Abstract
Meiosis of T70H/+, Ts(113)70H translocation trisomic male mice has been studied using C-banded preparations and 3H-thymidine autoradiography of the first meiotic division. Epididymal sperm counts and sperm morphology scores were also collected. As reported earlier, at the first meiotic division the translocation involved chromosomes 1, 13, 131 and 113 (twice) formed mainly three multivalent configurations: Chain III+II, CIV+I and CV. — The autoradiographic study indicated an abnormal, precocious spiralization pattern for the chromatin in CIV+I primary spermatocytes. These cells, occurring together with the CIII+II and CV configurations in recognizable groups, usually descending from single spermatogonial stem cells, are delayed through meiotic prophase. Both delay and disturbed chromosome spiralization in these cells are attributed to the uniform association of the univalent (I) chromosome 113 with the sex chromosomes during pachytene. Primary spermatocytes of the CIV+I configuration and those carrying a CV take longer to develop from metaphase I into secondary spermatocytes than does the CIII+II type. — In T70H tertiary trisomics with a similar chromosome imbalance, the majority of primary spermatocytes degenerates during the diakinesis-metaphase I stages of meiosis. Fertility is low in contrast to the translocation trisomics. Comparison between the two types leads to the conclusion, that trisomy per se reduces the size of the testes and that the univalent containing CIV+I primary spermatocytes, contrary to the almost uniformly 113 univalent carrying spermatocytes of the T70H tertiary trisomics are rescued by the neighbouring CIII+II and CV carrying cells to form normal secondary spermatocytes and morphologically normal sperm.
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de Boer, P., Speed, R.M. Meiosis of T70H translocation trisomic male mice. Chromosoma 87, 315–325 (1982). https://doi.org/10.1007/BF00327633
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DOI: https://doi.org/10.1007/BF00327633