(A) Scheme showing the transcription activator-like effector nuclease (TALEN) target site in the amotl2a locus with the left and right TALEN-binding sites in red separated by the spacer including the restriction site used for screening (blue) (top). Alignment of the two conserved amotl2a mutant alleles with the corresponding wild-type sequence showing the deleted nucleotides (bottom). (B) Scheme comparing the functional domains present in the wild-type Amotl2a protein (721aa long) and the putative truncated proteins (272aa +17 or +9 missense aa for allele fu45 and fu46, respectively). (C–F) 36 hpf cldnb:gfp wild-type sibling (C, D) or amotl2a−/− mutant embryo (E, F) imaged with fluorescent (C, E) or transmitted light (D, F). (G, H, J, K) MIP of Z-stacks of pLLP in cldnb:gfp embryos with the indicated genetic background. (I, L) Boxplots comparing the cell numbers between the indicated genetic backgrounds. (M, N) MZamotl2a−/− mutant embryo (N) showing an extra deposited neuromast as compared to a wild-type sibling embryo (M). (O) Boxplot showing the corresponding quantification (Figure 4—source data 1, 2; Figure 4—figure supplements 1, 2, Figure 4—source data 3, 4).
DOI:
http://dx.doi.org/10.7554/eLife.08201.017
Figure 4—source data 1. Cell counts in zygotic amotl2a mutants.
Figure 4—source data 2. Number of deposited neuromasts in MZamotl2a mutants.
Figure 4—source data 3. Migration speed in MZamotl2a mutants.
Figure 4—source data 4. Cell counts in neuromasts of morphants (Excel sheet 1 related to panel A) and MZamotl2a mutants (Excel sheet 2 related to panel B).