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Chapitre D'ouvrage Année : 2016

Fast and Efficient Cloning of Cis-Regulatory Sequences for High-Throughput Yeast One-Hybrid Analyses of Transcription Factors

Résumé

Yeast one-hybrid (Y1H) assay has been proven to be a powerful technique to characterize in vivo the interaction between a given transcription factor (TF), or its DNA-binding domain (DBD), and target DNA sequences. Comprehensive characterization of TF/DBD and DNA interactions should allow designing synthetic promoters that would undoubtedly be valuable for biotechnological approaches. Here, we use the ligation-independent cloning system (LIC) in order to enhance the cloning efficiency of DNA motifs into the pHISi Y1H vector. LIC overcomes important limitations of traditional cloning technologies, since any DNA fragment can be cloned into LIC compatible vectors without using restriction endonucleases, ligation, or in vitro recombination.
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Dates et versions

hal-01403405 , version 1 (25-11-2016)

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Zsolt Kelemen, Jonathan Przybyla-Toscano, Nicolas Tissot, Loic Lepiniec, Christian Dubos. Fast and Efficient Cloning of Cis-Regulatory Sequences for High-Throughput Yeast One-Hybrid Analyses of Transcription Factors. Plant Synthetic Promoters: Methods in Molecular Biology, Chapter 9, Springer Protocols, Humana Press, 2016, Methods in Molecular Biology, 978-1-4939-6394-2. ⟨10.1007/978-1-4939-6396-6_9⟩. ⟨hal-01403405⟩
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