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Split-TALE: A TALE-Based Two-Component System for Synthetic Biology Applications in Planta
Author(s) -
Tom Schreiber,
Anja Prange,
T. Hoppe,
Alain Tissier
Publication year - 2019
Publication title -
plant physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.554
H-Index - 312
eISSN - 1532-2548
pISSN - 0032-0889
DOI - 10.1104/pp.18.01218
Subject(s) - effector , golden gate , synthetic biology , biology , computational biology , dna binding domain , transcription (linguistics) , dna , modular design , transcription factor , gene , genetics , dna binding protein , microbiology and biotechnology , computer science , programming language , linguistics , philosophy , civil engineering , span (engineering) , engineering
Transcription activator-like effectors (TALEs) are bacterial Type-III effector proteins from phytopathogenic Xanthomonas species that act as transcription factors in plants. The modular DNA-binding domain of TALEs can be reprogrammed to target nearly any DNA sequence. Here, we designed and optimized a two-component AND-gate system for synthetic circuits in plants based on TALEs. In this system, named split-TALE (sTALE), the TALE DNA binding domain and the transcription activation domain are separated and each fused to protein interacting domains. Physical interaction of interacting domains leads to TALE-reconstitution and can be monitored by reporter gene induction. This setup was used for optimization of the sTALE scaffolds, which result in an AND-gate system with an improved signal-to-noise ratio. We also provide a toolkit of ready-to-use vectors and single modules compatible with Golden Gate cloning and MoClo syntax. In addition to its implementation in synthetic regulatory circuits, the sTALE system allows the analysis of protein-protein interactions in planta.

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