Rong Y S, Golic K G
Department of Biology, University of Utah, Salt Lake City, Utah 84112, USA.
Genetics. 2001 Mar;157(3):1307-12. doi: 10.1093/genetics/157.3.1307.
We previously described a method for targeted homologous recombination at the yellow gene of Drosophila melanogaster. Because only a single gene was targeted, further work was required to show whether the method could be extended to become generally useful for gene modification in Drosophila. We have now used this method to produce a knockout of the autosomal pugilist gene by homologous recombination between the endogenous locus and a 2.5-kb DNA fragment. This was accomplished solely by tracking the altered genetic linkage of an arbitrary marker gene as the targeting DNA moved from chromosome X or 2 to chromosome 3. The results indicate that this method of homologous recombination is likely to be generally useful for Drosophila gene targeting.
我们之前描述了一种在黑腹果蝇黄色基因处进行靶向同源重组的方法。由于仅靶向了单个基因,因此需要进一步开展工作以证明该方法是否能够扩展至普遍用于果蝇的基因修饰。我们现在已运用此方法,通过内源基因座与一个2.5 kb DNA片段之间的同源重组产生了常染色体拳击手基因的敲除。这完全是通过追踪一个任意标记基因的遗传连锁变化来实现的,随着靶向DNA从X染色体或2号染色体转移至3号染色体。结果表明,这种同源重组方法可能普遍适用于果蝇的基因靶向。