The biology of the germ line in echinoderms

Mol Reprod Dev. 2014 Aug;81(8):679-711. doi: 10.1002/mrd.22223. Epub 2014 Jul 22.

Abstract

The formation of the germ line in an embryo marks a fresh round of reproductive potential. The developmental stage and location within the embryo where the primordial germ cells (PGCs) form, however, differs markedly among species. In many animals, the germ line is formed by an inherited mechanism, in which molecules made and selectively partitioned within the oocyte drive the early development of cells that acquire this material to a germ-line fate. In contrast, the germ line of other animals is fated by an inductive mechanism that involves signaling between cells that directs this specialized fate. In this review, we explore the mechanisms of germ-line determination in echinoderms, an early-branching sister group to the chordates. One member of the phylum, sea urchins, appears to use an inherited mechanism of germ-line formation, whereas their relatives, the sea stars, appear to use an inductive mechanism. We first integrate the experimental results currently available for germ-line determination in the sea urchin, for which considerable new information is available, and then broaden the investigation to the lesser-known mechanisms in sea stars and other echinoderms. Even with this limited insight, it appears that sea stars, and perhaps the majority of the echinoderm taxon, rely on inductive mechanisms for germ-line fate determination. This enables a strongly contrasted picture for germ-line determination in this phylum, but one for which transitions between different modes of germ-line determination might now be experimentally addressed.

Publication types

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

MeSH terms

  • Animals
  • Asymmetric Cell Division / physiology
  • Calcium / metabolism
  • Calcium Channels, L-Type / metabolism
  • DEAD-box RNA Helicases / metabolism
  • Echinodermata / embryology*
  • Embryonic Induction / physiology*
  • Endoplasmic Reticulum / metabolism
  • Gametogenesis / physiology*
  • Gene Expression Regulation, Developmental / physiology*
  • Germ Cells / physiology*
  • Models, Biological*
  • Signal Transduction / physiology*
  • Species Specificity

Substances

  • Calcium Channels, L-Type
  • DEAD-box RNA Helicases
  • Calcium