Clin Exp Reprod Med.  2012 Jun;39(2):58-67. 10.5653/cerm.2012.39.2.58.

Function of the pentose phosphate pathway and its key enzyme, transketolase, in the regulation of the meiotic cell cycle in oocytes

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

Abstract


OBJECTIVE
Previously, we identified that transketolase (Tkt), an important enzyme in the pentose phosphate pathway, is highly expressed at 2 hours of spontaneous maturation in oocytes. Therefore, this study was performed to determine the function of Tkt in meiotic cell cycle regulation, especially at the point of germinal vesicle breakdown (GVBD).
METHODS
We evaluated the loss-of-function of Tkt by microinjecting Tkt double-stranded RNAs (dsRNAs) into germinal vesicle-stage oocytes, and the oocytes were cultured in vitro to evaluate phenotypic changes during oocyte maturation. In addition to maturation rates, meiotic spindle and chromosome rearrangements, and changes in expression of other enzymes in the pentose phosphate pathway were determined after Tkt RNA interference (RNAi).
RESULTS
Despite the complete and specific knockdown of Tkt expression, GVBD occurred and meiosis was arrested at the metaphase I (MI) stage. The arrested oocytes exhibited spindle loss, chromosomal aggregation, and declined maturation promoting factor and mitogen-activated protein kinase activities. The modified expression of two enzymes in the pentose phosphate pathway, Prps1 and Rbks, after Tkt RNAi and decreased maturation rates were amended when ribose-5-phosphate was supplemented in the culture medium, suggesting that the Tkt and pentose phosphate pathway are important for the maturation process.
CONCLUSION
We concluded that Tkt and its associated pentose phosphate pathway play an important role in the MI-MII transition of the oocytes' meiotic cell cycle, but not in the process of GVBD.

Keyword

Oocyte; Meiosis; RNA interference; Transketolase; Pentose phosphate pathway

MeSH Terms

Cell Cycle
Maturation-Promoting Factor
Meiosis
Metaphase
Oocytes
Pentose Phosphate Pathway
Protein Kinases
Ribosemonophosphates
RNA Interference
RNA, Double-Stranded
Transketolase
Maturation-Promoting Factor
Protein Kinases
RNA, Double-Stranded
Ribosemonophosphates
Transketolase
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