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Production of transgenic cloned pigs expressing the far-red fluorescent protein monomeric Plum

机译:表达远红荧光蛋白单体李子的转基因克隆猪的生产

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Monomeric Plum (Plum), a far-red fluorescent protein with photostability and photopermeability, is potentially suitable for in vivo imaging and detection of fluorescence in body tissues. The aim of this study was to generate transgenic cloned pigs exhibiting systemic expression of Plum using somatic cell nuclear transfer (SCNT) technology. Nuclear donor cells for SCNT were obtained by introducing a Plum-expression vector driven by a combination of the cytomegalovirus early enhancer and chicken beta-actin promoter into porcine fetal fibroblasts (PFFs). The cleavage and blastocyst formation rates of reconstructed SCNT embryos were 81.0% (34/42) and 78.6% (33/42), respectively. At 36–37 days of gestation, three fetuses systemically expressing Plum were obtained from one recipient to which 103 SCNT embryos were transferred (3/103, 2.9%). For generation of offspring expressing Plum, rejuvenated PFFs were established from one cloned fetus and used as nuclear donor cells. Four cloned offspring and one stillborn cloned offspring were produced from one recipient to which 117 SCNT embryos were transferred (5/117, 4.3%). All offspring exhibited high levels of Plum fluorescence in blood cells, such as lymphocytes, monocytes and granulocytes. In addition, the skin, heart, kidney, pancreas, liver and spleen also exhibited Plum expression. These observations demonstrated that transfer of the Plum gene did not interfere with the development of porcine SCNT embryos and resulted in the successful generation of transgenic cloned pigs that systemically expressed Plum. This is the first report of the generation and characterization of transgenic cloned pigs expressing the far-red fluorescent protein Plum.
机译:单体李子(Plum)是一种具有光稳定性和光渗透性的远红色荧光蛋白,可能适用于体内成像和检测人体组织中的荧光。这项研究的目的是利用体细胞核移植(SCNT)技术生成表现出Plum系统表达的转基因克隆猪。通过将由巨细胞病毒早期增强子和鸡β-肌动蛋白启动子结合驱动的Plum表达载体导入猪胎儿成纤维细胞(PFF),可获得SCNT的核供体细胞。重建的SCNT胚胎的卵裂和胚泡形成率分别为81.0%(34/42)和78.6%(33/42)。在妊娠36-37天时,从一位接受者中获得了系统表达Plum的三只胎儿,并将103个SCNT胚胎转移到了该接受者中(3/103,占2.9%)。为了产生表达李子的后代,从一个克隆的胎儿中建立了再生的PFF,并将其用作核供体细胞。由一位接受者产生了四个克隆后代和一个死产克隆后代,向其移植了117个SCNT胚胎(5 / 117,4.3%)。所有后代在血细胞(如淋巴细胞,单核细胞和粒细胞)中均表现出高水平的李子荧光。另外,皮肤,心脏,肾脏,胰腺,肝脏和脾脏也表现出李子表达。这些观察结果表明,Plum基因的转移不干扰猪SCNT胚胎的发育,并成功产生了系统表达Plum的转基因克隆猪。这是表达远红荧光蛋白Plum的转基因克隆猪的产生和表征的首次报道。

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