Article Text

PDF
Identification of a 2244 base pair interstitial deletion within the human ESR1 gene in the Spanish population
  1. J Jorge Galan1,
  2. B Buch2,
  3. S Pedrinaci3,
  4. P Jimenez-Gamiz3,
  5. A Gonzalez4,
  6. M Serrano-Rios5,
  7. A Salinas1,
  8. M del Carmen Rivero1,
  9. L M Real1,
  10. J L Royo1,
  11. A Ruiz1
  1. 1
    Department of Structural Genomics, Neocodex SL, Seville, Spain
  2. 2
    Unidad de Reproduccion, Centro Gutenberg, Malaga, Spain
  3. 3
    Servicio de Analisis Clinicos, Hospital Universitario Virgen de las Nieves, Granada, Spain
  4. 4
    Centro Avanzado de Fertilidad (CAF), Jerez, Cadiz, Spain
  5. 5
    Hospital Clinico Universitario San Carlos, Madrid, Spain
  1. Dr J J Galan, Neocodex SL, Department of Structural Genomics, Avda, Charles Darwin 6, Acc. A, Isla de la Cartuja, 41092 Seville, Spain; jjgalan{at}neocodex.es

Abstract

Background: The ESR1 AGATA haplotype is composed of five markers located within introns 5 and 6 of the human oestrogen receptor 1 (ESR1) gene. This haplotype has been studied in several male urogenital tract anomalies and male infertility. In one of these studies, a deviation from Hardy–Weinberg equilibrium (DHW) was found for the ESR1 AGATA marker rs3020375 in two groups of healthy controls. In the present study, we investigated whether the observed DHW is caused by structural variants present within the ESR1 gene.

Participants: 229 family units achieving pregnancy through assisted reproductive technologies (n = 129) or by natural means (n = 100), 2465 general Spanish population controls and 162 men with idiopathic infertility.

Main outcome measurements: Segregation analyses of genetic markers in family units and case–control genetic association studies.

Results: We identified a new interstitial deletion of 2244 base pairs within intron 6 of the human ESR1 gene as the cause for the observed DHW. This new variant presents a 10% allelic frequency in the general Spanish population and it is associated with idiopathic male infertility (OR = 1.51; p = 0.03). The percentage of infertile couples in which both members carried the ESR1 deletion (10.08%) was also a higher than expected value of 6% (p = 0.03).

Conclusions: We have characterised a novel structural variation in human ESR1 gene. The available data indicate a deleterious action of the ESR1 deletion in both male and couple fertility. The potential effects of this deletion on other oestrogen-related diseases need to be determined.

Statistics from Altmetric.com

Footnotes

  • Funding: This study has been funded by the European Commission 5th Framewok Programme (QLTR-2001-02403), the Ministerio de Educacion y Ciencia of Spain (CIT-090100-2007-57 and PTQ04-1-0006) and the Fundacion OSKAR.

  • Competing interests: None.

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.