Literature DB >> 3356166

An analysis of structural aberrations in human sperm chromosomes.

B F Brandriff1, L A Gordon, D Moore, A V Carrano.   

Abstract

We have analyzed structural aberrations in 5,000 sperm chromosome complements obtained from 20 men over a 5-yr period by fusion of human sperm with hamster eggs. Detailed data are presented on 366 abnormal cells with 379 analyzable breakpoints. The frequency of cells with structural aberrations ranged from 1.9% to 14.5% among donors; this interindividual variability was statistically significant (p less than 0.0001). In contrast, repeat samples from individual men showed no significant variation over time. The number of sperm chromosome sets processed per hamster egg had no effect on the frequency with which structural aberrations occurred, nor were sperm chromosome abnormalities altered by varying capacitation or culture conditions. The spectrum of structural aberrations observed in human sperm chromosomes and a chi-square analysis of breakpoints based on DNA content are presented. Although human sperm chromosome abnormalities were visualized with a cross-species system, we believe that they represent an inherent, biologically significant phenomenon.

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Mesh:

Year:  1988        PMID: 3356166     DOI: 10.1159/000132500

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN: 0301-0171


  16 in total

1.  Repair of human sperm chromosome aberrations in the hamster egg.

Authors:  A Genescà; M R Caballín; R Miró; J Benet; J R Germà; J Egozcue
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

2.  Cytogenetic studies in human sperm.

Authors:  A M Estop; K Cieply; V Vankirk; S Munne; K Garver
Journal:  Hum Genet       Date:  1991-08       Impact factor: 4.132

3.  Determination of Y chromosome aneuploidy in human sperm nuclei by nonradioactive in situ hybridization.

Authors:  M Guttenbach; M Schmid
Journal:  Am J Hum Genet       Date:  1990-03       Impact factor: 11.025

4.  Advanced age increases chromosome structural abnormalities in human spermatozoa.

Authors:  Cristina Templado; Anna Donate; Jesús Giraldo; Mercè Bosch; Anna Estop
Journal:  Eur J Hum Genet       Date:  2010-11-03       Impact factor: 4.246

5.  Meiotic segregation, recombination, and gamete aneuploidy assessed in a t(1;10)(p22.1;q22.3) reciprocal translocation carrier by three- and four-probe multicolor FISH in sperm.

Authors:  P Van Hummelen; D Manchester; X Lowe; A J Wyrobek
Journal:  Am J Hum Genet       Date:  1997-09       Impact factor: 11.025

6.  Cytogenetic studies in motile sperm from normal men.

Authors:  J Benet; A Genescà; J Navarro; J Egozcue; C Templado
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

7.  The male-derived genome after sperm-egg fusion: spatial distribution of chromosomal DNA and paternal-maternal genomic association.

Authors:  B F Brandriff; L A Gordon; R Segraves; D Pinkel
Journal:  Chromosoma       Date:  1991-05       Impact factor: 4.316

8.  Significance of structural chromosome aberrations in human sperm: analysis of induced aberrations.

Authors:  A Genescà; J Benet; M R Caballín; R Miró; J R Germà; J Egozcue
Journal:  Hum Genet       Date:  1990-10       Impact factor: 4.132

9.  Incidence of chromosome 3, 7, 10, 11, 17 and X disomy in mature human sperm nuclei as determined by nonradioactive in situ hybridization.

Authors:  M Guttenbach; R Schakowski; M Schmid
Journal:  Hum Genet       Date:  1994-01       Impact factor: 4.132

10.  Chromosome aberrations in 450 sperm complements from eight controls and lack of increase after chemotherapy in two patients.

Authors:  J Jenderny; M L Jacobi; A Rüger; G Röhrborn
Journal:  Hum Genet       Date:  1992 Sep-Oct       Impact factor: 4.132

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