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Analysis of nuclear reprogramming in cloned miniature pig embryos by expression of Oct-4 and Oct-4 related genes

机译:通过Oct-4和Oct-4相关基因的表达分析克隆的小型猪胚胎中的核重编程

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摘要

Xenotransplantation is a rapidly expanding field of research and cloned miniature pigs have been considered as a model animal for it. However, the efficiency of somatic cell nuclear transfer (SCNT) is extremely low, with most clones resulting in early lethality and several kinds of aberrant development. A possible explanation for the developmental failure of SCNT embryos is insufficient reprogramming of the somatic cell nucleus by the oocyte. In order to test this, we analyzed the reprogramming capacity of differentiated fibroblast cell nuclei and embryonic germ cell nuclei with Oct-4 and Oct-4 related genes (Ndp52II, Dppa2, Dppa3, and Dppa5), which are important for embryonic development, Hand1 and GATA-4, which are important for placental development, as molecular markers using RT-PCR. The Oct-4 expression level was significantly lower (P < 0.05) in cloned hatched blastocysts derived from fibroblasts and many of fibroblast-derived clones failed to reactivate at least one of the tested genes, while most of the germ cell clones and control embryos correctly expressed these genes. In conclusion, our results suggest that the reprogramming of fibroblast-derived cloned embryos is highly aberrant and this improper reprogramming could be one reason of the early lethality and post-implantation anomalies of somatic cell-derived clones. (c) 2006 Elsevier Inc. All rights reserved.
机译:异种移植是一个快速发展的研究领域,克隆的小型猪被认为是其模型动物。但是,体细胞核转移(SCNT)的效率极低,大多数克隆会导致早期致死性和几种异常发育。 SCNT胚胎发育失败的可能解释是卵母细胞对体细胞核的重编程不足。为了测试这一点,我们分析了具有Oct-4和Oct-4相关基因(Ndp52II,Dppa2,Dppa3和Dppa5)的分化成纤维细胞核和胚胎生殖细胞核的重编程能力,这对于胚胎发育很重要,Hand1 GATA-4和GATA-4对胎盘发育很重要,它们是使用RT-PCR的分子标记。在衍生自成纤维细胞的克隆孵化胚泡中,Oct-4表达水平显着降低(P <0.05),许多成纤维细胞衍生的克隆未能重新激活至少一个测试基因,而大多数生殖细胞克隆和对照胚胎正确表达了这些基因。总之,我们的结果表明,成纤维细胞克隆的胚胎的重编程异常高,这种不正确的编程可能是体细胞衍生克隆早期致死率和植入后异常的原因之一。 (c)2006 Elsevier Inc.保留所有权利。

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