Volkert F C, Broach J R
Cell. 1986 Aug 15;46(4):541-50. doi: 10.1016/0092-8674(86)90879-2.
All stable, naturally occurring circular yeast DNA plasmids contain a pair of long, nontandem inverted repeats that undergo frequent reciprocal recombination. This yields two plasmid inversion isomers that exist in the cell in equal numbers. In the 2 mu circle plasmid of S. cerevisiae such inversion is catalyzed by a plasmid-encoded site-specific recombinase, FLP. We show that the site-specific recombination system of 2 mu circle enables the plasmid to increase its mean intracellular copy number in yeast cells growing under nonselective conditions. This apparently occurs by a FLP-induced transient shift in the mode of replication from theta to double rolling circle as initially proposed by Futcher. This capability may ensure stable maintenance of the plasmid by enabling it to correct downward deviations in copy number that result from imprecision of the plasmid-encoded partitioning system.
所有稳定的、天然存在的环状酵母DNA质粒都包含一对长的、非串联的反向重复序列,它们会频繁地进行相互重组。这产生了两种质粒倒位异构体,它们在细胞中以相等的数量存在。在酿酒酵母的2μm环状质粒中,这种倒位由质粒编码的位点特异性重组酶FLP催化。我们表明,2μm环状质粒的位点特异性重组系统使该质粒能够在非选择性条件下生长的酵母细胞中增加其平均细胞内拷贝数。这显然是通过FLP诱导的复制模式从θ型到双滚环的瞬时转变而发生的,这是Futcher最初提出的。这种能力可以通过使质粒纠正由于质粒编码的分配系统不精确而导致的拷贝数向下偏差,从而确保质粒的稳定维持。