Cox E C, Horner D L
J Mol Biol. 1986 Jul 5;190(1):113-7. doi: 10.1016/0022-2836(86)90080-x.
The mutD(dnaQ) gene in Escherichia coli codes for the epsilon subunit of the DNA polymerase pol III holoenzyme. Previous work has shown that this gene lies adjacent to the gene coding for RNase H (rnh). The two products are translated from diverging promoters. Here we report on the 1.6 kb (1 kb = 10(3) bases or base-pairs) sequence of the region coding for both genes, and the transcripts encoded by them. mutD codes for two transcripts, one of whose origins lies within the rnh structural gene. Both transcripts overlap and are complementary to a region of the rnh transcript. Thus, they can potentially form double-stranded helices with rnh. Of the two possible double-stranded structures, the shorter does not interfere with a likely rnh ribosome binding site, while the longer one does. We suggest that this unique organization may regulate rnh translation rates.
大肠杆菌中的mutD(dnaQ)基因编码DNA聚合酶III全酶的ε亚基。先前的研究表明,该基因与编码核糖核酸酶H(rnh)的基因相邻。这两种产物由不同的启动子转录。在此,我们报告了编码这两个基因的区域的1.6 kb(1 kb = 10³个碱基或碱基对)序列以及它们所编码的转录本。mutD编码两种转录本,其中一种的起始位点位于rnh结构基因内。两种转录本相互重叠,并且与rnh转录本的一个区域互补。因此,它们有可能与rnh形成双链螺旋。在两种可能的双链结构中,较短的一种不会干扰rnh可能的核糖体结合位点,而较长的一种则会。我们认为这种独特的结构可能会调节rnh的翻译速率。