Kos Claudine H
Mineral Bioavailability Laboratory at the Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University, Boston MA, 02111, USA.
Nutr Rev. 2004 Jun;62(6 Pt 1):243-6. doi: 10.1301/nr2004.jun243-246.
Alteration of the mouse genome by conventional transgenic and gene-targeted approaches has greatly facilitated studies of gene function. However, a gene alteration expressed in the germ line may cause an embryonic lethal phenotype resulting in no viable mouse to study gene function. Similarly, a gene alteration may exert its effect in multiple different cell and tissue types, creating a complex phenotype in which it is difficult to distinguish direct function in a particular tissue from secondary effects resulting from altered gene function in other tissues. Therefore, methods have been developed to control conditions such as the timing, cell-type, and tissue specificity of gene activation or repression. This brief review provides an overview of the Cre/LoxP system for generating tissue-specific knockout mouse models.
通过传统转基因和基因靶向方法改变小鼠基因组极大地促进了基因功能的研究。然而,在生殖系中表达的基因改变可能会导致胚胎致死表型,从而没有可存活的小鼠来研究基因功能。同样,基因改变可能在多种不同的细胞和组织类型中发挥作用,产生复杂的表型,在这种表型中,很难将特定组织中的直接功能与其他组织中基因功能改变产生的间接效应区分开来。因此,已经开发出方法来控制诸如基因激活或抑制的时间、细胞类型和组织特异性等条件。本简要综述概述了用于生成组织特异性敲除小鼠模型的Cre/LoxP系统。