Laskey R A, Mills A D, Morris N R
Cell. 1977 Feb;10(2):237-43. doi: 10.1016/0092-8674(77)90217-3.
A cell-free system is described which assembles chromatin from purified DNA in 1 hr under physiological incubation conditions. It consists of a 145,000 x g (maximum) supernatant fraction from eggs of Xenopus laevis. It converts SV40 DNA to a nucleoprotein which co-sediments with naturally occurring SV40 chromatin and which can be cleaved by micrococcal nuclease to a highly ordered pattern of DNA fragments resembling those from digestion of liver chromatin. It inserts superhelical turns into relaxed, covalently closed DNA. The assembly process is not cooperative. Under limiting conditions, each DNA molecule becomes partially assembled. Assembly does not require replication of the DNA or protein synthesis, but occurs from a stored histone pool of at least 40 ng per egg. Under conditions of DNA excess, assembly becomes dependent upon the amount of exogenous histones added to the incubation. Apart from histones and a nicking-closing activity, chromatin assembly requires an additonal thermolabile factor which is present in the egg supernatant.
本文描述了一种无细胞体系,该体系在生理孵育条件下,可在1小时内从纯化的DNA组装染色质。它由非洲爪蟾卵的145,000×g(最大值)上清液组分组成。它将SV40 DNA转化为一种核蛋白,该核蛋白与天然存在的SV40染色质共沉降,并且可以被微球菌核酸酶切割成高度有序的DNA片段模式,类似于肝脏染色质消化产生的片段。它将超螺旋引入松弛的、共价闭合的DNA中。组装过程不具有协同性。在有限条件下,每个DNA分子都会部分组装。组装不需要DNA复制或蛋白质合成,而是从每个卵至少40 ng的储存组蛋白库中发生。在DNA过量的条件下,组装变得依赖于孵育中添加的外源组蛋白的量。除了组蛋白和切口封闭活性外,染色质组装还需要卵上清液中存在的一种额外的热不稳定因子。