泛嗜性逆转录病毒载体的整合、表达和种在水稻中的种系传播。

J K Lu, J C Burns, T T Chen
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引用次数: 0

摘要

利用泛嗜性逆转录病毒载体将转基因引入日本稻(Oryzias latipes)。这些载体包含Moloney小鼠白血病病毒(Mo-MLV)的长末端重复序列(LTR)和劳斯肉瘤病毒(RSV) LTR序列调控的报告基因(neo或lacZ)。由于这些伪型逆转录病毒载体含有水泡性口炎病毒包膜糖蛋白(VSV-G),它们具有非常广泛的宿主细胞范围,可以感染许多哺乳动物物种。在4 × 10(4) cfu的嗜性逆转录病毒载体存在下,在不同的电压设置下电穿孔新受精的medaka卵(完整的或去角质的)。随着电穿孔幅度的增大,泛性逆转录病毒载体处理的胚胎存活率在65% ~ 20%之间。脱毛对胚胎存活率没有显著影响。PCR扩增显示,2个月大的鱼中有多达60%的原病毒序列。脱去棉皮可以提高基因转移的效率。此外,用无电穿孔的泛性逆转录病毒载体对去角质胚胎进行过夜孵育,也导致60%的胚胎在不影响存活率的情况下实现原体整合。从聚合酶链反应(PCR)中分离的DNA样本作为阳性F1反应动物的Southern blot分析证实了原病毒的单个拷贝整合到宿主基因组中。在与野生型雄鱼的回交中,3只P1转基因雌鱼将原病毒序列传给了50%的F1后代,这表明这些P1鱼的整个种系都被泛嗜性逆转录病毒载体转化了。利用反转录(RT)-PCR扩增neo mRNA序列,检测F1转基因个体中新霉素磷酸转移酶基因的表达情况。此外,在4日龄F1转基因个体中也观察到β -半乳糖苷酶转基因的表达。因此,泛嗜性逆转录病毒载体提供了一种稳定导入和表达外源基因的简便方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pantropic retroviral vector integration, expression, and germline transmission in medaka (Oryzias latipes).

Pantropic retroviral vectors were used to introduce transgenes into Japanese medaka (Oryzias latipes). These vectors contain the long terminal repeat (LTR) sequence of Moloney murine leukemia virus (Mo-MLV) and a reporter gene (neo or lacZ) regulated by the LTR sequence of rous sarcoma virus (RSV). Because these pseudotyped retroviral vectors contain the vesicular stomatitis virus envelope glycoprotein (VSV-G), they have an extremely broad host cell range and can infect many no mammalian species. Newly fertilized medaka eggs (intact or dechorionated) were electroporated at different voltage settings in the presence of 4 x 10(4) cfu of pantropic retroviral vector. The survival rates of the pantropic retroviral vector-treated embryos ranged from 65% to 20% with increasing amplitude of electroporation. Dechorionation did not substantially affect the survival rate of embryos. PCR amplification demonstrated proviral sequences in up to 60% of the 2-month-old fish. The efficiency of gene transfer was enhanced by dechorionation. Furthermore, overnight incubation of dechorionated embryos with pantropic retroviral vectors without electroporation also resulted in proviral integration in 60% of the embryos without compromising survival rate. Southern blot analysis of DNA samples isolated from polymerase chain reaction (PCR) as positive F1 reaction animals confirmed the integration of a single copy of the provirus into the host genome. Three P1 transgenic females transmitted the proviral sequence to 50% of their F1 progeny in a back cross with wild-type males, suggesting that the entire germline of these P1 fish was transformed by the pantropic retroviral vector. Expression of the neomycin phosphotranferase transgene in F1 transgenic individuals was detected by reverse transcription (RT)-PCR amplification of the neo mRNA sequence. Furthermore, expression of a beta-galactosidase transgene was also observed in 4-day-old F1 transgenic individuals. Thus, pantropic retroviral vectors provide a convenient method to stably introduce and express foreign genes in medaka.

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