Sex chromosomal analysis of spermatozoa from infertile men using fluorescence in situ hybridization

Journal of Assisted Reproduction and Genetics

Volumn 17, Issue 2, 2000, Pages 97-102

  Nishikawa, Naomi ^a   Murakami, Isamu ^a   Ikuta, Katsuo ^a   Suzumori, Kaoru ^a  

^a NAGOYA CITY UNIV MEDICAL SCHOOL   (Japan)

Author keywords

FISH; Infertile men; Sex chromosome aneuploidy; Spermatozoa; XY disomy

Indexed keywords

ANEUPLOIDY; CHROMOSOME 18; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CONFERENCE PAPER; CONTROLLED STUDY; DISEASE ASSOCIATION; DISOMY; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC RISK; HUMAN; HUMAN CELL; MALE INFERTILITY; PRIORITY JOURNAL; REPRODUCTION; SEX CHROMOSOME; SPERMATOZOON;

ANEUPLOIDY; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 18; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; OLIGOSPERMIA; SEX CHROMOSOMES; SPERMATOZOA;

EID: 0033995862     PISSN: 10580468     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1009413916753     Document Type: Article

References (34)

1. Palermo GD, Colombero LT, Schattman GL, Davis OK, Rosenwaks Z: Evolution of pregnancies and initial follow-up of newborns delivered after intracytoplasmic sperm injection. JAMA 1996;276:1893-1897
2. Liebaers I, Bonduelle M, Assche E, Derroey P, Steirteghem A: Sex chromosome abnormalities after intracytoplasmic sperm injection. Lancet 1995;346:1095
3. In't Veld P, Brandenburg H, Verhoeff A, Dhout M, Los F: Sex chromosome abnormalities and intracytoplasmic sperm injection. Lancet 1995;346:773
4. Bonduelle M, Legein J, Derde MP, Buysse A, Schietecatte J, Wisanto A, Derroey P: Comparative follow-up study of 130 children born after intracytoplasmic sperm injection and 130 children born after in-vitro fertilization. Hum Reprod 1995;12:3327-3331
5. Rudak E, Jacobs PA, Yanagimachi R: Direct analysis of the chromosome constitution of human spermatozoa. Nature 1978;274:911-913
6. Martin R.H: A detailed method for obtaining preparations of human sperm chromosomes. Cytogenet Cell Genet 1983;35:253-256
7. Guttenbach M, Engel W, Schmid M: Analysis of structural and numerical chromosome abnormalities in sperm of normal men and carriers of constitutional chromosome aberrations. A review. Hum Genet 1997;100:1-21
8. Holmes JM, Martin RH: Aneuploidy detection in human sperm nuclei using fluorescence in situ hybridization. Hum Genet 1993;91:20-24
9. Spriggs EL, Rademaker AW, Martin RH: Aneuploidy in human sperm: The use of multicolor FISH to test various theories of nondisjunction. Am J Hum Genet 1996;58:356-362
10. Robbins WA, Segraves R, Pinkel D, Wyrobek AJ: 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 1993;52:799-807
11. rd ed. Berlin, Springer, Verlag, 1992
12. Vidal F, Moragas M, Catala V, Torelló MJ, Santaló J, Calderóu G, Gimenez C, Barri PN, Egozcue J, Veiga A: Sephadex filtration and human serum albumin gradients do not select spermatozoa by sex chromosome: A fluorescent in-situ hybridization study. Hum Reprod 1993,8:1740-1743
13. Blanco J, Egozcue J, Vidal F: Incidence of chromosome 21 disomy in human spermatozoa as determined by fluorescent in-situ hybridization. Hum Reprod 1996;11:722-726
14. Williams BJ, Ballenger CA, Malter HE: Non-disjunction in human sperm: results of fluorescence in situ hybridization studies using two and three probes. Hum Mol Genet 1993;2:929-1936
15. Miharu N, Best R, Young S: Numerical chromosome abnormalities in spermatozoa of fertile and infertile men detected by fluorescence in situ hybridization. Hum Genet 1994;93:502-506
16. Guttenbach M, Martinez-Expóstio M-J, Michelmann HW, Engel M, Schmid M: Incidence of diploid and disomic sperm nuclei in 45 infertile men. Hum Reprod 1997;12:468-473
