Praszkier J, Bird P, Nikoletti S, Pittard J
Department of Microbiology, University of Melbourne, Parkville, Victoria, Australia.
J Bacteriol. 1989 Sep;171(9):5056-64. doi: 10.1128/jb.171.9.5056-5064.1989.
Transcriptional mapping studies of the IncB minireplicon pMU720 demonstrated the existence of a long RNA molecule, RNA II, whose 5' portion is complementary to the product of the incompatibility gene RNA I. By using gene fusion and transcriptional fusion plasmids, it was shown that RNA I regulated the expression of the RNA II gene product and that it did so primarily at the level of translation. The target of RNA I was mapped to lie within a 216-base region of RNA II containing the sequence complementary to RNA I. Introduction of the target for RNA I in trans increased the copy number of an IncB minireplicon, indicating that RNA I and RNA II form the basis of the copy number control system of IncB plasmids.
对IncB微型复制子pMU720的转录图谱研究表明,存在一种长RNA分子,即RNA II,其5'部分与不相容性基因RNA I的产物互补。通过使用基因融合和转录融合质粒,结果显示RNA I调节RNA II基因产物的表达,并且主要是在翻译水平上进行调节。RNA I的靶标被定位在RNA II的一个216个碱基的区域内,该区域包含与RNA I互补的序列。反式引入RNA I的靶标增加了IncB微型复制子的拷贝数,这表明RNA I和RNA II构成了IncB质粒拷贝数控制系统的基础。