P-30: The Investigation of Transcript Expression Level of Mitochondrial Transcription Factor A (TFAM) during In Vitro Maturation (IVM) in Single Human Oocytes

Authors

  • A Allahveisi Infertility Center of Beassat Hospital, School of Medicine, Kurdistan University of Medical Sciences, Sanandaj, Iran
  • B Nikkhoo Department of Pathology, School of Medicine, Kurdistan University of Medical Sciences, Sanandaj, Iran
  • E Yosefian Department of Obstetrics and Gynecology, School of Medicine, Infertility Center of Shahid Beheshti University Hospital, Isfahan, Iran
  • MJ Rezaei Infertility Center of Beassat Hospital, School of Medicine, Kurdistan University of Medical Sciences, Sanandaj, Iran
Abstract:

Background In vitro maturation (IVM) of human oocytes has acquired increasing attention in infertility treatment with great promise. This technique is an alternative conventional in vitro fertilization-embryo transfer (IVF-ET), and can be reduced the side effects of gonadotropin stimulation such as ovarian hyperstimulation (OHSS). Oocyte maturation is a complex process including cytoplasmic and nuclear maturation which essential for the acquisition of oocyte competence. Mitochondria are the most predominant organelle in human oocytes.Mitochondria are maternally inherited organelles that supply ATP to the cell by oxidative phosphorylation. Mitochondria have their own genomes. Little is known about the transcript expression of mitochondrial related genomes during oocyte maturation. This study was to identify mitochondrial transcription factor A (TFAM) during IVM in single human oocytes. MaterialsAndMethods Oocytes at various stages of germinal vesicle(GV) and metaphase I (MI) maturation obtained from 27 consenting women (age 21–35 years), with male factors who were selected for ovarian stimulation and ICSI procedures. Matured oocytes (MII) were generated following IVM. The mRNA level of TFAM identified using single cell taqman Real time-PCR. Results The expression level of the target TFAM gene was low at the germinal vesicle (GV) and MI stages (P>0.05). Although, the mRNA level of TFAM gene remained stable in metaphase II (MII) following IVM, the mRNA level of TFAM increased significantly at the stage of MII in in vivo (P

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Journal title

volume 9  issue 2

pages  56- 56

publication date 2015-09-01

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