(a) Natural structure of TALEs derived from Xanthomonas sp. Each DNA-binding module consists of 34 amino acids, where the
RVDs in the 12th and 13th amino acid positions of each repeat specify the DNA base being targeted according to the cipher NG = T, HD = C, NI = A, and NN = G or A. The DNA-binding modules are flanked by nonrepetitive N and C termini, which carry the
translocation, nuclear localization (NLS) and transcription activation (AD) domains. A cryptic signal within the N terminus
specifies a thymine as the first base of the target site.
(b) The TALE toolbox allows rapid and inexpensive construction of custom TALE-TFs and TALENs. The kit consists of 12 plasmids
in total: four monomer plasmids to be used as templates for PCR amplification, four TALE-TF and four TALEN cloning backbones
corresponding to four different bases targeted by the 0.5 repeat. CMV, cytomegalovirus promoter; N term, nonrepetitive N
terminus from the Hax3 TALE; C term, nonrepetitive C terminus from the Hax3 TALE; BsaI, type IIs restriction sites used for
the insertion of custom TALE DNA-binding domains; ccdB + CmR, negative selection cassette containing the ccdB negative
selection gene and chloramphenicol resistance gene; NLS, nuclear localization signal; VP64, synthetic transcriptional
activator derived from VP16 protein of herpes simplex virus; 2A, 2A self-cleavage linker; EGFP, enhanced green fluorescent
protein; polyA signal, polyadenylation signal; FokI, catalytic domain from the FokI endonuclease.
(c) TALEs can be used to generate custom TALE-TFs and modulate the transcription of endogenous genes from the genome. The
TALE DNA-binding domain is fused to the synthetic VP64 transcriptional activator, which recruits RNA polymerase and other factors needed to initiate transcription.
(d) TALENs can be used to generate site-specific double-strand breaks to facilitate genome editing through nonhomologous
repair or homology directed repair. Two TALENs target a pair of binding sites flanking a 16-bp spacer. The left and right
TALENs recognize the top and bottom strands of the target sites, respectively. Each TALE DNA-binding domain is fused to the
catalytic domain of FokI endonuclease; when FokI dimerizes, it cuts the DNA in the region between the left and right
TALEN-binding sites.
