Gruss C, Sogo J M
Institute for Cell Biology, ETH Zürich, Switzerland.
Bioessays. 1992 Jan;14(1):1-8. doi: 10.1002/bies.950140102.
Just as the faithful replication of DNA is an essential process for the cell, chromatin structures of active and inactive genes have to be copied accurately. Under certain circumstances, however, the activity pattern has to be changed in specific ways. Although analysis of specific aspects of these complex processes, by means of model systems, has led to their further elucidation, the mechanisms of chromatin replication in vivo are still controversial and far from being understood completely. Progress has been achieved in understanding: 1. The initiation of chromatin replication, indicating that a nucleosome-free origin is necessary for the initiation of replication; 2. The segregation of the parental nucleosomes, where convincing data support the model of random distribution of the parental nucleosomes to the daughter strands; and 3. The assembly of histones on the newly synthesized strands, where growing evidence is emerging for a two-step mechanism of nucleosome assembly, starting with the deposition of H3/H4 tetramers onto the DNA, followed by H2A/H2B dimers.
正如DNA的忠实复制是细胞的一个基本过程一样,活跃基因和非活跃基因的染色质结构也必须被精确复制。然而,在某些情况下,活性模式必须以特定方式改变。尽管通过模型系统对这些复杂过程的特定方面进行分析有助于进一步阐明它们,但体内染色质复制的机制仍然存在争议,远未被完全理解。在以下方面取得了进展:1. 染色质复制的起始,表明无核小体的起始点对于复制起始是必要的;2. 亲代核小体的分离,有令人信服的数据支持亲代核小体随机分布到子链的模型;3. 组蛋白在新合成链上的组装,越来越多的证据表明核小体组装存在两步机制,首先是H3/H4四聚体沉积到DNA上,然后是H2A/H2B二聚体。