Katayose Y, Kajiwara S, Shishido K
Department of Life Science, Faculty of Science, Tokyo Institute of Technology, Yokohama, Japan.
Nucleic Acids Res. 1990 Mar 25;18(6):1395-400. doi: 10.1093/nar/18.6.1395.
A linear DNA plasmid, designated pLLE1, has been isolated from a mitochondrial fraction of a strain of Lentinus edodes. pLLE1(11.0 kbp) was sensitive to the 3'----5'-acting exonuclease III and resistant to the 5'----3'-acting lambda exonuclease. It showed no homology with mitochondrial and nuclear genomic DNAs of plasmidless strain as well as the pLLE1-harboring host strain of L. edodes. The 1434-bp fragment (sequences) capable of autonomous replication in the yeast Saccharomyces cerevisiae (ARSs) was cloned from pLLE1 DNA with YIp32 (pBR322 containing yeast LEU2 DNA), which displayed a high ARS activity. The cloned 1434-bp fragment was shown to lie near to the end of pLLE1 DNA (nucleotides about 800-2200) and contained three consecutive ARS consensus sequences (A/T)TTTAT(A/G)TTT(A/T) of S. cerevisiae and dispersive eight ARS consensus-like sequences. The subcloned 366-bp fragment containing the three ARSs retained original ARS activity of the 1434-bp fragment.
一种名为pLLE1的线性DNA质粒已从香菇菌株的线粒体组分中分离出来。pLLE1(11.0 kbp)对3'→5'作用的核酸外切酶III敏感,对5'→3'作用的λ核酸外切酶具有抗性。它与无质粒菌株以及携带pLLE1的香菇宿主菌株的线粒体和核基因组DNA均无同源性。利用YIp32(含有酵母LEU2 DNA的pBR322)从pLLE1 DNA中克隆出了能够在酿酒酵母中自主复制的1434 bp片段(序列)(ARSs),该片段显示出高ARS活性。克隆的1434 bp片段位于pLLE1 DNA末端附近(核苷酸约800 - 2200),包含三个连续的酿酒酵母ARS共有序列(A/T)TTTAT(A/G)TTT(A/T)和分散的八个ARS共有样序列。包含这三个ARS的亚克隆366 bp片段保留了1434 bp片段的原始ARS活性。