SMAD1 signaling is critical for initial commitment of germ cell lineage from mouse epiblast

Mech Dev. 2002 Oct;118(1-2):99-109. doi: 10.1016/s0925-4773(02)00237-x.

Abstract

Commitment of the germ cell lineage during embryogenesis depends on zygotic gene expression in mammals, but little is known about the signaling molecules required for germ cell formation. Here we show that the intracellular signaling molecule SMAD1, acting downstream of bone morphogenetic protein (BMP) receptors, is required for the commitment of germ cell lineage from epiblast in early mouse embryos. Smad1 homozygous mutant embryos (Smad1-/-) were generated by in-frame insertion of lacZ gene into an exon of the Smad1 gene. Most of the Smad1-/- embryos contained no primordial germ cells (PGCs) and had short allantois, while histological analysis and in situ hybridization for the mesoderm marker genes revealed that early mesoderm induction was normal in those embryos. Smad1 expression was observed in epiblast and in visceral endoderm during gastrulation, while only a few alkaline phosphatase-positive PGCs at 7.5 and 8.5 days post coitum (E7.5 and E8.5) expressed Smad1. Phosphorylated SMAD proteins were localized in the proximal region of epiblast at E6.0-6.5, where the progenitors of PGCs and of allantois reside. Single-cell reverse transcription-polymerase chain reaction analysis revealed that the expression of Smad1, -5 and -8 were sporadic and mutually independent in proximal epiblast cells. We also found that BMP4-induced differentiation of PGCs from epiblast in vitro was fully dependent on the existence of phosphorylated SMAD1. These results indicate that SMAD1 signaling possesses a critical and non-redundant function in the initial commitment of the germ cell lineage.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkaline Phosphatase / metabolism
  • Animals
  • Cell Lineage
  • Central Nervous System / embryology
  • DNA-Binding Proteins / genetics*
  • DNA-Binding Proteins / metabolism*
  • Dose-Response Relationship, Drug
  • Exons
  • Gene Expression Regulation, Developmental*
  • Genotype
  • Heterozygote
  • Homozygote
  • Immunohistochemistry
  • In Situ Hybridization
  • Lac Operon
  • Mesoderm / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred DBA
  • Models, Genetic
  • Mutagenesis, Site-Directed
  • Oligonucleotides, Antisense / pharmacology
  • Phosphoproteins / metabolism
  • Phosphorylation
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction*
  • Smad Proteins
  • Smad1 Protein
  • Smad5 Protein
  • Time Factors
  • Tissue Distribution
  • Trans-Activators / genetics*
  • Trans-Activators / metabolism*

Substances

  • DNA-Binding Proteins
  • Oligonucleotides, Antisense
  • Phosphoproteins
  • Smad Proteins
  • Smad1 Protein
  • Smad1 protein, mouse
  • Smad5 Protein
  • Smad5 protein, mouse
  • Trans-Activators
  • Alkaline Phosphatase