Yoshida M, Yagi T, Furuta Y, Takayanagi K, Kominami R, Takeda N, Tokunaga T, Chiba J, Ikawa Y, Aizawa S
Laboratory of Molecular Oncology, Tsukuba Life Science Center, RIKEN, Ibaraki, Japan.
Transgenic Res. 1995 Jul;4(4):277-87. doi: 10.1007/BF01969122.
"Gene trapping" in embryonic stem (ES) cells is a novel approach to identify a series of genes in mammals concomitant with the production of the corresponding mutant mice. However, this approach is currently unable to identify genes that are not expressed in ES cells. Here we describe a strategy to identify gene trapping clones which is not based on expression of a reporter gene. It uses the neor gene which lacks a polyadenylation signal and has a splice donor signal. Expression of the neor gene as fusion transcripts with the 3' end containing the polyadenylation signal of tagged genes allows the identification of these clones by 3' rapid amplification of the cDNA end in undifferentiated ES cells, even if the genes are not expressed in ES cells. Amplification was observed in about 25% of G418-resistant clones. Sequence analyses suggested the amplifications represent gene trapping events. The feasibility of this approach was further assessed by analysing one clone, PAT-12, in detail.
胚胎干细胞(ES细胞)中的“基因捕获”是一种在哺乳动物中鉴定一系列基因并同时产生相应突变小鼠的新方法。然而,目前这种方法无法鉴定在ES细胞中不表达的基因。在此,我们描述了一种不基于报告基因表达来鉴定基因捕获克隆的策略。它使用缺乏聚腺苷酸化信号但具有剪接供体信号的新霉素抗性基因(neor基因)。neor基因与含有标记基因聚腺苷酸化信号的3'末端融合转录本的表达,使得即使这些基因在ES细胞中不表达,也能够通过未分化ES细胞中cDNA末端的3'快速扩增来鉴定这些克隆。在约25%的G418抗性克隆中观察到了扩增。序列分析表明这些扩增代表基因捕获事件。通过详细分析一个克隆PAT - 12进一步评估了该方法的可行性。