The expression and stage-specific localization of protein kinase C isotypes during mouse preimplantation development

Christine M. Pauken, David Capco

Research output: Contribution to journalArticle

108 Scopus citations

Abstract

Signaling events mediate many processes that act during embryogenesis to initiate the program of early development. Within the cell many of these changes are mediated through the activation or inactivation of kinases and phosphatases. Protein kinase C (PKC) is one kinase that has been shown to be involved in at least two developmental transitions during early development, fertilization and embryonic compaction. PKC is a family of kinases whose various isotypes have differing requirements for activation of the kinase that include the availability of calcium, diacylglycerol, and negatively charged phospholipids. The presence of more than one isotype in an egg or blastomere of the embryo would provide the possibility that different isotypes mediate distinct signaling pathways in the cells. To address this possibility the different isotypes of PKC were examined at the mRNA and protein levels during preimplantation development in the mouse. Our results demonstrate that seven isotypes of PKC are present during preimplantation development in mouse, some are of maternal origin and others appear after fertilization. Two isotypes have a stage-dependent nuclear localization. In addition, within each blastomere PKC isotypes occupy different subcellular locations in a stage-dependent fashion. (C) 2000 Academic Press.

Original languageEnglish (US)
Pages (from-to)411-421
Number of pages11
JournalDevelopmental Biology
Volume223
Issue number2
DOIs
StatePublished - Jul 15 2000

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Keywords

  • Compaction
  • Early development
  • Embryogenesis
  • Mouse
  • Protein kinase C

ASJC Scopus subject areas

  • Molecular Biology
  • Developmental Biology
  • Cell Biology

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