Fluorescence In Situ Hybridization with Chromosome Paint Probes: A Novel Approach To Assess Aneuploidy in Human Sperm Nuclei

作者: N. Rives , S. Wust , B. David , V. Duchesne , G. Joly

DOI: 10.1023/A:1022549713692

关键词: Mean frequencyFish <Actinopterygii>SpermAneuploidyChromosomePloidyBiologyFluorescence in situ hybridizationMolecular probeMolecular biology

摘要: Purpose: Fluorescence in situ hybridization (FISH) using whole-chromosome paint probes was performed to evaluate disomy and diploidy frequency for chromosomes 1, 18, 19, 22 human sperm nuclei. Methods: Ten subjects of proven fertility normal spermatic parameters were included the study. A dual-color FISH method carried out. Results: total 157,896 spermatozoa scored. The mean frequencies disomic 0.22% (range, 0.19 0.28%), 0.24% 0.14 0.37%), 0.17 0.30%), 0.25% 0.21 0.29%), respectively. 0.14% 0.09 0.18%). No interindividual interchromosomal variations aneuploidy observed between different subjects. Conclusions: with provides a novel efficient approach assessment nuclei.

参考文章(41)
A J Wyrobek, W A Robbins, D Pinkel, R Segraves, 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 American Journal of Human Genetics. ,vol. 52, pp. 799- 807 ,(1993)
A. W. Rademaker, E. L. Spriggs, R. H. Martin, Aneuploidy in human sperm : The use of multicolor FISH to test various theories of nondisjunction American Journal of Human Genetics. ,vol. 58, pp. 356- 362 ,(1996)
F. Pellestor, B. Andréo, A. Girardet, J. P. Charlieu, L. Coignet, Assessment of aneuploidy for chromosomes 8, 9, 13, 16, and 21 in human sperm by using primed in situ labeling technique. American Journal of Human Genetics. ,vol. 58, pp. 797- 802 ,(1996)
Edith Coonen, Math H. E. C. Pieters, John C. M. Dumoulin, Henk Meyer, Johannes L. H. Evers, Frans C. S. Ramaekers, Joep P. M. Geraedts, Nonisotopic in situ hybridization as a method for nondisjunction studies in human spermatozoa. Molecular Reproduction and Development. ,vol. 28, pp. 18- 22 ,(1991) , 10.1002/MRD.1080280104
JanetM. Holmes, ReneeH. Martin, Aneuploidy detection in human sperm nuclei using fluorescence in situ hybridization. Human Genetics. ,vol. 91, pp. 20- 24 ,(1993) , 10.1007/BF00230216
F. Pellestor, A. Girardet, B. Andr&eacute;o, G. Lefort, J.P. Charlieu, Incidence of chromosome 1 disomy in human sperm estimated by the primed in situ (PRINS) labeling technique Cytogenetic and Genome Research. ,vol. 76, pp. 192- 195 ,(1997) , 10.1159/000134547
F.Z. Bischoff, D.D. Nguyen, K.J. Burt, L.G. Shaffer, Estimates of aneuploidy using multicolor fluorescence in situ hybridization on human sperm. Cytogenetic and Genome Research. ,vol. 66, pp. 237- 243 ,(1994) , 10.1159/000133702
Renée H. Martin, Evelyn Ko, Alfred Rademaker, Distribution of aneuploidy in human gametes: comparison between human sperm and oocytes. American Journal of Medical Genetics. ,vol. 39, pp. 321- 331 ,(1991) , 10.1002/AJMG.1320390315
A. C. Chandley, T.B. Hargreave, Genetic anomaly and ICSI. Human Reproduction. ,vol. 11, pp. 930- 932 ,(1996) , 10.1093/OXFORDJOURNALS.HUMREP.A019323
Andrew J. Wyrobek, Thomas Alhborn, Rod Balhorn, Larry Stanker, Daniel Pinkel, Fluorescence in situ hybridization to Y chromosomes in decondensed human sperm nuclei. Molecular Reproduction and Development. ,vol. 27, pp. 200- 208 ,(1990) , 10.1002/MRD.1080270304