A genome-wide study of gene activity reveals developmental signaling pathways in the preimplantation mouse embryo

Dev Cell. 2004 Jan;6(1):133-44. doi: 10.1016/s1534-5807(03)00404-0.

Abstract

The preimplantation development of the mammalian embryo encompasses a series of critical events: the transition from oocyte to embryo, the first cell divisions, the establishment of cellular contacts, the first lineage differentiation-all the first subtle steps toward a future body plan. Here, we use microarrays to explore gene activity during preimplantation development. We reveal robust and dynamic patterns of stage-specific gene activity that fall into two major phases, one up to the 2-cell stage (oocyte-to-embryo transition) and one after the 4-cell stage (cellular differentiation). The mouse oocyte and early embryo express components of multiple signaling pathways including those downstream of Wnt, BMP, and Notch, indicating that conserved regulators of cell fate and pattern formation are likely to function at the earliest embryonic stages. Overall, these data provide a detailed temporal profile of gene expression that reveals the richness of signaling processes in early mammalian development.

Publication types

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

MeSH terms

  • Animals
  • Blastocyst / cytology
  • Blastocyst / metabolism*
  • Body Patterning / genetics*
  • Bone Morphogenetic Proteins / genetics
  • Cell Differentiation / genetics*
  • Cell Lineage / genetics
  • Cell Polarity / genetics
  • DNA Fingerprinting
  • Female
  • Fetus
  • Gene Expression Regulation, Developmental / genetics*
  • Genome
  • Male
  • Membrane Proteins / genetics
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred CBA
  • Oligonucleotide Array Sequence Analysis
  • Proto-Oncogene Proteins / genetics
  • RNA, Messenger, Stored / genetics
  • Receptors, Notch
  • Signal Transduction / genetics*
  • Time Factors
  • Totipotent Stem Cells / cytology
  • Totipotent Stem Cells / metabolism
  • Wnt Proteins
  • Zebrafish Proteins*
  • Zygote / cytology
  • Zygote / metabolism*

Substances

  • Bone Morphogenetic Proteins
  • Membrane Proteins
  • Proto-Oncogene Proteins
  • RNA, Messenger, Stored
  • Receptors, Notch
  • Wnt Proteins
  • Zebrafish Proteins