Niopek Dominik, Wehler Pierre, Roensch Julia, Eils Roland, Di Ventura Barbara
Department of Theoretical Bioinformatics, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120 Heidelberg, Germany.
Department of Bioinformatics and Functional Genomics, Synthetic Biology Group, Institute for Pharmacy and Biotechnology (IPMB), University of Heidelberg, Im Neuenheimer Feld 364, 69120 Heidelberg, Germany.
Nat Commun. 2016 Feb 8;7:10624. doi: 10.1038/ncomms10624.
Active nucleocytoplasmic transport is a key mechanism underlying protein regulation in eukaryotes. While nuclear protein import can be controlled in space and time with a portfolio of optogenetic tools, protein export has not been tackled so far. Here we present a light-inducible nuclear export system (LEXY) based on a single, genetically encoded tag, which enables precise spatiotemporal control over the export of tagged proteins. A constitutively nuclear, chromatin-anchored LEXY variant expands the method towards light inhibition of endogenous protein export by sequestering cellular CRM1 receptors. We showcase the utility of LEXY for cell biology applications by regulating a synthetic repressor as well as human p53 transcriptional activity with light. LEXY is a powerful addition to the optogenetic toolbox, allowing various novel applications in synthetic and cell biology.
主动核质运输是真核生物中蛋白质调控的关键机制。虽然可以使用一系列光遗传学工具在空间和时间上控制核蛋白的输入,但蛋白质输出问题迄今尚未得到解决。在此,我们提出了一种基于单个基因编码标签的光诱导核输出系统(LEXY),该系统能够对标记蛋白的输出进行精确的时空控制。一种组成型核内、染色质锚定的LEXY变体通过隔离细胞中的CRM1受体,将该方法扩展到对内源蛋白输出的光抑制。我们通过用光调节合成阻遏物以及人类p53转录活性,展示了LEXY在细胞生物学应用中的实用性。LEXY是光遗传学工具箱的有力补充,可在合成生物学和细胞生物学中实现各种新应用。