Centre de recherche en reproduction, développement et santé intergénérationnelle, Département des Sciences Animales, Faculté des sciences de l'agriculture et de l'alimentation, Université Laval, Québec, Québec, Canada.
Mol Reprod Dev. 2022 Jul;89(7):290-297. doi: 10.1002/mrd.23621. Epub 2022 Jun 13.
Imprinted genes are inherited with different DNA methylation patterns depending on the maternal or paternal origin of the allele. In cattle (Bos taurus), abnormal methylation of these genes is linked to the large offspring syndrome, a neonatal overgrowth phenotype analogous to the human Beckwith-Wiedemann syndrome. We hypothesized that in bovine oocytes, some of the methylation patterns on maternally imprinted genes are acquired in the last phase of folliculogenesis. The pyrosequencing analysis of IGF2R, KCNQ1, PLAGL1, and SNRPN imprinted genes showed no clear progression of methylation in oocytes from follicles 1-2 mm (late pre antral/early antral) and up. Instead, these oocytes displayed complete methylation at the imprinted differentially methylated regions (>80%). Other mechanisms related to imprint maintenance should be investigated to explain the hypomethylation at IGF2R, KCNQ1, PLAGL1, and SNRPN maternally imprinted sites observed in some bovine embryos.
印迹基因的遗传与等位基因的母源或父源有关,其 DNA 甲基化模式不同。在牛(Bos taurus)中,这些基因的异常甲基化与大胎综合征有关,这是一种类似于人类 Beckwith-Wiedemann 综合征的新生儿过度生长表型。我们假设在牛卵母细胞中,一些母系印迹基因的甲基化模式是在卵泡发生的最后阶段获得的。IGF2R、KCNQ1、PLAGL1 和 SNRPN 印迹基因的焦磷酸测序分析显示,1-2 毫米(晚期前腔卵泡/早期腔卵泡)和以上卵泡中的卵母细胞的甲基化没有明显进展。相反,这些卵母细胞在印迹差异甲基化区域(>80%)显示出完全甲基化。应该研究其他与印迹维持相关的机制,以解释在一些牛胚胎中观察到的 IGF2R、KCNQ1、PLAGL1 和 SNRPN 母系印迹位点的低甲基化。