Relationship between Microdeletions on the Y Chromosome and Defect of Spermatogenesis

Y 염색체 미세결실과 정자형성장애의 연관성에 대한 연구

  • Lee, Hyoung-Song (Laboratory of Reproductive Biology & Infertility, Samsung Cheil Hospital and Women's Healthcare Center, Sungkyunkwan University School of Medicine) ;
  • Choi, Hye-Won (Laboratory of Reproductive Biology & Infertility, Samsung Cheil Hospital and Women's Healthcare Center, Sungkyunkwan University School of Medicine) ;
  • Park, Yong-Seog (Laboratory of Reproductive Biology & Infertility, Samsung Cheil Hospital and Women's Healthcare Center, Sungkyunkwan University School of Medicine) ;
  • Koong, Mi-Kyoung (Department of Obstetrics and Gynecology, Samsung Cheil Hospital and Women's Healthcare Center, Sungkyunkwan University School of Medicine) ;
  • Kang, Inn-Soo (Department of Obstetrics and Gynecology, Samsung Cheil Hospital and Women's Healthcare Center, Sungkyunkwan University School of Medicine) ;
  • Yun, Jong-Min (Department of Urology, Samsung Cheil Hospital and Women's Healthcare Center, Sungkyunkwan University School of Medicine) ;
  • Lee, You-Sik (Department of Urology, Samsung Cheil Hospital and Women's Healthcare Center, Sungkyunkwan University School of Medicine) ;
  • Seo, Ju-Tae (Department of Urology, Samsung Cheil Hospital and Women's Healthcare Center, Sungkyunkwan University School of Medicine) ;
  • Jun, Jin-Hyun (Laboratory of Reproductive Biology & Infertility, Samsung Cheil Hospital and Women's Healthcare Center, Sungkyunkwan University School of Medicine)
  • 이형송 (삼성제일병원 생식생물학 및 불임연구실) ;
  • 최혜원 (삼성제일병원 생식생물학 및 불임연구실) ;
  • 박용석 (삼성제일병원 생식생물학 및 불임연구실) ;
  • 궁미경 (성균관대학교 의과대학 산부인과학교실) ;
  • 강인수 (성균관대학교 의과대학 산부인과학교실) ;
  • 윤종민 (성균관대학교 의과대학 비뇨기과학교실) ;
  • 이유식 (성균관대학교 의과대학 비뇨기과학교실) ;
  • 서주태 (성균관대학교 의과대학 비뇨기과학교실) ;
  • 전진현 (삼성제일병원 생식생물학 및 불임연구실)
  • Published : 2002.12.30

Abstract

Objective s: To estimate the frequency of Y chromosome microdeletions in the Korean population of infertile men and to evaluate the relationship between microdeletion on the Y chromosome and clinical phenotypes of infertile men with idiopathic azoospermia and oligozoospermia. Materials and Methods: Genomic DNA was extracted from blood samples collected from 330 infertile men attending the Infertility Clinic at Samsung Cheil Hospital, Korea. Six sequence tagged sites (STSs) spanning the azoospermia factor (AZF) regions of the Y chromosome were amplified by polymerase chain reactions (PCRs). Results: Microdeletions on Y chromosome were detected in 35 (10.6%) of the 330 infertile men. Most of the microdeletions (91.4%) involved AZFb or AZFc. The high incidence of microdeletions were found in AZFc region (57.1%), but the low in AZFa (8.6%) and AZFb (5.7%). Larger microdeletions involving two or three AZF regions were detected in 28.6% of cases. All patients (6 patients) with deletion of AZFa region showed no germ cell phenotypes, Sertoli cell only syndrome or Leydig cell hyperplasia in histopathologic examinations. Conclusion: Microdeletions on the Y chromosome, especially, at AZFc/DAZ regions may be the major cause of azoospermia and severe oligozoospermia. We suggest that idiopathic infertile men have genetic counselling and microdeletion analysis on the Y chromosome before IVF-ET and ART program.

