ZFIN ID: ZDB-PUB-170308-15
Medaka vasa is required for migration but not survival of primordial germ cells
Li, M., Hong, N., Xu, H., Yi, M., Li, C., Gui, J., Hong, Y.
Date: 2009
Source: Mechanisms of Development   126(5-6): 366–381 (Journal)
Registered Authors: Gui, Jian-Fang, Yi, Meisheng
Keywords: none
MeSH Terms:
  • Animals
  • Base Sequence
  • Cell Movement*/drug effects
  • Cell Survival/drug effects
  • DEAD-box RNA Helicases/metabolism*
  • Embryo, Nonmammalian/cytology
  • Embryo, Nonmammalian/drug effects
  • Embryo, Nonmammalian/enzymology
  • Gene Expression Regulation, Developmental/drug effects
  • Gene Knockdown Techniques
  • Germ Cells/cytology*
  • Germ Cells/drug effects
  • Germ Cells/enzymology*
  • Models, Biological
  • Molecular Sequence Data
  • Oligonucleotides, Antisense/genetics
  • Oligonucleotides, Antisense/pharmacology
  • Oryzias/embryology
  • Oryzias/genetics
  • Oryzias/metabolism*
  • Phenotype
PubMed: 19249358 Full text @ Mech. Dev.
FIGURES
ABSTRACT
Vasa is essential for germline development. However, the precise processes in which vasa involves vary considerably in diverse animal phyla. Here we show that vasa is required for primordial germ cell (PGC) migration in the medakafish. vasa knockdown by two morpholinos led to the PGC migration defect that was rescued by coinjection of vasa RNA. Interestingly, vasa knockdown did not alter the PGC number, identity, proliferation and motility even at ectopic locations. We established a cell culture system for tracing PGCs at the single cell level in vitro. In this culture system, control and morpholino-injected gastrulae produced the same PGC number and the same time course of PGC survival. Importantly, vasa-depleted PGCs in culture had similar motility and locomotion to normal PGCs. Expression patterns of wt1a, sdf1b and cxcr4b in migratory tissues remained unchanged by vasa knockdown. By chimera formation we show that PGCs from vasa-depleted blastulae failed to migrate properly in the normal environment, whereas control PGCs migrated normally in vasa-disrupted embryos. Furthermore, ectopic PGCs in vasa-depleted embryos also retained all the PGC properties examined. Taken together, medaka vasa is cell-autonomously required for PGC migration, but dispensable to PGC proliferation, motility, identity and survival.
ADDITIONAL INFORMATION No data available