Programmable Sequence-Specific Transcriptional Regulation of Mammalian Genome Using Designer TAL Effectors
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Zhang Nature Biotechnology 2011.pdf
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Author(s) • • • • •
Zhang, Feng
Cong, Le
Lodato, Simona
Kosuri, Sriram
Church, George M.
Arlotta, Paola
Date Issued
January 2011
Journal
Nature Biotechnology
Publisher
Nature Publishing Group
Citation
Zhang, Feng et al. “Efficient Construction of Sequence-specific TAL Effectors for Modulating Mammalian Transcription.” Nature Biotechnology 29.2 (2011): 149–153. Web.
Version
Author's final manuscript
Abstract
The ability to direct functional proteins to specific DNA sequences is a long-sought goal in the study and engineering of biological processes. Transcription activator–like effectors (TALEs) from Xanthomonas sp. are site-specific DNA-binding proteins that can be readily designed to target new sequences. Because TALEs contain a large number of repeat domains, it can be difficult to synthesize new variants. Here we describe a method that overcomes this problem. We leverage codon degeneracy and type IIs restriction enzymes to generate orthogonal ligation linkers between individual repeat monomers, thus allowing full-length, customized, repeat domains to be constructed by hierarchical ligation. We synthesized 17 TALEs that are customized to recognize specific DNA-binding sites, and demonstrate that they can specifically modulate transcription of endogenous genes (SOX2 and KLF4) in human cells.
MIT Department
Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences
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Creative Commons Attribution-Noncommercial-Share Alike 3.0
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DOI of Published Version
https://doi.org/10.1038/nbt.1775