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用于诱导多能干细胞生成的山羊重组Oct4蛋白的分子克隆与制备

Molecular cloning and production of caprine recombinant Oct4 protein for generation induced pluripotent stem cells.

作者信息

Singhal Dinesh K, Singhal Raxita, Malik Hruda N, Singh Surender, Kumar Sudarshan, Kaushik Jai K, Mohanty Ashok K, Malakar Dhruba

机构信息

Animal Biotechnology Centre, National Dairy Research Institute, Karnal, 132001, India.

出版信息

Mol Biol Rep. 2015 Dec;42(12):1583-91. doi: 10.1007/s11033-015-3926-2. Epub 2015 Oct 30.

DOI:10.1007/s11033-015-3926-2
PMID:26518291
Abstract

Oct4, pluripotency marker and transcription factor, expresses in embryonic stem cells. It plays a pivotal role in determination of stem cells fate. Up and down regulation of Oct4 causes differentiation of embryonic stem cells. It is one of the main transcription factors which remained concerned in every study related to induced pluripotent stem cell. Here, we report the production of goat Oct4 protein using plasmid and lentiviral based vectors. Firstly, Oct4 ORF was cloned in pAcGFP1-N1 plasmid vector and positive clones were screened with colony PCR. Oct4 was over-expressed in CHO-K1 cell line and expression was confirmed by observing green florescent protein expression in CHO-K1 cells. Secondly, Oct4 lentiviral expression construct has been prepared using pLenti-gw vector. Oct4 ORF was cloned into pLenti4/V5-DEST vector and viral particles were produced in 293FT cells. Oct4 viral particles were used to infect goat fibroblast cells. Oct4 expression was observed and confirmed in transfected goat fibroblast cells using RT-PCR. Detection of Oct4 protein in western blotting assay affirmed the capacity of over-expression of our Oct4 lentiviral vector. The lentiviral expression construct and recombinant Oct4 protein may be used for reprogramming of somatic cell into induced pluripotent stem cell.

摘要

多能性标志物及转录因子Oct4在胚胎干细胞中表达。它在干细胞命运的决定中起关键作用。Oct4的上调和下调会导致胚胎干细胞分化。它是与诱导多能干细胞相关的每项研究中一直备受关注的主要转录因子之一。在此,我们报道了使用基于质粒和慢病毒的载体生产山羊Oct4蛋白的过程。首先,将Oct4开放阅读框克隆到pAcGFP1-N1质粒载体中,并用菌落PCR筛选阳性克隆。Oct4在CHO-K1细胞系中过表达,并通过观察CHO-K1细胞中的绿色荧光蛋白表达来确认表达情况。其次,使用pLenti-gw载体制备了Oct4慢病毒表达构建体。将Oct4开放阅读框克隆到pLenti4/V5-DEST载体中,并在293FT细胞中产生病毒颗粒。Oct4病毒颗粒用于感染山羊成纤维细胞。使用RT-PCR在转染的山羊成纤维细胞中观察并确认了Oct4的表达。蛋白质印迹分析中Oct4蛋白的检测证实了我们的Oct4慢病毒载体的过表达能力。慢病毒表达构建体和重组Oct4蛋白可用于将体细胞重编程为诱导多能干细胞。

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