Macieira-Coelho A, Bengtsson A, Van der Ploeg M
Histochemistry. 1982;75(1):11-24. doi: 10.1007/BF00492529.
The segregation of DNA at the time of cell division was analysed by measuring the DNA contents of cells in mitosis and the incorporation of tritiated thymidine (3H-TdR) on each half of anaphases and telophases. Results suggest that the spreads in the 2C and 4C DNA contents are due to quantitative differences which could originate during semi-conservative DNA synthesis, chromosome assembly and chromosome segregation. This continuous rearrangement of the genome could lead either to a degenerative process or to a differentiation program.
通过测量有丝分裂细胞的DNA含量以及在后期和末期的每一半中氚标记胸腺嘧啶核苷(3H-TdR)的掺入情况,分析了细胞分裂时DNA的分离。结果表明,2C和4C DNA含量的分布是由于数量差异造成的,这些差异可能源于半保留DNA合成、染色体组装和染色体分离过程中。基因组的这种持续重排可能导致退化过程或分化程序。