Schweers Brett A, Dyer Michael A
Department of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis.
Vis Neurosci. 2005 Sep-Oct;22(5):553-60. doi: 10.1017/S0952523805225026.
The use of knock-out and transgenic mice has been instrumental for advancing our understanding of retinal development and disease. In this perspective, we review existing genetic approaches to studying retinal development and present a series of new genetic tools that complement the use of standard knock-out and transgenic mice. Particular emphasis is placed on elucidating cell-autonomous and non-cell-autonomous roles of genes important for retinal development and disease in vivo. In addition, a series of gene-swapping vectors can be used to elucidate the function of proteins that regulate key processes in retinal development and a wide variety of retinopathies.
敲除小鼠和转基因小鼠的使用对推动我们对视网膜发育和疾病的理解起到了重要作用。从这个角度出发,我们回顾了现有的研究视网膜发育的遗传方法,并介绍了一系列新的遗传工具,这些工具可补充标准敲除小鼠和转基因小鼠的使用。特别强调阐明对视网膜发育和体内疾病重要的基因的细胞自主和非细胞自主作用。此外,一系列基因交换载体可用于阐明调节视网膜发育关键过程和多种视网膜病变的蛋白质的功能。