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Scientists can inactivate or knock out a gene in animals, commonly mice, to learn more about the function of the gene, usually by replacing it with a targeting vector, an engineered piece of DNA.
The targeting vector has sequences that are homologous, identical to the sequences before and after the gene. It usually also has a positive selection marker such as the gene for neomycin resistance NeoR in the middle and a negative selection marker like the gene for thymidine kinase TK at one end.
When introduced into embryonic stem cells it replaces the gene through homologous recombination which occurs naturally between stretches of DNA with similar sequences. Cells where the gene has been correctly replaced will contain the positive marker but not the negative one allowing them to be identified in culture. These cells are then inserted into a mouse embryo and implanted into the uterus of a female. The resulting mouse has a combination of normal cells and cells with the gene knocked out on one chromosome.
These mice are then bred to generate so-called knockout mice that are homozygous for the knockout in all cells.
为了进一步了解基因的功能,研究人员可以通过创造基因工程敲除动物来观察基因失活或“敲除”后的情况。敲除小鼠作为人类疾病(如癌症、帕金森病和糖尿病)的模型特别有用。
基因可以随机剔除,也可以针对特定的基因。为了敲除一个特定的基因,一个被称为靶向载体的工程DNA片段被用来代替正常基因,从而使其失活。
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