Aquiles Sanchez J, Wonsey D R, Harris L, Morales J, Wangh L J
Department of Biology, Brandeis University, Waltham, Massachusetts 02254, USA.
J Biol Chem. 1995 Dec 15;270(50):29676-81. doi: 10.1074/jbc.270.50.29676.
Small plasmids replicate efficiently in unfertilized Xenopus eggs provided they are injected before rather than after activation of the cell cycle. Here we use Xenopus egg extracts to test the hypothesis that efficient replication results from chromatin assembly prior to activation giving preloaded plasmids a head start toward the formation of a replicating pseudonucleus (Sanchez, J.A., Marek, D., and Wangh, L.J. (1992) J. Cell Sci. 103, 907-918). As in ovum, plasmid DNA preincubated in unactivated egg cytoplasmcytostatic factor extracts) replicate more efficiently after extract activation than does the same DNA added to the same extract after activation. Unlike in ovum, however, plasmids that replicate efficiently in vitro do not assemble into chromatin during preincubation and become topologically knotted instead. But even DNA knotting does not explain subsequent efficient replication. Also, plasmids preassembled into chromatin in vitro do not replicate efficiently in activated egg cytoplasm unless first preincubated in a CSF extract. We conclude that unactivated eggs contain replication-enhancing activities that can act independently of plasmid chromatin assembly and DNA topology. These postulated "preloading" factor(s) may be related to licensing factor, an activity that controls initiation of DNA replication in eukaryotic cells. The experimental conditions described here will permit characterization of preloading/licensing factor(s) in the context of a small plasmid substrate.
小质粒在未受精的非洲爪蟾卵中能高效复制,前提是在细胞周期激活之前而非之后注射。在此,我们利用非洲爪蟾卵提取物来检验这一假说:高效复制源于激活前的染色质组装,使预先加载的质粒在形成复制性假核方面占得先机(桑切斯,J.A.,马雷克,D.,以及王赫,L.J.(1992年)《细胞科学杂志》103卷,907 - 918页)。与在卵细胞中一样,在未激活的卵细胞质(细胞静止因子提取物)中预孵育的质粒DNA,在提取物激活后比激活后添加到相同提取物中的相同DNA复制效率更高。然而,与卵细胞不同的是,在体外能高效复制的质粒在预孵育过程中不会组装成染色质,而是形成拓扑缠结。但即使是DNA缠结也无法解释随后的高效复制。此外,在体外预组装成染色质的质粒在激活的卵细胞质中不能高效复制,除非首先在细胞静止因子提取物中预孵育。我们得出结论,未激活的卵含有复制增强活性,其作用可独立于质粒染色质组装和DNA拓扑结构。这些假定的“预加载”因子可能与许可因子有关,许可因子是一种控制真核细胞DNA复制起始的活性物质。本文所述的实验条件将有助于在小质粒底物的背景下对预加载/许可因子进行表征。