Daentl D L, Erickson R P, Betlach C J
Differentiation. 1977 Oct 13;8(3):159-66. doi: 10.1111/j.1432-0436.1977.tb00932.x.
Spermatogenic cells separated by velocity sedimentation were analysed by a micro-procedure for differentiation-associated changes in DNA synthetic capabilities. DNA-dependent DNA polymerase activity is maximal in premeiotic and meiotic cells, sequentially declines in progressively more differentiated spermiogenic cells to a minimum value in testicular spermatozoa which is 1/14 of the maximum. No further decrease of activity is observed during the subsequent process of sperm cell maturation and, at the end-differentiated state, the potential of sperm cells for DNA synthesis is demonstrated by the presence of substantial activities of thymidine and thymidylate kinases as well as DNA polymerase activity, as determined by in vitro assay, are polymerase. Although levels of DNA polymerase activity, as determined by in vitro assay, are negatively correlated with the state of differentiation, the findings support the hypothesis that, in this cell system, DNA synthetic enzymes may not be limiting factors in the control of DNA synthesis.
通过速度沉降分离的生精细胞,采用微程序分析其DNA合成能力与分化相关的变化。DNA依赖性DNA聚合酶活性在减数分裂前和减数分裂细胞中最高,在逐渐分化的精子发生细胞中依次下降,在睾丸精子中降至最低值,仅为最高值的1/14。在随后的精子细胞成熟过程中未观察到活性进一步降低,并且在终末分化状态下,通过体外测定确定,精子细胞的DNA合成潜力通过胸苷和胸苷酸激酶的大量活性以及DNA聚合酶活性得以证明。尽管通过体外测定确定的DNA聚合酶活性水平与分化状态呈负相关,但这些发现支持以下假设:在这个细胞系统中,DNA合成酶可能不是控制DNA合成的限制因素。