PT  - JOURNAL ARTICLE
AU  - Cara E. Moravec
AU  - Gabriella C. Voit
AU  - Jarred Otterlee
AU  - Francisco Pelegri
TI  - Identification of Maternal-Effect Genes in Zebrafish using Maternal Crispants
AID  - 10.1101/2021.02.19.432057
DP  - 2021 Jan 01
TA  - bioRxiv
PG  - 2021.02.19.432057
4099  - http://biorxiv.org/content/early/2021/02/19/2021.02.19.432057.short
4100  - http://biorxiv.org/content/early/2021/02/19/2021.02.19.432057.full
AB  - In animals, early development is dependent on a pool of maternal factors, both RNA and proteins, which are required for basic cellular process and cell differentiation until zygotic genome activation. The role of a majority of these maternally expressed factors in adult fertility and early development is not fully understood. By exploiting the biallelic editing ability of CRISPR-Cas9 and the benefits of the zebrafish model, we identify and characterize maternal-effect genes in a single generation, using a maternal crispant technique. We validated the ability to generate biallelic mutations in the germline by creating maternal crispants that phenocopied previously characterized maternal-effect genes: motley/birc5b, tmi/prc1l, and aura/mid1ip1. Additionally, by targeting maternally expressed genes of unknown function in zebrafish, we identified two new maternal-effect zebrafish genes, kpna7 and fhcd3. The genetic identity of these maternal crispants was confirmed by sequencing haploid progeny from F0 females, which allowed the sequence analysis of newly induced lesions in the maternal germ line. Analysis of the induced lesions shows minimal genetic variation within a clutch, with an average of two edited alleles per clutch. These findings are consistent with biallelic editing events occurring in germ cells or their precursors of early CRISPR-Cas9-injected embryos, leading to maternal-effect phenotypes in the offspring. Our studies show that maternal crispants allow for the effective identification and primary characterization of maternal-effect genes in a single generation, facilitating the reverse genetics analysis of maternal factors that drive embryonic development.Competing Interest StatementThe authors have declared no competing interest.