Functional characterization of NANOG in goat pre-implantation embryonic development

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
出处
期刊:Theriogenology [Elsevier]
卷期号:120: 33-39 被引量:15
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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