Division of Neurobiology and Bioinformatics, National Institute for Physiological Sciences, Okazaki Aichi, Japan.
Biol Psychiatry. 2010 Apr 15;67(8):770-3. doi: 10.1016/j.biopsych.2009.12.020. Epub 2010 Feb 16.
We created the Flexible Accelerated STOP Tetracycline Operator (tetO)-knockin (FAST) system, an efficient method for manipulating gene expression in vivo to rapidly screen animal models of disease. A single gene targeting event yields two distinct knockin mice-STOP-tetO and tetO knockin-that permit generation of multiple strains with variable expression patterns: 1) knockout, 2) Cre-mediated rescue, 3) tetracycline-controlled transcriptional activator (tTA)-mediated misexpression, 4) tetracycline-controlled transcriptional activator (tTA)-mediated overexpression, and 5) tetracycline-controlled transcriptional silencer (tTS)-mediated conditional knockout/knockdown. Using the FAST system, multiple gain-of-function and loss-of-function strains can therefore be generated on a time scale not previously achievable. These strains can then be screened for clinically relevant abnormalities. We demonstrate the flexibility and broad applicability of the FAST system by targeting several genes encoding proteins implicated in neuropsychiatric disorders: Mlc1, neuroligin 3, the serotonin 1A receptor, and the serotonin 1B receptor.
我们创建了灵活加速四环素操纵子(tetO)敲入(FAST)系统,这是一种在体内操纵基因表达的有效方法,可用于快速筛选疾病动物模型。单次基因靶向事件产生两种不同的敲入小鼠 - STOP-tetO 和 tetO 敲入 - 允许生成具有不同表达模式的多种菌株:1)敲除,2)Cre 介导的拯救,3)四环素调控转录激活剂(tTA)介导的异位表达,4)四环素调控转录激活剂(tTA)介导的过表达,以及 5)四环素调控转录沉默剂(tTS)介导的条件性敲除/敲低。使用 FAST 系统,因此可以在以前无法实现的时间尺度上生成多种功能获得和功能丧失菌株。然后可以筛选这些菌株是否存在与临床相关的异常。我们通过靶向几个编码与神经精神疾病相关蛋白的基因来证明 FAST 系统的灵活性和广泛适用性:Mlc1、neuroligin 3、5-羟色胺 1A 受体和 5-羟色胺 1B 受体。