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Updated: Aug 9, 2026

Meiotic Spindle Assessment in Mouse Oocytes by siRNA-mediated Silencing
Published on: October 11, 2015
Decreased expression of mitochondrial genes in human unfertilized oocytes and arrested embryos
Rong-Hong Hsieh1, Heng-Kien Au, Tien-Shun Yeh
1Department of Obstetrics and Gynecology, Taipei Medical University Hospital, 250 Wu-Hsing Street, Taipei, Taiwan 110, Republic of China..
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.
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