Masters M, Colloms M D, Oliver I R, He L, Macnaughton E J, Charters Y
Institute of Cell & Molecular Biology, University of Edinburgh, United Kingdom.
J Bacteriol. 1993 Jul;175(14):4405-13. doi: 10.1128/jb.175.14.4405-4413.1993.
The pcnB gene product of Escherchia coli is required for copy number maintenance of plasmids related to ColE1 and also for that of the IncFII plasmid R1. Because PcnB is similar to the tRNA-binding protein tRNA nucleotidyltransferase, we have suggested that the protein would be required only for processes in which an RNA is a prominent regulatory component. This appears to be so; strains deleted for pcnB, although defective in ColE1 and R1 plasmid maintenance, maintain the iteron-regulated plasmids F and P1 normally. We also find that strains deleted for pcnB grow normally, demonstrating that PcnB has no essential cellular role under the conditions tested and suggesting that regulation by antisense RNAs similar to RNAI has no critical role in any essential host process. We confirm by immunological tests that PcnB is likely to be the commercially available enzyme poly(A) polymerase.
大肠杆菌的pcnB基因产物是维持与ColE1相关质粒以及IncFII质粒R1拷贝数所必需的。由于PcnB与tRNA结合蛋白tRNA核苷酸转移酶相似,我们曾提出该蛋白仅在RNA是主要调节成分的过程中才是必需的。情况似乎确实如此;缺失pcnB的菌株,尽管在ColE1和R1质粒维持方面存在缺陷,但能正常维持迭代子调控的质粒F和P1。我们还发现,缺失pcnB的菌株生长正常,这表明在测试条件下PcnB没有重要的细胞功能,也表明类似于RNAI的反义RNA调控在任何重要的宿主过程中都没有关键作用。我们通过免疫测试证实,PcnB可能就是市售的酶聚腺苷酸聚合酶。