Edwards Y H, Jeremiah S J, McMillan S L, Povey S, Fisher R A, Lawler S D
Ann Hum Genet. 1984 May;48(2):119-27. doi: 10.1111/j.1469-1809.1984.tb01007.x.
The parental origin of mitochondria in hydatidiform moles has been investigated by analysis of genetic variants of mtDNA restriction enzyme patterns. In six complete moles the mtDNA was found to be maternal in origin, with no contribution from the sperm mitochondria, while the nuclear genome was shown to be exclusively paternal in five cases. The occurrence of mtDNA variation in the healthy population was investigated using white blood cells and placentae, and the most common variation occurred at the Ava II restriction sites. The variants exhibited by molar mtDNA were the same as those found in material from healthy individuals.
通过分析线粒体DNA(mtDNA)限制性酶切图谱的遗传变异,对葡萄胎中线粒体的亲本来源进行了研究。在6例完全性葡萄胎中,发现mtDNA来源于母亲,精子线粒体没有贡献,而在5例中核基因组显示完全来自父亲。使用白细胞和胎盘对健康人群中mtDNA变异的发生情况进行了研究,最常见的变异发生在Ava II限制性酶切位点。葡萄胎mtDNA表现出的变异与健康个体材料中发现的变异相同。