Byrne G W, Ruddle F H
Department of Biology, Yale University, New Haven, CT 06511.
Proc Natl Acad Sci U S A. 1989 Jul;86(14):5473-7. doi: 10.1073/pnas.86.14.5473.
Transgenic mice have been used to study gene function and regulation by introducing inducible or tissue-specific transgenes. This approach is generally limited to studying gene function in adult mice since ectopic expression of many interesting genes is disease causing or may be lethal to the developing embryo. To extend the utility of the transgenic mouse system to the early stages of embryogenesis, we have developed a two-tiered method of gene regulation to control transgene expression. Our multiplex gene regulatory system (MGR) allows the establishment of transgenic lines that harbor inducible potentially lethal transgenes. These inducible transgenes are activated only when mated to a second transgenic animal. Induction in the MGR system provides a high degree of temporal and spatial control over transgene expression and should be suitable for engineering "gain of function mutations" for many developmental genes.
转基因小鼠已被用于通过引入可诱导或组织特异性转基因来研究基因功能和调控。这种方法通常仅限于研究成年小鼠中的基因功能,因为许多有趣基因的异位表达会导致疾病或可能对发育中的胚胎致死。为了将转基因小鼠系统的效用扩展到胚胎发生的早期阶段,我们开发了一种两级基因调控方法来控制转基因表达。我们的多重基因调控系统(MGR)允许建立携带可诱导的潜在致死转基因的转基因品系。这些可诱导的转基因仅在与第二只转基因动物交配时才被激活。MGR系统中的诱导对转基因表达提供了高度的时间和空间控制,并且应该适用于为许多发育基因设计“功能获得突变”。