Krude T, Knippers R
Fakultät für Biologie, Universität Konstanz, Federal Republic of Germany.
Chromosoma. 1992;102(1 Suppl):S83-92. doi: 10.1007/BF02451790.
We operationally define two forms of SV40 minichromosomes, a 75S-form, prepared at low salt concentration, referred to as native minichromosomes, and a 50S-form, obtained after treatment with 0.5 M potassium acetate, the salt-treated minichromosomes. Both preparations of minichromosomes serve well as templates for replication in vitro. Their respective replication products are strikingly different: replicated native minichromosomes contain a densely packed array of the maximal number of nucleosomes whereas replicated salt-treated minichromosomes carry, on average, half of the maximal number. We conclude that in both cases parental nucleosomes are transferred to progeny DNA, and, in addition, that an assembly of new nucleosomes occurs during the replication of native minichromosomes. This is apparently due to the presence of a nucleosome assembly factor as a constituent of native minichromosomes that dissociates upon treatment with salt. We further show that preparations of minichromosomes usually contain significant amounts of copurifying hnRNP particles and SV40 virion precursor particles. However, these structures do not detectably affect the replication and the chromatin assembly reactions.
我们从操作上定义了两种形式的SV40微型染色体,一种是在低盐浓度下制备的75S形式,称为天然微型染色体,另一种是用0.5M醋酸钾处理后得到的50S形式,即盐处理微型染色体。这两种微型染色体制剂都能很好地作为体外复制的模板。它们各自的复制产物显著不同:复制的天然微型染色体含有紧密排列的最大数量的核小体,而复制的盐处理微型染色体平均携带最大数量的一半。我们得出结论,在这两种情况下,亲代核小体都转移到子代DNA上,此外,在天然微型染色体的复制过程中会发生新核小体的组装。这显然是由于作为天然微型染色体组成成分的核小体组装因子的存在,该因子在盐处理后会解离。我们进一步表明,微型染色体制剂通常含有大量共纯化的hnRNP颗粒和SV40病毒体前体颗粒。然而,这些结构对复制和染色质组装反应没有可检测到的影响。