Migration of Kupffer’s vesicle derived cells is essential for tail morphogenesis in zebrafish embryos

Abstract

A phenotypic screen of fungal filtrates on developing zebrafish embryos identified metabolites from the fungusCeratocystis populicolato induce ectopic tail formation, including a split notochord and a duplicated caudal fin. Chemical analyses led to the identification of monoterpene alcohols, in particular geraniol, as active compounds inducing ectopic tail formation during a specific 4 h time window during tail bud stage. Embryos from Tüpfel long fin zebrafish (TL) were more susceptible to ectopic tail formation by geraniol than embryos from Wild Indian Karyotpe (WIK) zebrafish, indicating zebrafish strain specificity. RNA sequencing on tail buds of 15-somite stage embryos revealed downregulation of essential genes of the retinoic acid signaling pathway and differential expression ofcyp26a1andfgf8aand downstreamhox-genes was validated. Time-lapse imaging revealed that Kupffer’s vesicle derived cells failed to migrate shorty after Kupffer’s vesicle collapse upon geraniol treatment and these cells failed to merge with progenitors from the tail bud. Instead, these cells contributed to an ectopic tail, expressing markers for presomitic mesoderm, somite and notochord tissue. Taken together, our data suggests that Kupffer’s vesicle cells harbor tail progenitor capacity, and proper migration of these cells is essential for normal tail morphogenesis.Summary StatementInhibition of Kupffer’s vesicle derived cell migration affected tail morphogenesis and resulted in ectopic tail formation in zebrafish embryos.