Polayes D A, Rice P W, Dahlberg J E
Department of Physiological Chemistry, University of Wisconsin, Madison 53706.
J Bacteriol. 1988 May;170(5):2083-8. doi: 10.1128/jb.170.5.2083-2088.1988.
We have shown that the level of DNA polymerase I (Pol I) activity in Escherichia coli is influenced by the level of a 109-nucleotide RNA, spot 42 RNA. Deletion of the gene for spot 42 RNA results in a 20 to 25% decrease in Pol I activity, as assayed by nucleotide incorporation in cell extracts and a decrease in the ability of cells to grow in the presence of the DNA-alkylating agent methyl methanesulfonate. Also, a physiological reduction of the level of spot 42 RNA, by growth in media containing poor carbon sources, results in a corresponding decrease in Pol I activity. Conversely, overproduction of spot 42 RNA results in a 10 to 15% increase in Pol I activity in vitro. Thus, changes in the amount of spot 42 RNA result in relatively small but significant changes in Pol I activity.
我们已经证明,大肠杆菌中DNA聚合酶I(Pol I)的活性水平受一种109个核苷酸的RNA即斑点42 RNA水平的影响。通过在细胞提取物中掺入核苷酸来测定,斑点42 RNA基因的缺失会导致Pol I活性降低20%至25%,并且细胞在DNA烷化剂甲磺酸甲酯存在下生长的能力也会下降。此外,通过在含有贫碳源的培养基中生长使斑点42 RNA水平发生生理性降低,会导致Pol I活性相应下降。相反,斑点42 RNA的过量产生会导致体外Pol I活性增加10%至15%。因此,斑点42 RNA量的变化会导致Pol I活性发生相对较小但显著的变化。