Cesareni G, Muesing M A, Polisky B
Proc Natl Acad Sci U S A. 1982 Oct;79(20):6313-7. doi: 10.1073/pnas.79.20.6313.
A 600-base-pair region essential for ColE1 and pMBl plasmid replication contains two promoters responsible for the synthesis of two RNA molecules central to copy number control. One promoter directs synthesis of the primer RNA precursor. The second promoter directs the synthesis of a small RNA molecule, RNAl, which acts in trans to inhibit processing of the RNA primer precursor. We have fused each promoter to the beta-galactosidase structural gene contained in a lambda phage. Expression of the RNAl promoter in lysogens is not influenced by the presence of wild-type pMBl or ColEl plasmids residing in the cell. Transcription from the RNA primer promoter, however, is repressed by the product of a trans-acting plasmid gene product, which we have designated rop (for repressor of primer). The rop gene maps downstream from the replication origin in a region that encodes a polypeptide of 63 amino acids whose sequence is completely conserved in pMBl and ColE1. We propose that this polypeptide is the rop gene product and that it regulates plasmid DNA replication by modulating the initiation of transcription of the primer RNA precursor.
对ColE1和pMBl质粒复制至关重要的一个600个碱基对的区域包含两个启动子,它们负责合成两个对拷贝数控制至关重要的RNA分子。一个启动子指导引物RNA前体的合成。第二个启动子指导一个小RNA分子RNA1的合成,RNA1通过反式作用抑制RNA引物前体的加工。我们已将每个启动子与λ噬菌体中包含的β-半乳糖苷酶结构基因融合。溶原菌中RNA1启动子的表达不受细胞中野生型pMBl或ColE1质粒存在的影响。然而,RNA引物启动子的转录受到一个反式作用质粒基因产物的抑制,我们将其命名为rop(引物阻遏物)。rop基因定位于复制起点下游的一个区域,该区域编码一个63个氨基酸的多肽,其序列在pMBl和ColE1中完全保守。我们推测这个多肽是rop基因产物,并且它通过调节引物RNA前体转录的起始来调控质粒DNA复制。