Decreased expression of mitochondrial genes in human unfertilized oocytes and arrested embryos

Fertil Steril. 2004 Mar:81 Suppl 1:912-8. doi: 10.1016/j.fertnstert.2003.11.013.

Abstract

Objective: To evaluate the relationship between mitochondrial gene expression of oocytes/embryos and their fertilizability in unfertilized oocytes, arrested embryos, and tripronucleate zygotes, because both nuclear and cytoplasmic factors contribute to oocyte activation, fertilization, and subsequent development.

Design: Prospective laboratory research.

Setting: In vitro fertilization (IVF) laboratory in a university hospital.

Patient(s): Seventy-five unfertilized oocytes, 45 arrested embryos, and 24 tripronucleate (3PN) embryos from 45 female patients undergoing IVF.

Intervention(s): Analysis of mitochondrial gene expression by semiquantitative reverse transcription polymerase chain reaction (RT-PCR).

Main outcome measure(s): Comparison of the expression levels of mitochondrial genes including ND2, CO I, CO II, ATPase 6, CO III, ND3, ND6, and Cyt b in three groups.

Result(s): Significantly decreased transcription levels were expressed in unfertilized oocytes and arrested embryos. The average expression levels of the eight determined genes compared with the control (GAPDH) was 4.4 +/- 0.7, 6.4 +/- 1.1, and 13.2 +/- 1.1 in unfertilized oocytes, arrested embryos, and 3PN embryos, respectively. Significantly decreased expressions of the ATPase 6, CO III, and ND3 genes were detected from samples with 4977-bp common deletion in the mitochondrial DNA (mtDNA) compared with the non-deletion group.

Conclusion(s): The present study is the first report to present globally decreased mitochondrial gene expression levels in human compromised oocytes and embryos. These data support the notion that the down-regulation of mitochondrial RNA by defective oxidative phosphorylation genes possibly affects oocyte quality including fertilization and further embryo development.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • DNA, Mitochondrial / genetics
  • Down-Regulation*
  • Embryo, Mammalian / physiology*
  • Female
  • Gene Deletion
  • Gene Expression*
  • Humans
  • Mitochondria / genetics*
  • Molecular Sequence Data
  • Oocytes / physiology*
  • Prospective Studies
  • Reverse Transcriptase Polymerase Chain Reaction
  • Transcription, Genetic

Substances

  • DNA, Mitochondrial