17. Lähdetie J, Saari N, Ajosenpää-Saari M, Mykkänen J: Incidence of aneuploid spermatozoa among infertile men studied by multicolor fluorescence in situ hybridization. Am J Med Genet 1997;71:115-121
18. Pang MG, Zackowski JL, Hoegerman SF, Moon SY, Cuticchia AJ, Acosta AA, Kearns WG: Detection by fluorescence in situ hybridization of chromosome 7, 11, 12, 18, X and Y abnormalities in sperm from oligoasthenospermic patients of an in vitro fertilization program. J Assist Reprod Genet 1995; 12 (Suppl):53S
19. Pang MG, Hoegerman SF, Cuticchia AJ, Moon SY, Doncel GF, Acosta AA, Kearns WG: Detection of aneuploidy for chromosomes 4, 6, 7, 8, 9, 10, 11, 12, 13, 17, 18, 21, X and Y by fluorescence in-situ hybridization in spermatozoa from nine patients with oligoasthenoteratozoospermia undergoing intracytoplasmic sperm injection. Human Reprod 1999; 14:1266-1273
20. Moosani N, Pattinson HA, Carter MD, Cox DM, Rademaker AW, Martin RH: Chromosoma analysis of sperm from men with idiopathic infertility using sperm karyotyping in situ hybridization. Fertil Steril 1995;64:811-817
21. Martin RH: Genetics of human sperm. J Assist Reprod Genet 1998;15:240-245
22. Egozcue J, Templado C, Vidal F, Navarro J, Morer-Fargas F, Marina S: Meiotic studies in a series of 1100 infertile and sterile males. Hum Genet 1983;65:185-188
23. Guttenbach M, Michelmann HW, Hinney B, Engel W, Schmid M: Segregation of sex chromosomes into sperm nuclei in a man with 47,XXY Klinefelter's karyotype: A FISH analysis. Hum Genet 1997;99:474-477
24. Chevret E, Rousseaux S, Monteil M, Usson Y, Cozzi J, Pelletier R, Sele B : Increased incidence of hyperhaploid 24,XY spermatozoa detected by three-colour FISH in a 46,XY/47,XYY male. Hum Genet 1996;67:171-175
25. Cozzi J, Chevret E, Rousseaux S, Pelletier R, Benitz V, Jalbert H, Sele B: Achievement of meiosis in XXY germ cells: study of 543 sperm karyotypes from an XY/XXY mosaic patient. Hum Genet 1994;93:32-34
26. Roland K, Guttenbach M, Bettina S, Schubert R, Ven H, Schmid M, Propping P: Genetic counseling in a patient with XXY/ XXXY/XY mosaic Klinefelter's syndrome: estimate of sex chromosome aberrations in sperm before intracytoplasmic sperm injection. Fertil Steril 1998;69:482-485
27. Wyrobek AJ, Robbins WA, Mehraein Y, Pinkel D, Weiter H-U: Detection of human sperm carrying sex chromosomal and autosomal aneuploidies using one, two and three-color fluorescence in situ hybridizations. Am J Hum Genet 1992;51:A23
28. Chevret E, Rousseaux S, Monteil M, Cozzi J, Pelletier R, Mollard J, Sele B: Male meiotic segregation of gonosomes analyzed by two-color FISH in human interphase spermatozoa. Hum Genet 1994;97:701-704
29. Guttenbach M, Schakowski R, Schmid M: Incidence of chromosome 18 disomy in human sperm nuclei as detected by nonisotopic in situ hybridization. Hum Genet 1994;93:421-423
30. Chevret E, Rousseaux S, Monteil M, Pelletier R, Cozzi J, Sele B: Meiotic segregation of the X and Y chromosomes and chromosomes 1 analyzed by three-color FISH in human interphase spermatozoa. Cytogenet Cell Genet 1995;71:126-130
31. Abruzzo MA, Griffin DK, Millie EA, Sheean LA, Hassold TJ: The effect of Y-chromosome alpha-satellite length on the rate of sex chromosome disomy in human sperm. Hum Genet 1996;97:819-823
32. Han TL, Ford JH, Webb GC, Flaherty SP, Correll A, Matthens CD: Simultaneous detection of X- and Y- bearing human sperm by double fluorescence in situ hybridization. Mol Reprod Dev 1993;34:308-313
33. Lu PY, Hammit DG, Zinsmeister AR, Dewald GW: 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 Stroll 1994;62:394-39933.
34. In't Veld P, Broekmans FJM, France HF, Pearson PL, Pieters MHEL, Kooiji RJ: Intracytoplasmic sperm injection (ICSI) and chromosomally abnormal spermatozoa. Hum Reprod 1997;12:752-754