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Molecular Human Reproduction, Vol. 7, No. 5, 425-429, May 2001
© 2001 European Society of Human Reproduction and Embryology


Embryology

Mitochondrial DNA content affects the fertilizability of human oocytes

P. Reynier1,4, P. May-Panloup2, M-F. Chrétien2, C.J. Morgan1, M. Jean3, F. Savagner1, P. Barrière3 and Y. Malthièry1

1 INSERM EMI-U 00-18, Laboratoire de Biochimie et Biologie Moléculaire, CHU d'Angers, F-49033 Angers, 2 Laboratoire d'Histologie-Embryologie-Cytologie et Laboratoire de FIV, CHU d'Angers, F-49033 Angers and 3 Biologie de la Reproduction, Pavillon de la Mère et de l'Enfant, CHU de Nantes, B.P. 1005, F-44093 Nantes cedex 1, France

Abstract

Mitochondrial DNA content varies considerably in oocytes, even when collected from the same patient. In the present study, real-time quantitative polymerase chain reaction analysis of 113 unfertilized oocytes obtained from 43 patients revealed an average of 193 000 (range: 20 000 to 598 000) mitochondrial genomes per cell. We compared several groups of oocytes to investigate the relationship between mitochondrial DNA content and fertilizability. The average mitochondrial DNA copy number was significantly lower in cohorts suffering from fertilization failure compared to cohorts with a normal rate of fertilization. In addition, the mitochondrial copy number of oocytes from patients with fertilization failure due to unknown causes was significantly lower than that of oocytes from patients in which IVF failure was due mainly to a severe sperm defect. The lower mtDNA copy number could be due to defective cytoplasmic maturation of oocytes. We conclude that low mitochondrial DNA content, due to inadequate mitochondrial biogenesis or cytoplasmic maturation, may adversely affect oocyte fertilizability.

cytoplasmic maturation/mitochondrial biogenesis/mtDNA/oocyte/real-time PCR

Notes

4 To whom correspondence should be addressed. E-mail: pareynier{at}chu-angers.fr


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