Taketo M, Jazwinski S M, Edelman G M
Proc Natl Acad Sci U S A. 1980 Jun;77(6):3144-8. doi: 10.1073/pnas.77.6.3144.
The 2-micron DNA plasmid cosedimented in sucrose gradients with the folded chromosome on centrifugation of lysates from logarithmically growing yeast cells. It banded with both the slow-sedimenting g1 form derived from prereplicative cells and the fast-sedimenting g2 form from postreplicative cells. When cells were induced to withdraw from the cell cycle by nitrogen starvation, the folded chromosome was converted to the g0 form, which sedimented more slowly than the g1 form, and only 1/10th the amount of 2-micron DNA cosedimented with this g0 form as compared to the logarithmic-phase forms, g1 and g2. Expression of the temperature-sensitive cell division cycle (cdc) 28 mutation, which defines the "start" of the cell cycle, resulted in a rapid alteration in the folded chromosome sedimentation pattern, and less than 20% of the 2-micron DNA cosedimented with the folded chromosome. These results raise the possibility that association of the 2-micron DNA plasmid with structures in the cell corresponding to the folded chromosome is subject to cell division cycle control.
对数生长期酵母细胞裂解物经离心后,2 微米 DNA 质粒与折叠染色体在蔗糖梯度中共沉降。它与来自复制前细胞的沉降较慢的 g1 形式以及来自复制后细胞的沉降较快的 g2 形式一起形成条带。当细胞通过氮饥饿被诱导退出细胞周期时,折叠染色体转变为 g0 形式,其沉降速度比 g1 形式慢,并且与对数期形式 g1 和 g2 相比,只有 1/10 的 2 微米 DNA 与这种 g0 形式共沉降。定义细胞周期“起始”的温度敏感型细胞分裂周期(cdc)28 突变的表达导致折叠染色体沉降模式迅速改变,并且只有不到 20%的 2 微米 DNA 与折叠染色体共沉降。这些结果增加了一种可能性,即 2 微米 DNA 质粒与细胞中对应于折叠染色体的结构的关联受细胞分裂周期控制。