Takeda Y, Hirokawa H, Nagata T
Institute for Biochemical Regulation, School of Agriculture, Nagoya University, Japan.
Mol Gen Genet. 1992 Mar;232(2):191-8. doi: 10.1007/BF00279996.
When tobacco suspension culture line BY2 cells in stationary phase are transferred into fresh medium, replication of proplastid DNA proceeds for 24 h in the absence of nuclear DNA replication. Replicative intermediates of the proplastid DNA concentrated by benzoylated, naphthoylated DEAE cellulose chromatography, were radioactively labelled and hybridized to several sets of restriction endonuclease fragments of tobacco chloroplast DNA. The intermediates hybridized preferentially to restriction fragments in the two large inverted repeats. Mapping of D-loops and of restriction fragment lengths by electron microscopy permitted the localization of the replication origin, which was close to the 23S rRNA gene in the inverted repeats. The replication origins in both segments of the inverted repeat in tobacco proplastid DNA were active in vivo.
当处于静止期的烟草悬浮培养系BY2细胞转移到新鲜培养基中时,质体前体DNA的复制在没有核DNA复制的情况下持续进行24小时。通过苯甲酰化、萘甲酰化二乙氨基乙基纤维素色谱法浓缩的质体前体DNA的复制中间体,经放射性标记后与烟草叶绿体DNA的几组限制性内切酶片段杂交。这些中间体优先与两个大的反向重复序列中的限制性片段杂交。通过电子显微镜对D环和限制性片段长度进行定位,从而确定了复制起点的位置,该起点靠近反向重复序列中的23S rRNA基因。烟草质体前体DNA反向重复序列两个区段中的复制起点在体内均具有活性。