Extended Data Fig. 10: Characterization of the editing efficiency, nuclear genome-wide mutation and cellular toxicity induced by engineered TALEDs. | Nature Biotechnology

Extended Data Fig. 10: Characterization of the editing efficiency, nuclear genome-wide mutation and cellular toxicity induced by engineered TALEDs.

From: Leveraging base excision repair for efficient adenine base editing of mitochondrial DNA

Extended Data Fig. 10: Characterization of the editing efficiency, nuclear genome-wide mutation and cellular toxicity induced by engineered TALEDs.The alternative text for this image may have been generated using AI.

a, Schematic of the constructions of sTALED, esTALED6 and esTALED6R targeting mtDNA. b, Heatmaps of A-to-G editing frequencies induced by the indicated editors. The sequences of the TALE-binding regions are in blue, and bystander editing can be found in the boxes with dashed black lines. The boxes with dashed blue lines represent the narrowed editing windows. c and d, Number of A/T-to-G/C (c) and C/G-to-T/A (d) nuclear genome-wide substitutions induced by the indicated editors. e and f, Cell viability was measured by MTS assay at day 2 (e) and day 4 (f) post-transfection after treated with the indicated editors targeting ND1 site. For b, e and f, the data are presented as the mean ± s.d. from three independent experiments. For c and d, the eGFP data are presented as the mean ± s.d. from two independent experiments, sTALED, esTALED6 and esTALED6R are presented as the mean ± s.d. from three independent experiments. Statistical analysis was performed via two-tailed Student’s t-test. For e and f, statistical analysis was performed via two-tailed Welch’s t-test.

Back to article page