FIGURE

Fig. S7

ID
ZDB-FIG-180827-43
Publication
Astone et al., 2018 - Zebrafish mutants and TEAD reporters reveal essential functions for Yap and Taz in posterior cardinal vein development
Other Figures
All Figure Page
Back to All Figure Page
Fig. S7

CRISPR targeted mutagenesis of the zebrafish yap1 and taz loci.

Single guide RNAs (sgRNAs) were designed to target the first exon of yap1 and the second exon of taz. Sequence alignments between WT and mutant sequences for yap1bns19 (A) and tazbns35 (B). The underlined nucleotides are the PAM sequences. (A’ and B’) These indel mutations result in a frameshift and are predicted to encode a truncated protein product as represented in the cartoon. (A’’ and B’’) The genotyping of these alleles can be performed by simple PCR followed by resolution of the WT and mutant amplicons by gel electrophoresis. (C) Representative confocal images of Tg(Hsa.CTGF:nlsmCherry);TgBAC(etv2:EGFP) transgenic embryos in yap and taz mutant background. Higher magnification images correspond to the region demarcated in yellow. (C’) The mCherry fluorescence was measured in the endothelial cells and normalized for the GFP fluorescence used as internal standard. n for each group is indicated. * = p<0.05.

Expression Data

Expression Detail
Antibody Labeling
Phenotype Data

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 @ Sci. Rep.