Gunge N, Kitada K
Kumamoto Institute of Technology, Japan.
Eur J Epidemiol. 1988 Dec;4(4):409-14. doi: 10.1007/BF00146390.
Two new linear plasmids, pK192L (4.9 kb) and pK192S (2.4 kb), were isolated from a Kluyveromyces lactis killer strain carrying pGKL1 and pGKL2. pK192L was a deletion plasmid of pGKL1, derived from a part of the ORF1, and had a palindrome structure of a 215 bp unique sequence flanked by 2.35 bp inverted repeats. pK192S was a hairpin plasmid produced by self-annealing of a single-stranded pK192L DNA. In genetic analysis, pK192L and pK192S always coexisted and replicated in cells harboring pGKL2 and pGKL1, in contrast to other pGKL1-derived deletion plasmids, such as F1, F2 and pGKLIS, which could replicate in cells carrying pGKL2 only. Based on these and other lines of evidence, it was concluded that the reason for the pGKL1 dependent replication of the pK192L/S plasmids was the absence of the intact pGKL1-ORF1 gene and that the ORF1 function was necessary for the replication of the pGKL1 genome. This finding is in good agreement with a recent view reporting that ORF1 may encode a DNA polymerase of pGKL1. In a separate experiment, four new linear plasmids were isolated from a Saccharomyces cerevisiae strain carrying pGKL1 and pGKL2. Structural analysis showed that they consisted of two pairs of hairpin-palindrome type plasmids, each derived from different parts of pGKL2, respectively. pGKL1 stability replicated in cells carrying both these pGKL2 derived deletion plasmids.
从携带pGKL1和pGKL2的乳酸克鲁维酵母杀伤菌株中分离出两个新的线性质粒,pK192L(4.9 kb)和pK192S(2.4 kb)。pK192L是pGKL1的缺失质粒,源自ORF1的一部分,具有由2.35 bp反向重复序列侧翼的215 bp独特序列的回文结构。pK192S是由单链pK192L DNA自退火产生的发夹质粒。在遗传分析中,与其他源自pGKL1的缺失质粒(如F1、F2和pGKLIS,它们只能在携带pGKL2的细胞中复制)不同,pK192L和pK192S总是在携带pGKL2和pGKL1的细胞中共存并复制。基于这些及其他证据,得出结论:pK192L/S质粒依赖pGKL1复制的原因是缺乏完整的pGKL1-ORF1基因,且ORF1功能对于pGKL1基因组的复制是必需的。这一发现与最近报道ORF1可能编码pGKL1的DNA聚合酶的观点高度一致。在另一个实验中,从携带pGKL1和pGKL2的酿酒酵母菌株中分离出四个新的线性质粒。结构分析表明,它们由两对发夹-回文型质粒组成,分别源自pGKL2的不同部分。pGKL1在携带这两种源自pGKL2的缺失质粒的细胞中稳定复制。