生物
斑马鱼
病毒载体
体细胞
病毒学
载体(分子生物学)
绿色荧光蛋白
基因
生殖系
细胞培养
细胞生物学
报告基因
胚胎
分子生物学
遗传学
基因表达
重组DNA
作者
Toshihiro Kawasaki,Kenji Saito,Kaoru Mitsui,Masahito Ikawa,Masakane Yamashita,Yoshihito Taniguchi,Shunichi Takeda,Kohnosuke Mitani,Noriyoshi Sakai
出处
期刊:Zebrafish
[Mary Ann Liebert, Inc.]
日期:2009-08-30
卷期号:6 (3): 253-258
被引量:21
标识
DOI:10.1089/zeb.2009.0596
摘要
Viral vectors represent a tractable system that can efficiently introduce an exogenous gene into different target cells and are thus a potentially powerful genetic manipulation tool. In our current study, we investigated the infection efficiency of mammalian virus vectors, adenoviruses (Ads), adeno-associated viruses, and lentiviruses to the Sertoli cell line and the newly established cell line from a single embryo in zebrafish. Among the viral vectors tested, Ads showed the highest infection efficiency of 107–108 green fluorescent protein–transducing units (gtu)/mL in zebrafish cells. In addition, the adenoviral vector was also infected at 105 gtu/mL in the medaka testicular somatic cell line that was established from the testes of p53-deficient mutant. Further, we found that Ads could successfully infect cultured male zebrafish germ cells. Our results thus indicate that the adenoviral vector could be used as a chromosomally nonintegrating vector system in zebrafish.
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