Melton D W
Institute of Cell and Molecular Biology, Edinburgh University, Scotland.
Bioessays. 1994 Sep;16(9):633-8. doi: 10.1002/bies.950160907.
Mice with alterations to specific endogenous genes can be produced by gene targeting in embryonic stem cells. The field has developed rapidly over the past decade, so that large numbers of mice with different gene deficiencies have been generated. Knockout mice provide an ideal opportunity to analyse the function of individual mammalian genes and to model a range of human inherited disorders. This powerful approach has also identified numerous examples of gene redundancy and has highlighted the need to consider metabolic differences between man and mouse in disease modelling. More sophisticated gene-targeting methods are now being used to introduce subtle gene alterations. In the future, more refined genetic analysis and genome, rather than individual gene, alterations will be achieved by incorporating site-specific recombination into targeting strategies. Gene targeting could also make a contribution to improved protocols for gene therapy.
通过对胚胎干细胞进行基因打靶,可以培育出特定内源基因发生改变的小鼠。在过去十年中,该领域发展迅速,已培育出大量具有不同基因缺陷的小鼠。基因敲除小鼠为分析单个哺乳动物基因的功能以及模拟一系列人类遗传疾病提供了理想的机会。这种强大的方法还发现了许多基因冗余的例子,并突出了在疾病建模中考虑人类和小鼠代谢差异的必要性。现在正在使用更复杂的基因打靶方法来引入细微的基因改变。未来,通过将位点特异性重组纳入打靶策略,将实现更精细的遗传分析和基因组而非单个基因的改变。基因打靶也可能有助于改进基因治疗方案。