European Bioinformatics Institute, Genome Campus, Hinxton, Cambridgeshire CB10 1SA, UK.
Methods. 2011 Apr;53(4):411-6. doi: 10.1016/j.ymeth.2010.12.027. Epub 2010 Dec 31.
Large scale international activities for systematic conditional mouse mutagenesis, exploiting advances in the sophisticated manipulation of the mouse genome, has established the mouse as the premier organism for developing models of human disease and drug action. Conditional mutagenesis is critical for the elucidation of the gene functions that exert pleiotropic effects in a variety of cell types and tissues throughout the life of the animal. The majority of new mouse mutants are therefore designed as conditional, activated only in a specific tissue (spatial control) and/or life stage (temporal control) through biogenic Cre/loxP technologies. The full power of conditional mutant mice can therefore only be exploited with the availability of well characterized mouse lines expressing Cre-recombinase in tissue, organ and cell type-specific patterns, to allow the creation of somatic mutations in defined genes. This chapter provides an update on the current state of Cre driver mouse lines worldwide, and reviews the available public databases and portals that capture critical details of Cre driver lines such as the efficiency of recombination, cell tissue specificity, or genetic background effects. The continuously changing landscape of these mouse resources reflects the rapid progression of research and development in conditional and inducible mouse mutagenesis.
大规模的国际系统条件性小鼠诱变活动,利用了对小鼠基因组的复杂操作的进展,确立了小鼠作为开发人类疾病和药物作用模型的首选生物。条件性诱变对于阐明在动物的整个生命过程中在各种细胞类型和组织中发挥多效性的基因功能至关重要。因此,大多数新的小鼠突变体都是通过生物生成的 Cre/loxP 技术设计为条件性的,仅在特定组织(空间控制)和/或生命阶段(时间控制)中激活。只有在具有表达 Cre 重组酶的特征明确的小鼠系的情况下,才能充分利用条件性突变小鼠的全部潜力,这些小鼠系在组织、器官和细胞类型特异性模式中表达 Cre 重组酶,以允许在定义的基因中创建体细胞突变。本章提供了全球 Cre 驱动小鼠系的最新状态更新,并回顾了可用的公共数据库和门户,这些数据库和门户捕获了 Cre 驱动系的关键细节,例如重组效率、细胞组织特异性或遗传背景效应。这些小鼠资源的不断变化的格局反映了条件性和诱导性小鼠诱变研究和开发的快速进展。