Reade Anna, Motta-Mena Laura B, Gardner Kevin H, Stainier Didier Y, Weiner Orion D, Woo Stephanie
CVRI & Department of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, CA 94158, USA.
Structural Biology Initiative, CUNY Advanced Science Research Center, City University of New York, New York, NY 10031, USA.
Development. 2017 Jan 15;144(2):345-355. doi: 10.1242/dev.139238. Epub 2016 Dec 19.
Here, we describe an optogenetic gene expression system optimized for use in zebrafish. This system overcomes the limitations of current inducible expression systems by enabling robust spatial and temporal regulation of gene expression in living organisms. Because existing optogenetic systems show toxicity in zebrafish, we re-engineered the blue-light-activated EL222 system for minimal toxicity while exhibiting a large range of induction, fine spatial precision and rapid kinetics. We validate several strategies to spatially restrict illumination and thus gene induction with our new TAEL (TA4-EL222) system. As a functional example, we show that TAEL is able to induce ectopic endodermal cells in the presumptive ectoderm via targeted sox32 induction. We also demonstrate that TAEL can be used to resolve multiple roles of Nodal signaling at different stages of embryonic development. Finally, we show how inducible gene editing can be achieved by combining the TAEL and CRISPR/Cas9 systems. This toolkit should be a broadly useful resource for the fish community.
在此,我们描述了一种针对斑马鱼优化的光遗传学基因表达系统。该系统通过在活生物体中实现对基因表达的强大时空调控,克服了当前诱导型表达系统的局限性。由于现有的光遗传学系统在斑马鱼中显示出毒性,我们对蓝光激活的EL222系统进行了重新设计,以使其毒性最小,同时具有广泛的诱导范围、精细的空间精度和快速的动力学。我们用新的TAEL(TA4 - EL222)系统验证了几种在空间上限制光照从而限制基因诱导的策略。作为一个功能示例,我们表明TAEL能够通过靶向诱导sox32在预定外胚层中诱导异位内胚层细胞。我们还证明TAEL可用于解析胚胎发育不同阶段中Nodal信号的多种作用。最后,我们展示了如何通过结合TAEL和CRISPR/Cas9系统实现诱导型基因编辑。这个工具包应该是鱼类研究群体广泛有用的资源。