Incidence of diploid and disomic sperm nuclei in 45 infertile men

Human Reproduction

Volumn 12, Issue 3, 1997, Pages 468-473

  Guttenbach, M ^a   Martinez Exposito M J ^a   Michelmann, H W ^b   Engel, W ^c   Schmid, M ^a  

^a UNIVERSITY OF WÜRZBURG   (Germany)

^b Dept of Obstetrics and Gynecology ^*  (Germany)

^c UNIVERSITY OF GÖTTINGEN   (Germany)

Author keywords

Diploidy; Disomy; Human spermatozoa; In situ hybridization; Infertility

Indexed keywords

ADULT; ARTICLE; ASTHENOSPERMIA; CHROMOSOME 1; CHROMOSOME 10; CHROMOSOME 17; CHROMOSOME 7; CLINICAL ARTICLE; CONTROLLED STUDY; DIPLOIDY; DISOMY; HUMAN; HUMAN CELL; INCIDENCE; MALE; MALE INFERTILITY; OLIGOSPERMIA; SPERM; SPERMATOZOON; X CHROMOSOME; Y CHROMOSOME;

EID: 1842298135     PISSN: 02681161     EISSN: None     Source Type: Journal    
DOI: 10.1093/humrep/12.3.468     Document Type: Article

References (35)

