Yoshimura H, Ikeda Y, Yoshimoto M, Tamaki S, Hanada K, Kusano T, Kohda T, Saito H, Oishi M
Taisho Pharmaceutical Co., Ltd, Saitama, Japan.
Nucleic Acids Res. 1991 Jul 11;19(13):3633-9. doi: 10.1093/nar/19.13.3633.
L factor is a unique plasmid DNA which was originally discovered in a subclone (B822) of mouse L cells at a high copy number (more than 5,000 copies/cell). The presence of L factor caused no detectable abnormalities to the plasmid-bearing cells. We determined the total DNA sequence of the L factor I (and a part of L factor II) and compared it with that of polyoma DNA. Both DNA are common to the general construction of DNA frames such as early, late and noncoding regions, suggesting the two to be closely related. On the other hand, the L factor DNA sequences differ substantially from that of polyoma in the DNA sequences corresponding to the polyoma large T antigen, capsid proteins and a portion of the enhancer region. In order to investigate the mechanism of plasmid establishment of L factor, we compared the enhancer activity, capacity of DNA replication and efficiency of plasmid establishment of L factor with those of polyoma. The results indicate that L factor enhancer activity and DNA replication capacity were considerably lower than those of polyoma, suggesting that these altered (lowered) activities associated with L factor contribute to the plasmidal establishment and stable maintenance of L factor.
L因子是一种独特的质粒DNA,最初是在小鼠L细胞的一个亚克隆(B822)中以高拷贝数(超过5000个拷贝/细胞)被发现的。L因子的存在对携带质粒的细胞没有可检测到的异常影响。我们测定了L因子I(以及L因子II的一部分)的全DNA序列,并将其与多瘤病毒DNA的序列进行了比较。两种DNA在DNA框架的一般构建方面是相同的,如早期、晚期和非编码区,这表明两者密切相关。另一方面,L因子的DNA序列在与多瘤病毒大T抗原、衣壳蛋白以及增强子区域的一部分相对应的DNA序列上与多瘤病毒有很大差异。为了研究L因子质粒建立的机制,我们将L因子的增强子活性、DNA复制能力和质粒建立效率与多瘤病毒的进行了比较。结果表明,L因子的增强子活性和DNA复制能力明显低于多瘤病毒,这表明与L因子相关的这些改变(降低)的活性有助于L因子的质粒建立和稳定维持。