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Journal of Andrology, Vol 14, Issue 4 282-288, Copyright © 1993 by The American Society of Andrology
JOURNAL ARTICLE |
A. M. Estop, S. Munne, L. K. Jost and D. P. Evenson
Department of Medical Genetics, West Penn Hospital, Pittsburgh, Pennsylvania 15224.
Mouse epididymal sperm incubated in Tyrode's T6 fertilization media were analyzed over time for chromosome damage by two methods. First, cytogenetic analysis was done on paternal pronuclei metaphase chromosomes. After 6 hours incubation 11% of the cells demonstrated chromosome structural abnormalities. Secondly, sperm nuclei were measured by the sperm chromatin structure assay, which is a measure of the susceptibility of sperm DNA to the nuclei demonstrated an increased susceptibility to DNA denaturation, reaching near 100% by 48 hours. Changes in chromatin structure at the molecular level may lead to chromosome breaks seen in pronuclear chromosomes.
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