Figures
In Fig 4, there is an error in panel C. The label of x-axis for the bar plot of Fig 4C should have been M5, M6, M7. Please see the correct Fig 4 here.
(A) Subcloned sequences belonging to A. ocellaris juveniles (clutch 11, sgRNA RH2B 4) with mutations at targeted sequences (underlined) located on Exon 1 of the RH2B opsin gene. Wildtype (WT) sequence is included for reference. Mutations included deletions (dashes), substitutions (green), and insertions (blue). Sequence labels on the left-side indicate mutant fish and allele no., while numbers on the right-side indicate the base pair change (Δbp) and the proportion of each allele out of the total number of cloned sequences for each fish. (B) Images of the RH2B mutant A. ocellaris juveniles. (C) Number of frameshift and in-frame mutations per RH2B mutant fish.
Reference
- 1. Mitchell LJ, Tettamanti V, Rhodes JS, Marshall NJ, Cheney KL, Cortesi F (2021) CRISPR/Cas9-mediated generation of biallelic F0 anemonefish (Amphiprion ocellaris) mutants. PLOS ONE 16(12): e0261331. https://doi.org/10.1371/journal.pone.0261331
Citation: Mitchell LJ, Tettamanti V, Rhodes JS, Marshall NJ, Cheney KL, Cortesi F (2024) Correction: CRISPR/Cas9-mediated generation of biallelic F0 anemonefish (Amphiprion ocellaris) mutants. PLoS ONE 19(6): e0305644. https://doi.org/10.1371/journal.pone.0305644
Published: June 12, 2024
Copyright: © 2024 Mitchell et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.