Background:
Newborn ovary homeobox (
NOBOX
) gene plays a critical role in the transcriptional regulation of oocyte-specific genes. Previous studies have demonstrated a pathogenic effect of
NOBOX
variants on premature ovarian insufficiency (POI) patients. Poor ovarian response (POR) is a risk factor for POI. Therefore, genetic variants in the
NOBOX
gene may also be studied as risk factors for POR development.
Aims:
The aim of the study is to investigate the association between seven known
NOBOX
single-nucleotide polymorphisms (SNPs) and POR in Jordanian females.
Settings and Design:
This was a case–control study of 60 females with POR for controlled ovarian hyperstimulation and 59 healthy females with no history of reproductive problems. Blood samples were collected from the participants and seven SNPs of
NOBOX
gene were screened.
Subjects and Methods:
DNA was extracted from blood samples. Polymerase chain reaction with primers specific for seven known SNPs in
NOBOX
gene was used to amplify the specified region within the gene followed by Sanger sequencing.
Results:
The seven SNPs investigated in this study, namely, rs77587352 (c.271G>T, p. Gly91Trp), rs7800847 (c.349C>T, p. Arg117Trp), rs193303102 (c.907C>T, p. Arg303X), rs193303103 (c.1025G>C, p. Ser342Thr), rs193303104 (c.1048G>T, p. Val350Leu), rs201947677 (c.1064G>A, p. Arg355His), and rs146227301 (c.1856C>T, p. Pro619Leu), only represent the wild-type allele in both females with POR and healthy participants.
Conclusions:
The results show that only monomorphic genotype of the
NOBOX
variants was found in Jordanian females studied.