Homozygous Splice Site Mutation in Causes Familial Oocyte Maturation Defect.
Fiche publication
Date publication
avril 2020
Journal
Genes
Auteurs
Membres identifiés du Cancéropôle Est :
Pr VIVILLE Stéphane, Dr CHARLET BERGUERAND Nicolas
Tous les auteurs :
Okutman Ö, Demirel C, Tülek F, Pfister V, Büyük U, Muller J, Charlet-Berguerand N, Viville S
Lien Pubmed
Résumé
In vitro fertilization (IVF) involves controlled ovarian hyperstimulation using hormones to produce large numbers of oocytes. The success of IVF is tightly linked to the availability of mature oocytes. In most cases, about 70% to 80% of the oocytes are mature at the time of retrieval, however, in rare instances, all of them may be immature, implying that they were not able to reach the metaphase II (MII) stage. The failure to obtain any mature oocytes, despite a well conducted ovarian stimulation in repeated cycles is a very rare cause of primary female infertility, for which the underlying suspected genetic factors are still largely unknown. In this study, we present the whole exome sequencing analysis of a consanguineous Turkish family comprising three sisters with a recurrent oocyte maturation defect. Analysis of the data reveals a homozygous splice site mutation (c.1775-3C>A) in the zona pellucida glycoprotein 1 () gene. Minigene experiments show that the mutation causes the retention of the intron 11 sequence between exon 11 and exon 12, resulting in a frameshift and the likely production of a truncated protein.
Mots clés
female infertility, immature oocytes, oocyte maturation defect
Référence
Genes (Basel). 2020 Apr 1;11(4):