Reverse Genetic Screening Reveals Poor Correlation between Morpholino-Induced and Mutant Phenotypes in Zebrafish
Messenger
Blotting, Western
Oligonucleotides
Embryonic Structures
Real-Time Polymerase Chain Reaction
Morpholinos
Molecular Genetics
03 medical and health sciences
Research Support, N.I.H., Extramural
Journal Article
Animals
Developmental
RNA, Messenger
Antisense
Zebrafish
Cancer Biology
0303 health sciences
Deoxyribonucleases
Blotting
Reverse Transcriptase Polymerase Chain Reaction
Research Support, Non-U.S. Gov't
Gene Expression Regulation, Developmental
Oligonucleotides, Antisense
Zebrafish Proteins
Phenotype
Gene Expression Regulation
Gene Knockdown Techniques
Mutation
RNA
Western
Developmental Biology
DOI:
10.1016/j.devcel.2014.11.018
Publication Date:
2014-12-19T20:51:08Z
AUTHORS (17)
ABSTRACT
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.
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