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BMC Genomics

Open Access

Linkage analysis coupled with exome sequencing identified defects in gene ‘X’ causing premature ovarian insufficiency

BMC Genomics201415(Suppl 2):P6

https://doi.org/10.1186/1471-2164-15-S2-P6

Published: 2 April 2014

Background

Premature ovarian insufficiency (POI) is defined as a primary ovarian defect characterized by absent menarche (primary amenorrhea) or premature depletion of ovarian follicles before the age of 40 (secondary amenorrhea) with hypergonadotropism and hypoestrogenism. POI results in infertility and lifelong steroid deficiency, and is potentially associated with accelerated health risks such as cardiovascular and neurodegenerative disorders and osteoporosis.

Materials and methods

A large consanguineous Saudi family with three female affected with POI was investigated. All samples including 3 affected and 6 unaffected underwent whole genome SNP genotyping using Affymetric 250K array. Linkage analysis was carried out using HomozygosityMapper and Allegro software. Candidate gene sequencing was performed using ABI3500 genetic analyzer. Whole exome was sequenced in three affected and one normal individual using life technologies Ion Proton sequencer.

Results

Linkage analysis mapped the disease phenotype to long arm of chromosome 20. Sequence data analysis of potential candidate genes failed to detect any pathogenic variant. Exome sequencing data analysis identified a deletion mutation in gene ‘X’ on long arm of chromosome 20. This mutation is perfectly segregating with the disease phenotype in pedigree.

Conclusions

We identified a novel gene responsible for POI in Saudi Arabian family. Our findings extend the body of evidence that supports the importance of gene ‘X’ in the development of ovary and ovarian reserves.

Authors’ Affiliations

(1)
Center for Genetics and Inherited Diseases, Taibah University Madinah Al-Munawara

References

  1. Wu X, Wang B, Dong Z, Zhou S, Liu Z, Shi G, Cao Y, Xu Y: A NANOS3 mutation linked to protein degradation causes premature ovarian insufficiency. Cell Death Dis. 2013, 4: e825-PubMed CentralView ArticlePubMedGoogle Scholar
  2. Wang H, Sun M, Qin Y, Xia T, Ma J, Chen ZJ: Mutations in DMC1 are not responsible for premature ovarian failure in Chinese women. Reprod Biomed Online. 2013, 26 (2): 175-8.View ArticlePubMedGoogle Scholar

Copyright

© Basit; licensee BioMed Central Ltd. 2014

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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