Optogenetic control of nuclear protein export

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作者
Dominik Niopek
Pierre Wehler
Julia Roensch
Roland Eils
Barbara Di Ventura
机构
[1] German Cancer Research Center (DKFZ),Department of Theoretical Bioinformatics
[2] Synthetic Biology Group,Department of Bioinformatics and Functional Genomics
[3] Institute for Pharmacy and Biotechnology (IPMB),undefined
[4] University of Heidelberg,undefined
[5] Center for Quantitative Analysis of Molecular and Cellular Biosystems (BioQuant),undefined
[6] University of Heidelberg,undefined
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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.
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