Cre/loxP system for generating tissue-specific knockout mouse models
被引:91
作者:
Kos, CH
论文数: 0引用数: 0
h-index: 0
机构:
Tufts Univ, USDA, Human Nutr Res Ctr Aging, Mineral Bioavailabil Lab, Boston, MA 02111 USATufts Univ, USDA, Human Nutr Res Ctr Aging, Mineral Bioavailabil Lab, Boston, MA 02111 USA
Kos, CH
[1
]
机构:
[1] Tufts Univ, USDA, Human Nutr Res Ctr Aging, Mineral Bioavailabil Lab, Boston, MA 02111 USA
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.