一个囊胚,并且这种异常植入可能在FIF - 2中甲基化建立之后发生。这是首例显示宿主婴儿和胎儿样肿块之间甲基化模式不同的胎内胎病例。