Regulation of DNA synthesis at the first cell cycle in the sea urchin in vivo

Methods Mol Biol. 2014:1128:223-36. doi: 10.1007/978-1-62703-974-1_15.

Abstract

Using fluorescent and non-fluorescent recombinant proteins has proved to be a very successful technique for following postfertilization events, in both male and female pronuclei during the first cell cycle of sea urchin in vivo. Proteins and dyes are introduced by microinjection into the unfertilized egg, and their function can be monitored by fluorescence or confocal/two-photon (2P) and transmitted light microscopy after insemination. Here, we describe expression and purification of GFP/RFP-tagged proteins involved in regulation of DNA replication. We also explain the techniques used to introduce recombinant proteins and fluorescent tubulin into sea urchin eggs and embryos.

MeSH terms

  • Animals
  • Cell Cycle
  • Cell Nucleus / metabolism
  • DNA Replication*
  • Escherichia coli
  • Female
  • Fertilization
  • Fluorescent Dyes / chemistry
  • Fluorescent Dyes / isolation & purification
  • Green Fluorescent Proteins / biosynthesis
  • Green Fluorescent Proteins / chemistry
  • Green Fluorescent Proteins / isolation & purification
  • Male
  • Microinjections
  • Microscopy, Confocal
  • Microscopy, Fluorescence
  • Ovum / cytology
  • Proliferating Cell Nuclear Antigen / biosynthesis
  • Proliferating Cell Nuclear Antigen / chemistry
  • Proliferating Cell Nuclear Antigen / isolation & purification
  • Sea Urchins / cytology*
  • Sea Urchins / physiology
  • Staining and Labeling
  • Tubulin / chemistry

Substances

  • Fluorescent Dyes
  • Proliferating Cell Nuclear Antigen
  • Tubulin
  • Green Fluorescent Proteins