1. Bischoff, F.Z., Nguyen, D.D., Burt, K.J. and Shaffer, L.G. (1994) Estimates of aneuploidy using multicolor fluorescence in situ hybridization on human sperm. Cytogenet. Cell Genet., 66, 237-243.
2. Brandriff, B., Gordon, L., Ashworth, L. et al. (1985) Chromosomes of human sperm: variability among normal individuals. Hum. Genet., 70, 18-24.
3. Carothers, A.D. and Beatty, R.A. (1975) The recognition and incidence of haploid and polyploid spermatozoa in man, rabbit and mouse. J. Reprod. Fertil., 44, 487-500.
4. Chevret, E., Rousseaux, S., Monteil, M. et al. (1995) Meiotic segregation of the X and Y chromosomes and chromosome 1 analyzed by three-color FISH in human interphase spermatozoa. Cytogenet. Cell Genet., 71, 126-130.
5. Cooke, H. (1976) Repeated sequence specific to human males. Nature, 262, 182-186.
6. Cooke, H.J. and Hindley, J. (1979) Cloning of human satellite III DNA: different components are on different chromosomes. Nucleic Acids Res., 6, 3177-3197.
7. Goldman, A.S.H., Fomina, Z., Knights, P.A. et al. (1993) Analysis of the primary sex ratio, sex chromosome aneuploidy and diploidy in human sperm using dual-colour fluorescence in situ hybridization. Ear. J. Hum. Genet., 1, 325-334.
8. Griffin, D.K., Abruzzo, M.A., Millie, E.A. et al. (1995) Nondisjunction in human sperm: evidence for an effect of increasing paternal age. Hum. Mol. Genet., 4, 2227-2232.
9. Guttenbach, M. and Schmid, M. (1990) Determination of Y chromosome aneuploidy in human sperm nuclei by nonradioactive in situ hybridization. Am. J. Hum. Genet., 46, 553-558.
10. Guttenbach, M. and Schmid, M. (1991) Non-isotopic detection of chromosome 1 in human meiosis and demonstration of disomic sperm nuclei. Hum. Genet., 87, 261-265.
11. Guttenbach, M., Schakowski, R. and Schmid, M. (1994a) Incidence of chromosome 3, 7, 10, 11, 17 and X disomy in mature human sperm nuclei as determined by nonradioactive in situ hybridization. Hum. Genet., 93, 7-12.
12. Guttenbach, M., Schakowski, R. and Schmid, M. (1994b) Incidence of chromosome 18 disomy in human sperm nuclei as detected by nonisotopic in situ hybridization. Hum. Genet., 93, 421-423.
13. Han, T.L., Webb, G.C., Flaherty, S.P. et al. (1992) Detection of chromosome 17- and X-bearing human spermatozoa using fluorescence in situ hybridization. Mol. Reprod. Dev., 33, 189-194.
14. Han, T.L., Ford, J.H., Webb, G.C. et al. (1993) Simultaneous detection of X- and Y-bearing human sperm by double fluorescence in situ hybridization. Mol. Reprod. Dev., 34, 308-313.
15. Hargreave, T.B. (1990) Introduction. In Hargreave, T.B. and Soon, T.E. (eds), The Management of Male Infertility. PG Publishing, Singapore, pp. 2-21.
16. Hinney, B., Wilke, G. and Michelmann, H.W. (1993) Prognostic value of an automated sperm analysis in IVF or insemination therapy. Andrologia, 25, 195-202.
17. Holmes, J.M. and Martin, R.H. (1993) Aneuploidy detection in human sperm nuclei using fluorescence in situ hybridization. Hum. Genet., 91, 20-24.
18. Jackson-Cook, C. and Haller, V.L. (1991) Estimation of aneuploidy levels in human spermatozoa using chromosome complements and chromosome specific probes. Am. J. Hum. Genet., 49 (Suppl. A), 18.
19. Lu, P. Y., Hammit, D.G., Zinsmeister, A.R. and Dewald, G.W. (1994) Dual color fluorescence in situ hybridization to investigate aneuploidy in sperm from 33 normal males and a man with a t(2;4;8)(q23;q27;p21). Fertil Steril., 62, 394-399.
20. Martin, R.H. and Rademaker, A. (1990) The frequency of aneuploidy among individual chromosomes in 6,821 human sperm chromosome complements. Cytogenet. Cell Genet., 53, 103-107.
21. Martin, R.H. and Rademaker, A. (1995) Reliability of aneuploidy estimates in human sperm: results of fluorescence in situ hybridization studies using two different scoring criteria. Mol. Reprod. Dev., 42, 89-93.
22. Martin, R.H., Ko, E. and Chan, K. (1993) Detection of aneuploidy in human interphase spermatozoa by fluorescence in situ hybridization (FISH). Cytogenet. Cell Genet., 64, 23-26.
23. Michelmann, H.W. (1995) Minimal criteria of sperm quality for insemination and IVF therapy. Int. J. Androl., 18 (Suppl. 2), 81-87.
24. Miharu, N., Best, R.G. and Young, S.R. (1994) Numerical chromosome abnormalities in spermatozoa of fertile and infertile men detected by fluorescence in situ hybridization. Hum. Genet., 93, 502-506.
25. Moosani, N., Pattinson, H.A., Carter, M.D. et al. (1995) Chromosomal analysis of sperm from men with idiopathic infertility using karyotyping and fluorescence in situ hybridization. Fertil. Steril., 64, 811-817.
26. Pieters, M.H.E.C., Geraedts, J.P.M., Meyer, H. et al. (1990) Human gametes and zygotes studied by nonradioactive in situ hybridization. Cytogenet. Cell Genet., 53, 15-19.
27. Robbins, W.A., Segraves, R., Pinkel, D. and Wyrobek, A.J. (1993) Detection of aneuploid human sperm by fluorescence in situ hybridization: evidence for a donor difference in frequency of sperm disomic for chromosomes 1 and Y. Am. J. Hum. Genet., 52, 799-807.
28. Rudak, E., Jacobs, P.A. and Yanagimachi, R. (1978) Direct analysis of the chromosome constitution of human spermatozoa. Nature, 274, 911-913.
29. Sara, A. (1987) Epidemiology of human reproduction. In Advances in Fertility and Sterility. Proc. 12th World Congress Fertil. Steril., 4, 91-91.
30. Spriggs, E.L., Rademaker, A.W. and Martin, R.H. (1995) Aneuploidy in human sperm: results of two- and three-color fluorescence in situ hybridization using centromeric probes for chromosomes 1, 12, 15, 18, X, and Y. Cytogenet. Cell Genet., 71, 47-53.
31. World Health Organization (1992) WHO Laboratory Manual for the Examination of Human Semen and Sperm-Cervical Mucus Interaction, 3rd edn. Springer Verlag, Berlin.
32. Willard, H.F., Smith, K.D. and Sutherland, J. (1983) Isolation and characterization of a major tandem repeat family from the human X chromosome. Nucleic Acids Res., 11, 2017-2033.
33. Williams, B.J., Ballenger, C.A., Malter, H.E. et al. (1993) Non-disjunction in human sperm: results of fluorescence in situ hybridization studies using two and three probes. Hum. Mol. Genet., 2, 1929-1936.
34. Wyrobek, A.J., Robbins, W.A., Mehraein, Y. et al. (1994) Detection of sex chromosomal aneuploidies X-X, Y-Y, and X-Y in human sperm using two-chromosome fluorescence in situ hybridization. Am. J. Med. Genet., 53, 1-7.
35. Yang, T.P., Hansen, S.K., Oishi, K.K., et al. (1982) Characterization of a cloned repetitive DNA sequence concentrated on the human X chromosome. Proc. Natl. Acad. Sci. USA, 79, 6593-6597.