Department of Reproductive Biology, Reproductive Biomedicine Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, Iran.
Reproduction. 2013 Apr 15;145(4):345-55. doi: 10.1530/REP-12-0318. Print 2013 Apr.
The effect of technical steps of somatic cell nuclear transfer (SCNT) on different aspects of cloned embryo development was investigated in sheep. In vitro-matured oocytes were enucleated in the presence or absence of zona and reconstituted by three different SCNT techniques: conventional zona-intact (ZI-NT), standard zona-free (ZF-NT) and intracytoplasmic nuclear injection (ICI-NT). Stepwise alterations in nuclear remodeling events and in mRNA abundances, throughput and efficiency of cloned embryo development and cell allocation of the resulted blastocysts were assessed. Early signs of nuclear remodeling were observed as soon as 2 h post-reconstitution (hpr) for fusion-based methods of nuclear transfer (ZI-NT and ZF-NT) but were not observable until 4 hpr with the ICI-NT method. The relative mRNA abundances of HSP90AA1 (HSP90), NPM2 and ATPase genes were not affected by i) presence or absence of zona, ii) oocyte enucleation method and iii) nuclear transfer method. After reconstitution, however, the relative mRNA contents of POU5F1 (OCT4) with the ZI-NT and ZF-NT methods and of PAPOLA (PAP) with ZF-NT were significantly lower than those for the ICI-NT method. Zona removal doubled the throughput of cloned blastocyst development for the ZF-NT technique compared with ZI-NT and ICI-NT. Cleavage rate was not affected by the SCNT protocol, whereas blastocyst yield rate in ICI-NT technique (17.0±1.0%) was significantly (P<0.05; ANOVA) higher than in ZF-NT (7.1±1.5%) but not in the ZI-NT group (11.2±3.3%). Despite the similarities in total cell number, SCNT protocol changed the distribution of cells in the blastocysts, as ZF-NT-cloned blastocysts had significantly smaller inner cell mass than ZI-NT. These results indicate that technical aspects of cloning may result in the variety of cloning phenotypes.
本研究旨在探讨体细胞核移植(SCNT)技术步骤对绵羊克隆胚胎发育不同方面的影响。体外成熟卵母细胞在有无透明带的情况下去核,然后通过三种不同的 SCNT 技术进行重构:传统带透明带(ZI-NT)、标准去透明带(ZF-NT)和胞质内核注射(ICI-NT)。评估了核重构事件的逐步变化以及克隆胚胎发育的 mRNA 丰度、通量和效率,以及囊胚的细胞分配。融合法核转移(ZI-NT 和 ZF-NT)的核转移方法在重构后 2 小时(hpr)即可观察到早期核重构迹象,但 ICI-NT 方法直到 4 hpr 才可见。HSP90AA1(HSP90)、NPM2 和 ATPase 基因的相对 mRNA 丰度不受以下因素影响:i)透明带的存在与否,ii)卵母细胞去核方法和 iii)核转移方法。然而,在重构后,ZI-NT 和 ZF-NT 方法的 POU5F1(OCT4)和 ZF-NT 方法的 PAPOLA(PAP)的相对 mRNA 含量明显低于 ICI-NT 方法。与 ZI-NT 和 ICI-NT 相比,ZF-NT 技术中去除透明带使克隆囊胚发育的通量增加了一倍。SCNT 方案不影响卵裂率,而 ICI-NT 技术(17.0±1.0%)的囊胚产率显著(P<0.05;ANOVA)高于 ZF-NT(7.1±1.5%)但低于 ZI-NT 组(11.2±3.3%)。尽管总细胞数相似,但 SCNT 方案改变了囊胚中细胞的分布,因为 ZF-NT 克隆囊胚的内细胞团明显小于 ZI-NT。这些结果表明,克隆技术的各个方面可能导致克隆表型的多样性。