Blow J J
ICRF Clare Hall Laboratories, Potters Bar, Herts, England.
J Cell Biol. 1993 Sep;122(5):993-1002. doi: 10.1083/jcb.122.5.993.
Xenopus egg extracts treated with the protein kinase inhibitor 6-dimethylaminopurine (6-DMAP) are unable to support the initiation of DNA replication. Nuclei assembled in 6-DMAP extracts behave as though they are in G2, and will not undergo another round of DNA replication until passage through mitosis. 6-DMAP extracts are functionally devoid of a replication factor that modifies chromatin in early G1 before nuclear envelope assembly, but which is itself incapable of crossing the nuclear envelope. This chromatin modification is capable of supporting only a single round of semiconservative replication. The behavior of this replication factor is sufficient to explain why eukaryotic DNA is replicated once and only once in each cell cycle, and conforms to the previous model of a Replication Licensing Factor. Cell cycle analysis shows that this putative Licensing Factor is inactive during metaphase, but becomes rapidly activated on exit from metaphase when it can modify chromatin before nuclear envelope assembly is complete.
用蛋白激酶抑制剂6 - 二甲基氨基嘌呤(6 - DMAP)处理的非洲爪蟾卵提取物无法支持DNA复制的起始。在6 - DMAP提取物中组装的细胞核表现得就好像它们处于G2期,并且在经历有丝分裂之前不会进行另一轮DNA复制。6 - DMAP提取物在功能上缺乏一种复制因子,该因子在核膜组装之前的G1早期修饰染色质,但自身无法穿过核膜。这种染色质修饰仅能支持一轮半保留复制。这种复制因子的行为足以解释为什么真核生物的DNA在每个细胞周期中只复制一次且仅复制一次,并且符合先前的复制许可因子模型。细胞周期分析表明,这种假定的许可因子在中期处于无活性状态,但在从中期退出时会迅速被激活,此时它可以在核膜组装完成之前修饰染色质。