Gillespie P J, Blow J J
CRC Chromosome Replication Research Group, Division of Gene Regulation,Department of Biochemistry, University of Dundee, Dundee DD1 5EH, UK.
Nucleic Acids Res. 2000 Jan 15;28(2):472-80. doi: 10.1093/nar/28.2.472.
During late mitosis and early G(1), a series of proteins are assembled onto replication origins, resulting in them becoming 'licensed' for replication in the subsequent S phase. Four factors have so far been identified that are required for chromatin to become functionally licensed: ORC (the origin recognition complex) and Cdc6, plus the two components of the replication licensing system RLF-M and RLF-B. Here we describe the first steps of a systematic fractionation of Xenopus egg extracts to identify all the components necessary for the assembly of licensed replication origins on Xenopus sperm nuclei (the physiological DNA substrate in this system). We have purified a new activity essential for this reaction, and have shown that it is nucleoplasmin, a previously known chromatin remodelling protein. Nucleoplasmin decondenses the sperm chromatin by removing protamines, and is required at the earliest known step in origin assembly to allow ORC to bind to the DNA. Sperm nuclei can be licensed by a combination of nucleoplasmin, RLF-M and a partially purified fraction that contains ORC, Cdc6 and RLF-B. This suggests that we are likely to have identified most of the proteins required for this assembly reaction.
在有丝分裂后期和G1早期,一系列蛋白质组装到复制起点上,使其在随后的S期具备复制“许可”。目前已鉴定出四种使染色质获得功能许可所需的因子:ORC(起点识别复合体)、Cdc6,以及复制许可系统的两个组分RLF-M和RLF-B。在此,我们描述了对非洲爪蟾卵提取物进行系统分级分离的初步步骤,以鉴定在非洲爪蟾精子细胞核(此系统中的生理性DNA底物)上组装有许可的复制起点所需的所有组分。我们纯化了此反应所必需的一种新活性物质,并证明它是核质蛋白,一种先前已知的染色质重塑蛋白。核质蛋白通过去除鱼精蛋白使精子染色质解聚,并且在起点组装的最早已知步骤中是必需的,以便ORC能够结合到DNA上。精子细胞核可以通过核质蛋白、RLF-M和一个含有ORC、Cdc6和RLF-B的部分纯化组分的组合来获得许可。这表明我们很可能已经鉴定出了此组装反应所需的大部分蛋白质。