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DNA and chromatin structure
Author(s) -
Sylvie Mercier,
Frédéric Morel,
Claude Roux,
Marie Claire Clavequin,
J.L. Bresson
Publication year - 1996
Publication title -
molecular human reproduction
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 1.143
H-Index - 122
eISSN - 1460-2407
pISSN - 1360-9947
DOI - 10.1093/molehr/2.7.485
Subject(s) - biology , aneuploidy , fluorescence in situ hybridization , y chromosome , x chromosome , offspring , chromosome , chromatin , in situ hybridization , fish <actinopterygii> , genetics , karyotype , microbiology and biotechnology , dna , andrology , gene , pregnancy , gene expression , medicine , fishery
The sex chromosomes in spermatozoa of a 47,XYY fertile male were analysed simultaneously by dual fluorescence in-situ hybridization (FISH), with two probes (pHY2.1 and pXBR). Of the 1 cells analysed, 95179 spermatozoa (95.18%) exhibited one or more hybridization signals. Of the hybridized nuclei, 85.37% showed a normal sex chromosome constitution (37.37% X-bearing cells and 48.00% Y-bearing cells), with an X:Y ratio of 0.78:1. A total of 14.63% of the hybridized nuclei exhibited sex chromosome aneuploidy with a majority of XY- and YY-bearing spermatozoa (9.37 and 4.65% respectively). Even if the majority of spermatozoa have chromosomal haploidy, a large proportion of them exhibits numerical errors for the sex chromosomes. These observations raise questions about the commonly-admitted notions concerning the absence of chromosomal risk for XYY male offspring.

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