The Fels Institute for Cancer Research and Molecular Biology, Temple University School of Medicine, Philadelphia, PA 19140, USA.
Hum Reprod. 2009 Nov;24(11):2718-28. doi: 10.1093/humrep/dep286. Epub 2009 Aug 6.
The ooplasm plays a central role in forming the paternal pronucleus, and subsequently in regulating the expression of paternally inherited chromosomes. Previous studies in mice have revealed genetic differences in paternal genome processing by ooplasm of different genotypes. Ooplasm donation coupled to intracytoplasmic sperm injection (ICSI) has been used in human assisted reproductive technology (ART). This procedure exposes the developing paternal pronucleus to 'foreign' ooplasm, which may direct aberrant epigenetic processing. The potential effects of the foreign ooplasm on epigenetic information in the paternal pronucleus are unknown; however, some human progeny from ooplasm donation procedures display abnormalities.
In this study, we employed inter-genotype ooplasm transfer followed by ICSI using two mouse strains, C57BL/6 and DBA/2, to explore the influence of foreign ooplasm on paternal pronucleus function. In order to assay for effects on the paternal genome without masking effects of the maternal genome, we examined ooplasm effects in diploid androgenones, which are produced by pronuclear transfer to contain exclusively two paternal sets of chromosomes, in combination with ICSI.
There was no significant effect of intra-strain ooplasm transfer among androgenones made with either C57BL/6 or DBA/2 oocytes. There was a significant negative effect on androgenone blastocyst development with inter-genotype transfer (10% volume) of DBA/2 ooplasm to C57BL/6 oocytes (P < 0.05). The reciprocal inter-genotype ooplasm transfer had no significant effect.
Thus, inter-genotype ooplasm transfer in conjunction with ICSI can alter the function of the paternal genome. However, the effect of foreign ooplasm is restricted to a negative effect, with no evidence of a positive effect. This study provides important new information about the possible consequences of ooplasm donation in human ART.
卵质在形成父本原核并随后调节父本遗传染色体的表达方面起着核心作用。先前在小鼠中的研究揭示了不同基因型的卵质对父本基因组处理的遗传差异。卵质捐赠与胞质内精子注射(ICSI)已在人类辅助生殖技术(ART)中使用。该程序使发育中的父本原核暴露于“外来”卵质中,这可能导致异常的表观遗传处理。关于“外来”卵质对父本原核中表观遗传信息的潜在影响尚不清楚;然而,一些来自卵质捐赠程序的人类后代表现出异常。
在这项研究中,我们采用了两种小鼠品系(C57BL/6 和 DBA/2)的基因型间卵质转移,然后进行 ICSI,以探索“外来”卵质对父本原核功能的影响。为了在不掩盖母本基因组影响的情况下检测父本基因组的影响,我们在二倍体雄激素原核中检测了卵质的影响,雄激素原核是通过原核转移产生的,仅包含两套父本染色体,与 ICSI 结合使用。
在 C57BL/6 或 DBA/2 卵母细胞中进行的同一种卵质转移对雄激素原核没有显著影响。用 DBA/2 卵质(10%体积)进行基因型间转移对 C57BL/6 卵母细胞的雄激素原核胚胎发育有显著的负面影响(P < 0.05)。相反的基因型间卵质转移没有显著影响。
因此,与 ICSI 结合的基因型间卵质转移可以改变父本基因组的功能。然而,“外来”卵质的影响仅限于负向影响,没有正向影响的证据。这项研究为人类 ART 中卵质捐赠的可能后果提供了重要的新信息。