Jasin M, Berg P
Department of Biochemistry, Stanford University Medical Center, California 94305.
Genes Dev. 1988 Nov;2(11):1353-63. doi: 10.1101/gad.2.11.1353.
Homologous integrations into a nonselectable target locus have been highly enriched for following DNA transfections into mammalian cells. The target gene, the SV40 early region in COS1 cells, provides transcription signals to activate a defective selectable marker, the gpt gene. We find that nearly half of the selected clones have integrated the gpt gene at the homologous sequence in the COS1 genome. This is an estimated 100-fold enrichment for homologous events compared with transfections in which the gpt gene is transcriptionally active. As shown for yeast integration events, a double-strand break at a position of homology between the transfected DNA and the genomic target is necessary to achieve a high frequency of homologous integrations. Furthermore, the arrangement of sequences at the integration site includes a repair of the double-strand gap, which was present on the transfected DNA, suggesting that similarities exist between yeast and mammalian integrations. The experimental design, in which a defective marker is activated following a homologous integration, may have general applications for gene targeting in mammalian cells.
在将DNA转染到哺乳动物细胞后,同源整合到非选择性靶位点的情况得到了高度富集。靶基因,即COS1细胞中的SV40早期区域,提供转录信号以激活缺陷型选择标记基因gpt。我们发现,近一半的选定克隆在COS1基因组的同源序列处整合了gpt基因。与gpt基因转录活跃的转染相比,这是同源事件的约100倍富集。正如酵母整合事件所示,转染DNA与基因组靶标之间同源位置的双链断裂对于实现高频率的同源整合是必要的。此外,整合位点的序列排列包括对转染DNA上存在的双链缺口的修复,这表明酵母和哺乳动物的整合之间存在相似性。在同源整合后激活缺陷型标记的实验设计可能在哺乳动物细胞的基因靶向中具有广泛应用。