Gunge Norio, Takata Hideki, Matsuura Akira, Fukuda Kohsai
Molecular Genetics, Applied Microbial Technology, Sojo University. Ikeda 4-22-1, Kumamoto, 860-0082. Japan.
Biol Proced Online. 2003;5:29-42. doi: 10.1251/bpo44. Epub 2003 Feb 17.
Relocation into the nucleus of the yeast cytoplasmic linear plasmids was studied using a monitor plasmid pCLU1. In Saccharomyces cerevisiae, the nuclearly-relocated pCLU1 replicated in a linear form (termed pTLU-type plasmid) which carried the host telomeric repeats TG(1-3) of 300-350 bp at both ends. The telomere sequences mainly consisted of a major motif TGTGTGGGTGTGG which was complementary to part of the RNA template of yeast telomerase and were directly added to the very end of the pCLU1-terminal element ITR (inverted terminal repeat), suggesting that the ITR end played a role as a substrate of telomerase. The telomere sequences varied among isolated pTLU-type plasmids, but the TG(1-3) organization was symmetrically identical on both ends of any one plasmid. During cell growth under non-selective condition, the telomeric repeat sequences were progressively rearranged on one side, but not on the opposite side of pTLU plasmid ends. This indicates that the mode of telomeric DNA replication or repair differed between both ends. Clonal analysis showed that the intense rearrangement of telomeric DNA was closely associated with extreme instability of pTLU plasmids.
利用监测质粒pCLU1研究了酵母细胞质线性质粒向细胞核的转移。在酿酒酵母中,转移至细胞核的pCLU1以线性形式复制(称为pTLU型质粒),其两端携带300 - 350 bp的宿主端粒重复序列TG(1 - 3)。端粒序列主要由一个主要基序TGTGTGGGTGTGG组成,该基序与酵母端粒酶RNA模板的一部分互补,并直接添加到pCLU1末端元件ITR(反向末端重复序列)的最末端,这表明ITR末端起到了端粒酶底物的作用。在分离的pTLU型质粒中,端粒序列各不相同,但任何一个质粒两端的TG(1 - 3)结构都是对称相同的。在非选择性条件下的细胞生长过程中,端粒重复序列在pTLU质粒一端逐渐重排,但另一端则没有。这表明两端的端粒DNA复制或修复模式不同。克隆分析表明,端粒DNA的强烈重排与pTLU质粒的极端不稳定性密切相关。