Yang Shang-Hsun, Agca Yuksel, Cheng Pei-Hsun, Yang Jin-Jing, Agca Cansu, Chan Anthony Wing Sang
Yerkes National Primate Research Center, Emory University, Atlanta, Georgia 30329, USA.
Genesis. 2007 Apr;45(4):177-83. doi: 10.1002/dvg.20289.
We demonstrate enhanced transgenesis in mice by intracytoplasmic injection of envelope-free lentivirus. Envelope-free lentivirus carrying the green fluorescent protein (GFP) gene under the control of the ubiquitin promoter (LVU-GFP) was microinjected into the cytoplasm of mouse zygotes prior to embryo transfer. Ninety-seven percent (31/32) of the adult mice were confirmed transgenic by PCR and Southern blot analysis; all founder mice express GFP when tail snips were examined by fluorescent microscopy prior to genomic DNA extraction. Transgene insertion numbers ranging from 1 to 32 were revealed by Southern blot analysis. Germline transmission was confirmed by the presence of transgene in F1 offspring. As expected, a lower transgenic rate (2.2%; 1/46) resulted when envelope-free LVU-GFP was microinjected into the perivitelline space (PVS) because cell recognition followed by membrane fusion between the viral envelope and the target cell is prerequisite for successful infection by envelope viruses. Here we demonstrate the competence of envelope-free lentivirus in establishing stable gene integration by germline transgenesis in mice at high efficiency, by intracytoplasmic viral injection (INVI) of envelope-free lentivirus into mouse zygotes.
我们通过将无包膜慢病毒胞质内注射到小鼠体内,证明了转基因效率的提高。将携带在泛素启动子控制下的绿色荧光蛋白(GFP)基因的无包膜慢病毒(LVU-GFP)在胚胎移植前显微注射到小鼠受精卵的细胞质中。通过PCR和Southern印迹分析,97%(31/32)的成年小鼠被确认为转基因小鼠;在提取基因组DNA之前,通过荧光显微镜检查尾尖时,所有奠基小鼠均表达GFP。Southern印迹分析显示转基因插入数为1至32个。通过F1代后代中存在转基因证实了种系传递。正如预期的那样,当将无包膜LVU-GFP显微注射到卵周隙(PVS)中时,转基因率较低(2.2%;1/46),因为包膜病毒成功感染的前提是病毒包膜与靶细胞之间的细胞识别以及随后的膜融合。在这里,我们通过将无包膜慢病毒胞质内注射(INVI)到小鼠受精卵中,证明了无包膜慢病毒通过种系转基因在小鼠中高效建立稳定基因整合的能力。