FIGURE

Fig. S5

ID
ZDB-FIG-180712-16
Publication
Letelier et al., 2018 - Evolutionary emergence of the rac3b/rfng/sgca regulatory cluster refined mechanisms for hindbrain boundaries formation.
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Fig. S5

rac3b loss-of-function strategies. (A) Scheme depicting the structure of the zebrafish rac3b transcript showing the following: the position of the two different intron 4 splice-blocking morpholinos (in red) with the corresponding primers to assess the efficiency of the MOs (Primer-MO Fw/Rv; in green), the position of sgRNAs designed for CRISPR-Cas9 gene edition (sgRNA1/2; in blue), and the position of the screening primers (Primer-CRISPR Fw/Rv; in green). (B) Sequence showing mutations induced in rac3b by CRISPR-Cas9 genome edition (rac3b−/−). Generated indels (in blue) produce a premature stop codon (in red) that disrupts the reading frame. Intron 1 is shown in lowercase and exon 2 in uppercase. (C) Agarose gel showing the aberrant splicing products induced by morpholinos as detected by RT-PCR from embryos injected with MO-Control, MO-rac3bSBE4I4, or MO-rac3bSBI4E5. MO-rac3bSBE4I4 generated inclusion of intron 4 (+113) and skipping of exon 4 (−63); MO-rac3bSBI4E5 resulted in the retention of intron 4 (+113). Both MOs reduced the relative amount of WT transcript compared with the control. (D) WT (rac3b+/+) and CRISPR-rac3b homozygous mutant (rac3b−/−) embryos at 24 hpf. At this stage, mutants show a normal appearance with a diminished eye area quantified in E. (E) Box plot showing eye area at 24 hpf of rac3b+/+ and rac3b−/− embryos from three independent clutches (unpaired t test, ****P < 0.0001). (F) rac3b−/− embryos incubated at 36 °C (from 8 hpf onward) display curled body axis at 54 hpf (G) and 78 hpf (H), compared with rac3b+/+ embryos. (G and H) Box plot representation of body angle measurements of rac3b+/+ and rac3b−/− larvae at different stages: 54 hpf (unpaired t test, ****P < 0.0001) and 78 hpf (unpaired t test, ****P < 0.0001). (I) rac3b−/− embryos incubated at higher temperatures (40 °C) display increased lethality rate compared with rac3b+/+ (two-way ANOVA, *P < 0.05 and ****P < 0.0001). For rac3b+/+, n = 720 embryos from four independent clutches; for rac3b−/−, n = 1,080 embryos from six independent clutches. All of the experiments were performed using stable lines.

Expression Data

Expression Detail
Antibody Labeling
Phenotype Data
Fish:
Condition:
Observed In:
Stage Range: Prim-5 to Protruding-mouth

Phenotype Detail
Acknowledgments
This image is the copyrighted work of the attributed author or publisher, and ZFIN has permission only to display this image to its users. Additional permissions should be obtained from the applicable author or publisher of the image. Full text @ Proc. Natl. Acad. Sci. USA