Table 2. Characteristics of genome editing technologies.
ZFNs | TALENs | CRISPR/Cas9 | |
---|---|---|---|
Length of recognized DNA target | 9–18bp | 30–40bp | 22bp + PAM sequence |
DNA recognition | Multimeric protein-DNA interaction | Protein-DNA interaction | RNA-DNA interaction |
Nuclease design | Difficult | Feasible | Easy |
Cost | High | Moderate | Low |
Success rate of nuclease design | Low | High | High |
Potential off-target effects | Yes | Yes | Yes |
Specificity | Moderate | High | Moderate |
Sensitivity to DNA methylation | Not known | Sensitive to CpG methylation | Not sensitive to CpG methylation |
CRISPR/Cas9: clustered regularly interspaced short palindromic repeats/CRISPR-associated proteins 9, PAM: protospacer adjacent motif, TALENs: transcription activator-like effector nucleases, ZFNs: zinc finger nucleases