Skarnes W C, Moss J E, Hurtley S M, Beddington R S
Biotechnology and Biological Sciences Research Council, Centre for Genome Research, University of Edinburgh, United Kingdom.
Proc Natl Acad Sci U S A. 1995 Jul 3;92(14):6592-6. doi: 10.1073/pnas.92.14.6592.
A strategy based on the gene trap was developed to prescreen mouse embryonic stem cells for insertional mutations in genes encoding secreted and membrane-spanning proteins. The "secretory trap" relies on capturing the N-terminal signal sequence of an endogenous gene to generate an active beta-galactosidase fusion protein. Insertions were found in a cadherin gene, an unc6-related laminin (netrin) gene, the sek receptor tyrosine kinase gene, and genes encoding two receptor-linked protein-tyrosine phosphatases, LAR and PTP kappa. Analysis of homozygous mice carrying insertions in LAR and PTP kappa showed that both genes were effectively disrupted, but neither was essential for normal embryonic development.
一种基于基因诱捕的策略被开发出来,用于对小鼠胚胎干细胞进行预筛选,以寻找编码分泌蛋白和跨膜蛋白的基因中的插入突变。“分泌诱捕”依赖于捕获内源基因的N端信号序列,以产生一种活性β-半乳糖苷酶融合蛋白。在一个钙黏着蛋白基因、一个与unc6相关的层粘连蛋白(网蛋白)基因、sek受体酪氨酸激酶基因以及编码两种受体相关蛋白酪氨酸磷酸酶LAR和PTPκ的基因中发现了插入。对在LAR和PTPκ中携带插入的纯合小鼠的分析表明,这两个基因都被有效地破坏了,但对于正常胚胎发育而言,两者都不是必需的。