IMAGE

Fig. 5

ID: ZDB-IMAGE-200130-11
Publication: Huning et al., 2020 - Two paralogous znf143 genes in zebrafish encode transcriptional activator proteins with similar functions but expressed at different levels during early development
All Figures: Figures for Huning et al., 2020

Image

Figure Caption

Fig. 5

CRISPRi knockdown of either znf143a or znf143b induce brain developmental defects. a. Diagram showing targets for sgRNAs. Numbered boxes indicate positions of exons. b. One-cell zebrafish embryos were injected with sgRNA/dCas9 protein complexes to knock down znf143a, znf143b, or in control experiments with dCas9 protein only (−sgRNA) and observed at 24hpf. Representative photographs of abnormal brain phenotypes are shown, with circled regions showing the areas of most interest. c. Consistent phenotypes are grouped into classes. Severe phenotypes lacked axial development. 159 embryos were counted for the control injections lacking any sgRNAs, 132 embryos were counted for the znf143a CRISPRi injections, and 136 embryos were counted for the znf143b CRISPRi injections

Figure Data

Phenotype details

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 @ BMC Mol Cell Biol