Hosseini Sayyed-Morteza, Moulavi Fariba, Tanhaie-Vash Nima, Asgari Vajihe, Ghanaei Hamid-Reza, Abedi-Dorche Maryam, Jafarzadeh Naser, Gourabi Hossein, Shahverdi Abdol-Hossein, Dizaj Ahmad Vosough, Shirazi Abolfazl, Nasr-Esfahani Mohammad-Hossein
Department of Reproductive Biotechnology, Reproductive Biomedicine Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, Iran.
Department of Medical Physics, Tarbiat Modares University, Tehran, Iran.
PLoS One. 2016 Mar 31;11(3):e0148382. doi: 10.1371/journal.pone.0148382. eCollection 2016.
Oocyte polarity and embryonic patterning are well-established features of development in lower species. Whether a similar form of pre-patterning exists in mammals is currently under hot debate in mice. This study investigated this issue for the first time in ovine as a large mammal model. Microsurgical trisection of unfertilized MII-oocytes revealed that cortical cytoplasm around spindle (S) contained significant amounts of total maternal mRNAs and proteins compared to matched cytoplast hemispheres that were located either near (NS) or far (FS) -to-spindle. RT-qPCR provided striking examples of maternal mRNA localized to subcellular substructures S (NPM2, GMNN, H19, PCAF, DNMT3A, DNMT1, and STELLA), NS (SOX2, NANOG, POU5F1, and TET1), and FS (GCN) of MII oocyte. Immunoblotting revealed that specific maternal proteins DNMT3A and NANOG were asymmetrically enriched in MII-spindle-half of the oocytes. Topological analysis of sperm entry point (SEP) revealed that sperm preferentially entered via the MII-spindle-half of the oocytes. Even though, the topological position of first cleavage plane with regard to SEP was quite stochastic. Spatial comparison of lipid content revealed symmetrical distribution of lipids between 2-cell blastomeres. Lineage tracing using Dil, a fluorescent dye, revealed that while the progeny of leading blastomere of 2-cell embryos contributed to more cells in the developed blastocysts compared to lagging counterpart, the contributions of leading and lagging blastomeres to the embryonic-abembryonic parts of the developed blastocysts were almost unbiased. And finally, separated sister blastomeres of 2-cell embryos had an overall similar probability to arrest at any stage before the blastocyst (2-cell, 4-cell, 8-cell, and morula) or to achieve the blastocyst stage. It was concluded that the localization of maternal mRNAs and proteins at the spindle are evolutionarily conserved between mammals unfertilized ovine oocyte could be considered polar with respect to the spatial regionalization of maternal transcripts and proteins. Even though, the principal forces of this definitive oocyte polarity may not persist during embryonic cleavages.
卵母细胞极性和胚胎模式形成是低等物种发育中已确立的特征。在哺乳动物中是否存在类似形式的预模式目前在小鼠中是一个热门的争论话题。本研究首次在绵羊这一大型哺乳动物模型中探讨了这个问题。对未受精的MII期卵母细胞进行显微手术三等分显示,与位于纺锤体(S)附近(NS)或远离(FS)纺锤体的匹配细胞质半球相比,纺锤体周围的皮质细胞质含有大量的母体总mRNA和蛋白质。RT-qPCR提供了显著的例子,表明母体mRNA定位于MII期卵母细胞的亚细胞亚结构S(NPM2、GMNN、H19、PCAF、DNMT3A、DNMT1和STELLA)、NS(SOX2、NANOG、POU5F1和TET1)以及FS(GCN)。免疫印迹显示,特定的母体蛋白DNMT3A和NANOG在卵母细胞的MII期纺锤体半侧不对称富集。对精子进入点(SEP)的拓扑分析表明,精子优先通过卵母细胞的MII期纺锤体半侧进入。尽管如此,第一次卵裂平面相对于SEP的拓扑位置相当随机。脂质含量的空间比较显示2细胞期卵裂球之间脂质分布对称。使用荧光染料Dil进行谱系追踪显示,虽然与滞后的卵裂球相比,2细胞期胚胎领先卵裂球的后代在发育的囊胚中贡献了更多细胞,但领先和滞后卵裂球对发育的囊胚的胚胎-反胚胎部分的贡献几乎是无偏差的。最后,2细胞期胚胎分离的姐妹卵裂球在囊胚之前的任何阶段(2细胞期、4细胞期、8细胞期和桑葚胚期)停滞或达到囊胚期的总体概率相似。得出的结论是,母体mRNA和蛋白质在纺锤体上的定位在哺乳动物之间是进化保守的,未受精的绵羊卵母细胞在母体转录本和蛋白质的空间区域化方面可被认为是极性的。尽管如此,这种确定的卵母细胞极性的主要力量在胚胎分裂过程中可能不会持续存在。