ZFIN ID: ZDB-PUB-141224-21
Reverse Genetic Screening Reveals Poor Correlation between Morpholino-Induced and Mutant Phenotypes in Zebrafish
Kok, F.O., Shin, M., Ni, C., Gupta, A., Grosse, A.S., van Impel, A., Kirchmaier, B.C., Peterson-Maduro, J., Kourkoulis, G., Male, I., DeSantis, D.F., Sheppard-Tindell, S., Ebarasi, L., Betsholtz, C., Schulte-Merker, S., Wolfe, S.A., Lawson, N.D.
Date: 2015
Source: Developmental Cell 32(1): 97-108 (Journal)
Registered Authors: Betsholtz, Christer, Ebarasi, Lwaki, Gupta, Ankit, Kourkoulis, George D., Lawson, Nathan, Peterson-Maduroe, Josi, Schulte-Merker, Stefan, Shin, Masahiro, Wolfe, Scot A., van Impel, Andreas
Keywords: none
MeSH Terms: Animals; Blotting, Western; Deoxyribonucleases/genetics*; Deoxyribonucleases/metabolism; Gene Expression Regulation/drug effects*; Gene Expression Regulation, Developmental; Gene Knockdown Techniques/methods*; Morpholinos/pharmacology*; Mutation/genetics*; Oligonucleotides, Antisense/pharmacology*; Phenotype; RNA, Messenger/genetics; Real-Time Polymerase Chain Reaction; Reverse Transcriptase Polymerase Chain Reaction; Zebrafish/genetics*; Zebrafish/growth & development; Zebrafish Proteins/antagonists & inhibitors; Zebrafish Proteins/genetics*
PubMed: 25533206 Full text @ Dev. Cell
FIGURES   (current status)
The widespread availability of programmable site-specific nucleases now enables targeted gene disruption in the zebrafish. In this study, we applied site-specific nucleases to generate zebrafish lines bearing individual mutations in more than 20 genes. We found that mutations in only a small proportion of genes caused defects in embryogenesis. Moreover, mutants for ten different genes failed to recapitulate published Morpholino-induced phenotypes (morphants). The absence of phenotypes in mutant embryos was not likely due to maternal effects or failure to eliminate gene function. Consistently, a comparison of published morphant defects with the Sanger Zebrafish Mutation Project revealed that approximately 80% of morphant phenotypes were not observed in mutant embryos, similar to our mutant collection. Based on these results, we suggest that mutant phenotypes become the standard metric to define gene function in zebrafish, after which Morpholinos that recapitulate respective phenotypes could be reliably applied for ancillary analyses.