Guerrini A M, Ascenzioni F, Tribioli C, Donini P
EMBO J. 1985 Jun;4(6):1569-73. doi: 10.1002/j.1460-2075.1985.tb03818.x.
Linear plasmids were constructed by adding telomeres prepared from Tetrahymena pyriformis rDNA to a circular hybrid Escherichia coli-yeast vector and transforming Saccharomyces cerevisiae. The parental vector contained the entire 2 mu yeast circle and the LEU gene from S. cerevisiae. Three transformed clones were shown to contain linear plasmids which were characterized by restriction analysis and shown to be rearranged versions of the desired linear plasmids. The plasmids obtained were imperfect palindromes: part of the parental vector was present in duplicated form, part as unique sequences and part was absent. The sequences that had been lost included a large portion of the 2 mu circle. The telomeres were approximately 450 bp longer than those of T. pyriformis. DNA prepared from transformed S. cerevisiae clones was used to transform Schizosaccharomyces pombe. The transformed S. pombe clones contained linear plasmids identical in structure to their linear parents in S. cerevisiae. No structural re-arrangements or integration into S. pombe was observed. Little or no telomere growth had occurred after transfer from S. cerevisiae to S. pombe. A model is proposed to explain the genesis of the plasmids.
通过将从梨形四膜虫rDNA制备的端粒添加到环状杂交大肠杆菌-酵母载体中并转化酿酒酵母,构建了线性质粒。亲本载体包含完整的2μm酵母环和来自酿酒酵母的LEU基因。三个转化克隆显示含有线性质粒,通过限制性分析对其进行了表征,并显示为所需线性质粒的重排版本。获得的质粒是不完全回文:亲本载体的一部分以重复形式存在,一部分作为独特序列存在,一部分缺失。丢失的序列包括2μm环的大部分。这些端粒比梨形四膜虫的端粒长约450bp。从转化的酿酒酵母克隆制备的DNA用于转化粟酒裂殖酵母。转化的粟酒裂殖酵母克隆含有与其酿酒酵母线性亲本结构相同的线性质粒。未观察到结构重排或整合到粟酒裂殖酵母中。从酿酒酵母转移到粟酒裂殖酵母后,端粒几乎没有生长。提出了一个模型来解释质粒的起源。