Nondisjunction in human sperm: Comparison of frequencies in acrocentric chromosomes

Renée H. Martin*, A. W. Rademaker

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

19 Scopus citations

Abstract

Acrocentric chromosomes may be particularly predisposed to nondisjunction because of the frequency of trisomy for these chromosomes in human spontaneous abortions and liveborns. Studies of aneuploidy in human sperm have provided data on only a few acrocentric chromosomes, with evidence that chromosome 21 has a significantly increased frequency of disomy. To determine whether other acrocentric chromosomes have a higher frequency of nondisjunction or if chromosome 21 is anomalous, disomy frequencies for chromosomes 13 and 22 were studied by fluorescence in situ hybridization (FISH) analysis of 51,043 sperm nuclei from five normal men for whom the frequency of disomy for chromosomes 15 and 21 was known. The mean frequency of disomy for chromosome 13 (0.19%) did not differ significantly from that for other autosomes; however, the frequency of disomy 22 (1.21%) was significantly elevated (P < 0.001, Mantel-Haenszel χ2 test). The G-group chromosomes (Nos. 21 and 22) also showed a significantly increased frequency of disomy (0.75%) compared to acrocentric D-group chromosomes (viz., chromosomes 13 and 15; 0.15%) (P < 0.001, Mantel-Haenszel χ2 test) and other autosomes (chromosomes 1, 2, 4, 9, 12, 13, 15, 16, 18, and 20; 0.13%) studied in the same men (P < 0.001, Mantel-Haenszel χ2 test).

Original languageEnglish (US)
Pages (from-to)43-45
Number of pages3
JournalCytogenetics and Cell Genetics
Volume86
Issue number1
DOIs
StatePublished - 1999

ASJC Scopus subject areas

  • Genetics
  • Cell Biology

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