同源盒蛋白纳米
雷克斯1
SOX2
内细胞团
胚泡
基因敲除
胚胎干细胞
纳米同源盒蛋白
生物
分子生物学
胚胎
诱导多能干细胞
细胞生物学
胚胎发生
男科
基因
遗传学
医学
作者
Razieh Habibi,Sayyed Morteza Hosseini,Faezeh Ghazvini Zadegan,Mehdi Hajian,S. Ostadhosseini,Nima Tanhaei Vash,Azadeh Naddafpour,Mohammad Hossein Nasr-Esfahani
标识
DOI:10.1016/j.theriogenology.2018.07.023
摘要
Nanog as a novel pluripotent cell-specific gene plays important roles in regulation of signaling pathways for maintenance and induction of pluripotency in inner cell mass (ICM) and embryonic stem cells (ESC) in mouse. The molecular features and transcription regulation of NANOG gene in domestic animals are not well defined. In this study, we performed knockdown of NANOG mRNA in goat embryos and examined its effect on early embryonic development. Presumptive zygotes were injected with a volume of 8-10 pl NANOG or scrambled (SCR) siRNA, and subsequently cleavage and blastocyst formation rate were assessed. Furthermore, gene expression analysis was carried out in 6-8 cell and blastocyst derived embryos from non-injected controls, SCR - and siRNA-injected presumptive zygotes. Cleavage and blastocyst rates in siRNA groups were insignificantly lower than the control and SCR groups. Embryos with reduced expression of NANOG showed decrease in number of trophectoderm (TE) and total cells in blastocysts. Analysis of expression of developmentally important genes (SOX2, OCT4 and NANOG), which work as a network, showed that NANOG knockdown results in significant increase in expression of SOX2 and OCT4 and among the possible target genes (CDX2, REX1 and GATA4) of this network, only GATA4 showed increased expression. Our results suggest that NANOG is likely to be required for proliferation of trophoblastic cells.
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