Keywords

References

  1. Ma K, Sharkey A, Kirsch S, Vogt P, Keil R, Hargreave TB, et al. Towards the molecular localisation of the AZF locus: mapping of microdeletions in Azoospermic men within 14 subintervals of interval 6 of the human Y chromosome. Hum Mol Genet 1992; 1: 29-33 https://doi.org/10.1093/hmg/1.1.29
  2. Reijo R, Alagappan RK, Patrizio P, Page DC. Severe oligozoospermia resulting from deletions of azoospermia factor gene on Y chromosome. Lancet 1996; 347: 1290-3 https://doi.org/10.1016/S0140-6736(96)90938-1
  3. Vogt PH, Edelmann A, Kirsch S, Henegariu O, Hirschmann P, Kiesewetter F, et al. Human Y chromosome azoospermia factor (AZF) mapped to different subregions in Yq11. Hum Mol Genet 1996; 5: 933-43 https://doi.org/10.1093/hmg/5.7.933
  4. Lee HJ, Lee HS, Song GJ, Byun HK, Seo IT, Kim JH, et al. Analysis of the Azoospermia Factor (AZF) gene on Y chromosome and expression pattem of DAZ gene in Korean infertile men. Kor J Fertil Steril 1997; 24: 57-66
  5. van der Ven K, Montag M, Peschka B, Leygraaf J, Schwanitz G, Haidl G, et aI. Combined cytogenetic and Y chromosome microdeletion screening in males undergoing intracytoplasmic sperm injection. Mol Hum Reprod 1997; 3: 699-704 https://doi.org/10.1093/molehr/3.8.699
  6. Foresta C, Ferlin A, Garolla A, Moro E, Pistorello M, Barbaux S, et al. High frequency of well-defined V-chromosome deletions in idiopathic Sertoli cell-only syndrome. Hum Reprod 1998; 13: 302-7 https://doi.org/10.1093/humrep/13.2.302
  7. Peterlin B, Kunej T, Sinkovec J, Gligorievska N, Zorn B. Screening for Y chromosome microdeletions in 226 Siovenian subfertile men. Hum Reprod 2002; 17: 17-24
  8. Tiepolo L, Zuffardi O. Localization of factors controlling spermatogenesis in the nonfluorescent of the human Y chromosome long arm. Hum Genet 1976; 34: 119-24 https://doi.org/10.1007/BF00278879
  9. Ma K, Inglis JD, Sharkey A, Bickmore WA, Hill RE, Prosser EJ, et al. A Y Chromosome Gene Family with RNA-Binding Protein Homology: Candidates for the Azoospermia Factor AZF Controlling Human Spermatogenesis. Cell 1993; 75: 1287-95 https://doi.org/10.1016/0092-8674(93)90616-X
  10. Reijo R, Lee TY, Salo P, Alagappan R, Brown LG, Rosenberg S, et al. Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene. Nature Genetics 1995; 10: 383-93 https://doi.org/10.1038/ng0895-383
  11. Silber SJ, Alagappan R, Brown LG, Page DC. Y chromosome deletions in azoospermic and severely oligozoospermic men undergoing intracytoplasmic sperm injection after testicular sperm extraction. Hum Reprod 1998; 13: 3332-7 https://doi.org/10.1093/humrep/13.12.3332
  12. Stuppia L, Gatta V, Calabrese G, Guanciali FP, Morizio E, Bombieri C, et aI. A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11. Hum Genet 1998; 102: 566-70 https://doi.org/10.1007/s004390050741
  13. Page DC, Silber S, Brown LG. Men with infertility caused by AZFc deletion can produce sons by intracytoplasmic sperm injection, but are likely to transmit the deletion and infertility. Hum Reprod 1999; 14: 1722-6 https://doi.org/10.1093/humrep/14.7.1722
  14. Vollrath D, Foote S, Hilton A, Brown LG, BeerRomero P, Bogan JS, et al. The human Y chromosome: A 43-interval map based on naturally occurring deletions. Science 1992; 258: 52-9 https://doi.org/10.1126/science.1439769
  15. Simoni M, Kamischke A, Nieschlag E. Current status of the molecular diagnosis of the Y-chromosomal microdeletions in the work-up of male infertility. Hum Reprod 1998; 13: 1764-8 https://doi.org/10.1093/humrep/13.7.1764
  16. Liow SL, Ghadessy FJ, Ng SC, Yong EL. Y chromosome microdeletions, in azoospermic or nearazoospermic subjecttts, are located in the AZFc (DAZ) subregion. Mol Hum Reprod 1998; 4: 763-8 https://doi.org/10.1093/molehr/4.8.763
  17. Chang SY, Tsai MY. Detection of azoospermic factor genes in Chinese men with azoospermia or severe oligospermia. J Assist Reprod Genet 1999;16: 259-62 https://doi.org/10.1023/A:1020367513161
  18. Chiang HS, Wei HJ, Chen YT. Genetic screening for patients with azoospermia and severe oligoasthenospermia. lnt J Androl 2000; 23 (Suppl 2): 20-5
  19. Tse JYM, Yeung WSB, Ng EHY, Cheng LN, Zhu HB, Teng XM, et aI. A comparative study of Y chromosome microdeletions in infertile males from two chinese populations. J Assist Reprod Genet 2002; 19: 376-83 https://doi.org/10.1023/A:1016346421177