Clin Exp Reprod Med.  2011 Jun;38(2):68-74. 10.5653/cerm.2011.38.2.68.

Changes in gene expression associated with oocyte meiosis after Obox4 RNAi

Affiliations
  • 1Department of Biomedical Science, College of Life Science, CHA University, Seoul, Korea. leeka@ovary.co.kr
  • 2CHA Research Institute, CHA University, Seoul, Korea.

Abstract


OBJECTIVE
Previously, we found that oocyte specific homeobox (Obox) 4 plays significant role in completion of meiosis specifically at meiosis I-meiosis II (MI-MII) transition. The purpose of this study was to determine the mechanism of action of Obox4 in oocyte maturation by evaluating downstream signal networking.
METHODS
The Obox4 dsRNA was prepared by in vitro transcription and microinjected into the cytoplasm of germinal vesicle oocytes followed by in vitro maturation in the presence or absence of 0.2 mM 3-isobutyl-1-metyl-xanthine. Total RNA was extracted from 200 oocytes of each group using a PicoPure RNA isolation kit then amplified two-rounds. The probe hybridization and data analysis were used by Affymetrix GeneChip(R) Mouse Genome 430 2.0 array and GenPlex 3.0 (ISTECH, Korea) software, respectively.
RESULTS
Total 424 genes were up (n=80) and down (n=344) regulated after Obox4 RNA interference (RNAi). Genes mainly related to metabolic pathways and mitogen-activated protein kinase (MAPK) signaling pathway was changed. Among the protein kinase C (PKC) isoforms, PKC-alpha, beta, gamma were down-regulated and especially the MAPK signaling pathway PKC-gamma was dramatically decreased by Obox4 RNAi. In the cell cycle pathway, we evaluated the expression of genes involved in regulation of chromosome separation, and found that these genes were down-regulated. It may cause the aberrant chromosome segregation during MI-MII transition.
CONCLUSION
From the results of this study, it is concluded that Obox4 is important upstream regulator of the PKC and anaphase-promoting complex action for maintaining intact germinal vesicle.

Keyword

Oocyte Maturation; Obox4, Mouse; RNA Interference; Microarray Analysis

MeSH Terms

Animals
Cell Cycle
Chimera
Chromosome Segregation
Cytoplasm
Gene Expression
Genes, Homeobox
Genome
Meiosis
Metabolic Networks and Pathways
Mice
Microarray Analysis
Oocytes
Protein Isoforms
Protein Kinase C
Protein Kinases
RNA
RNA Interference
Statistics as Topic
Ubiquitin-Protein Ligase Complexes
Protein Isoforms
Protein Kinase C
Protein Kinases
RNA
Ubiquitin-Protein Ligase Complexes
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