Fan Lianchun, Moon Jesung, Crodian Jennifer, Collodi Paul
Department of Animal Sciences, Purdue University, 125 S. Russell Street, West Lafayette, IN 47907, USA.
Transgenic Res. 2006 Feb;15(1):21-30. doi: 10.1007/s11248-005-3225-0.
Targeted insertion of a plasmid by homologous recombination was demonstrated in zebrafish ES cell cultures. Two selection strategies were used to isolate ES cell colonies that contained targeted plasmid insertions in either the no tail or myostatin I gene. One selection strategy involved the manual isolation of targeted cell colonies that were identified by the loss of fluorescent protein gene expression. A second strategy used the diphtheria toxin A-chain gene in a positive-negative selection approach. Homologous recombination was confirmed by PCR, sequence and Southern blot analysis and colonies isolated using both selection methods were expanded and maintained for multiple passages. The results demonstrate that zebrafish ES cells have potential for use in a cell-mediated gene targeting approach.
在斑马鱼胚胎干细胞培养物中证实了通过同源重组靶向插入质粒。使用了两种选择策略来分离在无尾基因或肌肉生长抑制素I基因中含有靶向质粒插入的胚胎干细胞集落。一种选择策略涉及手动分离通过荧光蛋白基因表达缺失鉴定的靶向细胞集落。第二种策略在正负选择方法中使用白喉毒素A链基因。通过聚合酶链反应、测序和Southern印迹分析证实了同源重组,并且使用两种选择方法分离的集落被扩增并传代培养多次。结果表明斑马鱼胚胎干细胞具有用于细胞介导的基因靶向方法的潜力。