Detection of aneuploidy in human spermatozoa using fluorescence in situ hybridization (FISH)

Japanese Journal of Human Genetics

Volumn 41, Issue 4, 1996, Pages 381-389

  Hu, He ^a   Miharu, Norio ^a   Mizunoe, Tomoya ^a   Nakaoka, Yoshiharu ^a   Okamoto, Etsuji ^a   Ohama, Koso ^a  

^a HIROSHIMA UNIV SCHOOL OF MEDICINE   (Japan)

Author keywords

aneuploidy; chromosome; fluorescence in situ hybridization; interphase; sperm

Indexed keywords

DNA;

ADULT; ANEUPLOIDY; ARTICLE; CHROMOSOME 1; CHROMOSOME 17; CHROMOSOME 18; DIPLOIDY; DISOMY; DNA PROBE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; MALE; SEMEN ANALYSIS; SPERMATOZOON; X CHROMOSOME; Y CHROMOSOME;

EID: 0030459048     PISSN: 09168478     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF01876328     Document Type: Article

References (26)

1. Balhorn R (1982): A model for the structure ofchromatin in mammalian sperm. J Cell Biol 93: 298-305
2. BischoflT FZ, Nguyen DD, Burt KJ, Schaffer LG (1994): Estimates of aneuploidy using multicolor fluorescence in situ hybridization on human sperm. Cytogenet Cell Genet 66: 237-243
3. Brandriff B, Cordon L, Ashworth L, Watchmaker G. Carrano A, Wyrobek A (1984): Chromosomal abnormalities in human sperm: comparisons among four healthy men. Hum Genet 66: 193-201
4. Brandriff B. Gordon L, Ashworth L, Watchmaker G, Moore D, Wyrobek A, Carrano A (1985): Chromosomes of human sperm: variability among normal individuals. Hum Genet 70: 18-24
5. Burns J, Chan VTM, Jonassan JA, Fleming KA, Taylor S, Mcgree JOD (1985): Sensitive system for visualizing biotinylated DNA probes hybridized in situ: Rapid sex determination of intact cells. J Clin Pathol 38: 1085-1092
6. Carothers AD, Beatty RA (1975): The recognition and incidence of haploid and polyploid spermatozoa in man, rabbit, and mouse. J Reprod Fertil 44: 487-500
7. Coonen E, Pieters MHEC, Dumoulin JCM, Meyer H, Evers JLH, Ramaekers FCS, Feraedis JPM (1991): Nonisotopic in situ hybridization as a method for nondisjunction studies in human spermatozoa. Mol Reprod Dev 28: 18-22
8. Griffin DK, Abruzzo MA, Millie EA, Sheean LA, Feingold E, Sherman SL, Hassold TJ (1995): Non-disjunction in human sperm: evidence for an effect of increasing paternal age. Hum Mol Genet 4: 2227-2232
9. Guttenbach M, Schmid M ( 1991 ): Non-isotopic detection of chromosome I in human meiosis and demonstration of disomic sperm nuclei. Hum Genet 87: 261-265
10. Guttenbach M, Schakowski R, Schmid M (1994a): Incidence of chromosome 3, 7, 10, 11, 17, and X disomy in mature human sperm nuclei as determined by non-radioactive in situ hybridization. Hum Genet 93: 7-12
11. Guttenbach M, Schakowski R, Schmid M ( 1994b): Incidence of chromosome 18 disomy in human sperm nuclei as detected by nonisotopic in situ hybridization. Hum Genet 93: 421-423
12. Han TL, Webb GC, Flaherty SP, Correll A. Matthews CD, Ford JH (1992): Detection of chromosome 17- and X-bearing human spermatozoa using fluorescence in situ hybridization. Mol Reprod Dev 33: 189-194
13. Hassold TJ, Sherman SL (1993): The origin of non-disjunction in humans. Vol 11. Cambridge Univ Press, Cambridge, pp 313-322
14. Holmes JM, Martin RH (1993): Aneuploidy detection in human sperm nuclei using fluorescence in situ hybridization. Hum Genet 91: 20-24
15. Joseph AM, Gosden JR. Chandley AC (1984): Estimation of aneuploidy levels in human spermatozoa using chromosome specific probes and in situ hybridization. Hum Genet 66: 234-238
16. Kamiguchi Y, Mikamo K (1986): An improved efficient method for analyzing human sperm chromosomes using zona-free hamster ova. Am J Hum Genet 38: 724-740
17. Martin RH, Lin CC, Balkan W, Burns K (1982): Direct chromosomal analysis of human spermatozoa: Preliminary results from 18 normal men. Am J Hum Genet 34: 459-468
18. Martin RH (1985): Chromosomal abnormalities in human sperm. In: Dellarco VL, Voytek PE, Hollaender A (eds). Aneuploidy etiology and mechanisms. Basic life sciences. Vol 36. Plenum Press, New York, pp 91-102
19. Miharu N, Best RG, Young SR (1994): Numerical chromosome abnormalities in spermatozoa of fertile and infertile men detected by fluorescence in situ hybridization. Hum Genet 93: 502-506
20. Robbins WA, Segrave R, Pinkel D, Wyrobek AJ (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
21. Rodman TC, Pruslin FH, Allfrrey VG (1982): Mechanisms of displacement of sperm basic nuclear proteins in mammals. An in vitro simulation of post fertilization results. J Cell Sei 53: 227-244
22. Rudak E, Jacobs PA, Yanagimachi R (1978): Direct analysis of chromosome constitution of human spermatozoa. Nature 274: 911-913
23. Williams BJ, Ballenger CA. Malter HE, Bishop F. Tucker M, Zwingmari TA, Hassold TJ ( 1993): Non-disjunction in human sperm: results of fluorescence in situ hybridization studies using two and three probes. Hum Mol Genet 2: 1929-1936
24. World Health Organization (1987): WHO laboratory manual for the examination of human semen and semen-cervical mucus interaction. 2nd ed. Cambridge Univ Press. New York, pp 3-10
25. Wyrobek AJ, Alhborn T, Balhorn R, Stanker L, Pinkel D (1990): Fluorescence in situ hybridization to Y chromosome in decondensed human sperm nuclei. Mol Reprod Dev 27: 200-208
26. Wyrobek AJ. Robbins WA, Mehraein Y. Pinkel D, Weier HU (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