Expression of Cu/Zn and Mn superoxide dismutases during bovine embryo development: influence of in vitro culture

Mol Reprod Dev. 2001 Jan;58(1):45-53. doi: 10.1002/1098-2795(200101)58:1<45::AID-MRD7>3.0.CO;2-J.

Abstract

Temporal pattern of expression of Cu/Zn and Mn superoxide dismutases (SODs) was investigated in bovine oocytes and embryos produced in vitro in two different culture conditions and in vivo after superovulation. SODs were examined at a transcriptional level in single oocytes and embryos by reverse transcriptase-polymerase chain reaction (RT-PCR) and, at a protein level, by Western blotting on pools of embryos. mRNA encoding Cu/Zn SOD were detected in in vitro bovine embryos throughout preattachment development as well as in in vivo derived morulae and blastocysts. Transcripts for Mn SOD gene were detected in most immature and in vitro matured oocytes as well as in some zygotes and 5- to 8-cell embryos while no transcript was found at the 9-to 16-cell stage in both culture conditions. In vitro embryonic expression of Mn SOD was detected earlier in the presence of serum. Half of the morulae showed the transcript if cultured with 5% serum while none without serum. At the blastocyst stage Mn SOD could be detected independently of culture conditions. For in vivo-derived embryos Mn SOD transcripts were detected both in morulae and blastocysts. Immunoblotting analyses revealed that Cu/Zn SOD and Mn SOD were also present at a protein level in in vitro-derived zygotes and blastocysts. Together these data demonstrate, for the first time, that Mn SOD is transcribed and that Cu/Zn and Mn SOD proteins are expressed in preimplantation bovine embryos. Finally, they suggest that Mn SOD transcription is altered by in vitro culture conditions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Cattle
  • Cells, Cultured
  • DNA, Complementary
  • Embryonic and Fetal Development*
  • Fallopian Tubes / cytology
  • Female
  • Free Radical Scavengers
  • In Vitro Techniques
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Superoxide Dismutase / biosynthesis*
  • Superoxide Dismutase / genetics
  • Transcription, Genetic

Substances

  • DNA, Complementary
  • Free Radical Scavengers
  • RNA, Messenger
  • Superoxide Dismutase