ABSTRACT
It is accepted that recombination errors during human female meiotic prophase have some influence on the origin of trisomy 21. A total of 335 oocytes from four euploid fetuses were analysed by immunofluorescence and fluorescence in-situ hybridization in order to assess the recombination nodules along chromosome 21. Results based on the analysis of recombination points on the bivalent 21 during human female meiosis showed that both number [none (3.70%), one (79.01%) and two (17.29%)1 and distribution (always positioned interstitially on the q-arm) are different in males, ensuring that the two homologues more efficiently remain together until anaphase 1.Therefore, the mainly maternal origin of trisomy 21 appears not be linked to the first stages of oocyte development during fetal life, and this leads to the suggestion that the influence of environmental factors on the segregation of chromosome 21 homologues in later meiotic stages could have a significant role in the predominant maternal origin of trisomy 21.
Subject(s)
Chromosomes, Human, Pair 21 , Pachytene Stage , Recombination, Genetic , Female , Fluorescent Antibody Technique , Humans , In Situ Hybridization, Fluorescence , MaleABSTRACT
The processes of synapsis and synaptic adjustment have been detected in some structural and numerical anomalies in two female rat foetuses and in one male rat in the course of a study on X-ray genotoxicity. The synaptic characteristics and adjustment of one pericentric inversion and a deletion have been analysed by electron microscopy in synaptonemal complex spreads from two female foetuses, and the synaptic behaviour of a trisomy has been studied in a testicular biopsy from an adult male. In a large proportion (from 50% to 90%) of the analysed cells, the abnormal meiotic configuration could not be detected either because the anomaly was present in mosaic from trisomy or because synaptic adjustment had already taken place (inversion) or as result of a combination of two of the above (deletion).
