Nanos functions to maintain the fate of the small micromere lineage in the sea urchin embryo

Dev Biol. 2010 Jan 15;337(2):220-32. doi: 10.1016/j.ydbio.2009.10.030. Epub 2009 Oct 28.

Abstract

The translational regulator nanos is required for the survival and maintenance of primordial germ cells during embryogenesis. Three nanos homologs are present in the genome of the sea urchin Strongylocentrotus purpuratus, all of which are expressed with different timing in the small micromere lineage. This lineage is set-aside during embryogenesis and contributes to constructing the adult rudiment. Small micromeres lacking Sp-nanos1 and Sp-nanos2 undergo an extra division and are not incorporated into the coelomic pouches. Further, these cells do not accumulate Vasa protein even though they retain vasa mRNA. Larvae that develop from Sp-nanos1 and 2 knockdown embryos initially appear normal, but do not develop adult rudiments; although they are capable of eating, over time they fail to grow and eventually die. We conclude that the acquisition and maintenance of multipotency in the small micromere lineage requires nanos, which may function in part by repressing the cell cycle and regulating other multipotency factors such as vasa. This work, in combination with other recent results in Ilyanassa and Platynereis dumerilii, suggests the presence of a conserved molecular program underlying both primordial germ cell and multipotent cell specification and maintenance.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Cell Count
  • Cell Lineage* / drug effects
  • DEAD-box RNA Helicases / metabolism
  • Embryo, Nonmammalian / cytology*
  • Embryo, Nonmammalian / drug effects
  • Embryo, Nonmammalian / enzymology
  • Gastrula / cytology
  • Gastrula / drug effects
  • Gastrula / metabolism
  • Gene Expression Regulation, Developmental / drug effects
  • Gene Knockdown Techniques
  • Larva / cytology
  • Larva / drug effects
  • Models, Biological
  • Molecular Sequence Data
  • Oligonucleotides, Antisense / pharmacology
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • RNA-Binding Proteins / chemistry
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / metabolism*
  • Sea Urchins / cytology
  • Sea Urchins / drug effects
  • Sea Urchins / embryology*
  • Sea Urchins / genetics
  • Sequence Homology, Amino Acid

Substances

  • Oligonucleotides, Antisense
  • RNA, Messenger
  • RNA-Binding Proteins
  • DEAD-box RNA Helicases