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不同物种着床前胚胎中Oct-4的表达模式。

Expression pattern of Oct-4 in preimplantation embryos of different species.

作者信息

Kirchhof N, Carnwath J W, Lemme E, Anastassiadis K, Schöler H, Niemann H

机构信息

Department of Biotechnology, Institute for Animal Science and Animal Behaviour (FAL), Mariensee, Neustadt, Germany.

出版信息

Biol Reprod. 2000 Dec;63(6):1698-705. doi: 10.1095/biolreprod63.6.1698.

Abstract

POU transcription factors are involved in transcriptional regulation during early embryonic development and cell differentiation. Oct-4, a member of this family, has been shown to be under strict regulation during murine development. The expression of Oct-4 correlates with the undifferentiated cell phenotype of the mouse preimplantation embryo. In this study, expression of a gene construct consisting of selected parts of the region upstream from the murine Oct-4 gene as promoter/enhancer, enhanced green fluorescent protein (EGFP) as reporter and the five exons of the murine Oct-4 gene (GOF18-delta PE EGFP) was evaluated in murine, porcine, and bovine preimplantation embryos. For comparison, expression of the endogenous Oct-4 gene was also analyzed in all three species by immunocytochemistry. The transgene construct was microinjected into zygotes cultured in vitro to various developmental stages. The EGFP fluorescence was visualized in developing embryos by excitation with blue light at different days following microinjection and showed similar expression patterns in all three species. Most embryos displayed a mosaic pattern of transgene expression. The EGFP fluorescence was not restricted to the inner cell mass (ICM) but was also seen in trophoblastic cells. An affinity-purified polyclonal antibody specific to Oct-4 was used for immunocytochemical analysis of in vivo- and in vitro-derived bovine and porcine blastocysts and also of in vivo-derived murine blastocysts. In the in vivo-derived murine embryos, Oct-4 protein was detectable in the ICM but not the trophectoderm, whereas in porcine and bovine blastocysts, derived in vivo or in vitro, Oct-4 protein was detected in both the ICM and the trophectoderm. Thus, in the two large animal species, Oct-4 expression from the endogenous gene was clearly not restricted to the pluripotent cells of the early embryo. These results show that Oct-4 regulation differs between these species and that the presence of Oct-4 protein may not be sufficient for selection of undifferentiated cell lines in domestic animals.

摘要

POU转录因子参与早期胚胎发育和细胞分化过程中的转录调控。该家族成员Oct-4在小鼠发育过程中受到严格调控。Oct-4的表达与小鼠植入前胚胎的未分化细胞表型相关。在本研究中,对一种基因构建体的表达进行了评估,该构建体由小鼠Oct-4基因上游区域的选定部分作为启动子/增强子、增强型绿色荧光蛋白(EGFP)作为报告基因以及小鼠Oct-4基因的五个外显子(GOF18-δPE EGFP)组成,评估对象为小鼠、猪和牛的植入前胚胎。为作比较,还通过免疫细胞化学分析了这三个物种中内源性Oct-4基因的表达。将转基因构建体显微注射到体外培养至不同发育阶段的受精卵中。在显微注射后的不同天数,通过蓝光激发观察发育胚胎中的EGFP荧光,结果显示在所有三个物种中其表达模式相似。大多数胚胎呈现转基因表达的嵌合模式。EGFP荧光不仅局限于内细胞团(ICM),在滋养层细胞中也可见。一种针对Oct-4的亲和纯化多克隆抗体用于对体内和体外来源的牛和猪囊胚以及体内来源的小鼠囊胚进行免疫细胞化学分析。在体内来源的小鼠胚胎中,ICM中可检测到Oct-4蛋白,但滋养外胚层中未检测到;而在体内或体外获得的猪和牛囊胚中,ICM和滋养外胚层中均检测到Oct-4蛋白。因此,在这两种大型动物物种中,内源性基因的Oct-4表达显然并不局限于早期胚胎的多能细胞。这些结果表明,这些物种之间Oct-4的调控存在差异,并且Oct-4蛋白的存在可能不足以在家畜中选择未分化细胞系。

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