Thurston Alexandra, Taylor Jane, Gardner John, Sinclair Kevin D, Young Lorraine E
Wolfson Centre for Stem Cells, Tissue Engineering and Modelling, Centre for Biomolecular Sciences, University of Nottingham, University Park, Nottingham NG2 2RD, UK.
Reproduction. 2008 Jan;135(1):29-40. doi: 10.1530/REP-07-0211.
The preimplantation embryos of a range of mammals can be susceptible to disruptions in genomic imprinting mechanisms, resulting in loss of imprinting. Such disruptions can have developmental consequences involving foetal and placental growth such as Beckwith-Wiedemann syndrome in humans and large offspring syndrome in sheep. Our objective was to investigate the dynamics of establishing monoallelic expression of individual sheep imprinted genes post-fertilisation. Semi-quantitative RT-PCR was used to amplify cDNA from the sheep blastocyst, day 21 foetus and day 21 chorioallantois, to compare expression levels between biparental and parthenogenetic embryos in order to indicate allelic expression status. In common with other mammals, IGF2, PEG1 and PEG3 were paternally expressed in the day 21 conceptus, while H19, IGF2R, GRB10 and p57KIP were maternally expressed. Interestingly, GNAS was maternally expressed in the foetus, but paternally expressed in the chorioallantois at day 21. Overall, the imprinting of ovine GRB10 and IGF2R was comparable with mouse but not with human. Contrary to the trophoblast-restricted maternal expression in both mouse and human, SASH2 (sheep homologue of Mash2/HASH2) was expressed in the ovine foetus and was biallelically expressed in the chorioallantois. Differential methylation of the H19 CTCF III upstream region and IGF2R DMR2 in the chorioallantois revealed predominantly paternal and maternal methylation respectively, indicating conservation of these imprinting regulatory regions. In blastocysts, IGF2R, GRB10 and SASH2 were expressed biallelically, while the other genes were not detected. Thus, for the majority of ovine imprinted genes examined, monoallelic expression does not occur until after the blastocyst stage.
一系列哺乳动物的植入前胚胎可能易受基因组印记机制破坏的影响,从而导致印记丢失。这种破坏可能会产生涉及胎儿和胎盘生长的发育后果,如人类的贝克威思-维德曼综合征和绵羊的大后代综合征。我们的目标是研究受精后单个绵羊印记基因单等位基因表达建立的动态过程。使用半定量逆转录聚合酶链反应(RT-PCR)从绵羊囊胚、21日龄胎儿和21日龄绒膜尿囊膜中扩增互补DNA(cDNA),比较双亲胚胎和孤雌生殖胚胎之间的表达水平,以指示等位基因表达状态。与其他哺乳动物一样,胰岛素样生长因子2(IGF2)、印记基因1(PEG1)和印记基因3(PEG3)在21日龄的孕体中为父源表达,而H19、胰岛素样生长因子2受体(IGF2R)、生长因子受体结合蛋白10(GRB10)和p57KIP为母源表达。有趣的是,GNAS在胎儿中为母源表达,但在21日龄的绒膜尿囊膜中为父源表达。总体而言,绵羊GRB10和IGF2R的印记与小鼠相似,但与人类不同。与小鼠和人类中滋养层限制的母源表达相反,SASH2(Mash2/HASH2的绵羊同源物)在绵羊胎儿中表达,并且在绒膜尿囊膜中为双等位基因表达。绒膜尿囊膜中H19 CTCF III上游区域和IGF2R差异甲基化区域2(DMR2)的差异甲基化分别显示主要为父源甲基化和母源甲基化,表明这些印记调控区域具有保守性。在囊胚中,IGF2R、GRB10和SASH2为双等位基因表达,而其他基因未检测到。因此,对于大多数检测的绵羊印记基因,单等位基因表达直到囊胚阶段之后才会发生。