C. elegans pro-1 activity is required for soma/germline interactions that influence proliferation and differentiation in the germ line

Development. 2004 Mar;131(6):1267-78. doi: 10.1242/dev.01002. Epub 2004 Feb 18.

Abstract

Strict spatial and temporal regulation of proliferation and differentiation is essential for proper germline development and often involves soma/germline interactions. In C. elegans, a particularly striking outcome of defective regulation of the proliferation/differentiation pattern is the Pro phenotype in which an ectopic mass of proliferating germ cells occupies the proximal adult germ line, a region normally occupied by gametes. We describe a reduction-of-function mutation in the gene pro-1 that causes a highly penetrant Pro phenotype. The pro-1 mutant Pro phenotype stems from defects in the time and position of the first meiotic entry during early germline development. pro-1(RNAi) produces a loss of somatic gonad structures and concomitant reduction in germline proliferation and gametogenesis. pro-1 encodes a member of a highly conserved subfamily of WD-repeat proteins. pro-1(+) is required in the sheath/spermatheca lineage of the somatic gonad in its role in the proper establishment of the proliferation/differentiation pattern in the germline. Our results provide a handle for further analysis of this soma-to-germline interaction.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Caenorhabditis elegans / embryology
  • Caenorhabditis elegans / metabolism*
  • Caenorhabditis elegans Proteins*
  • Cell Differentiation / physiology*
  • Cell Division / physiology
  • Contractile Proteins / genetics
  • Contractile Proteins / metabolism*
  • Genes, Reporter
  • Germ Cells / metabolism*
  • Gonads / embryology
  • Gonads / metabolism
  • Meiosis / physiology
  • Membrane Glycoproteins / metabolism
  • Microfilament Proteins / genetics
  • Microfilament Proteins / metabolism*
  • Phenotype
  • Profilins
  • Receptors, Notch
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Sequence Deletion

Substances

  • Caenorhabditis elegans Proteins
  • Contractile Proteins
  • Glp-1 protein, C elegans
  • Membrane Glycoproteins
  • Microfilament Proteins
  • Profilins
  • Receptors, Notch
  • Recombinant Fusion Proteins