Fabozzi G, Paolozzi L, Ghelardini P
Centro Studi per gli Acidi Nucleici del CNR, Rome, Italy.
Virology. 1998 Feb 1;241(1):73-9. doi: 10.1006/viro.1997.8948.
The gem operon of bacteriophage Mu, responsible for the complex phenomenon of phage conversion, is included in the so called "semiessential early" region of phage DNA. Unlike the other early genes of the phage which are transcribed from the pe promoter, expression of the gem operon is driven by its own promoter, which escapes the control of the repressor. In fact, the transcript corresponding to gem was detected in immune lysogens by using a combined reverse transcription and a subsequent amplification of the resulting cDNA. The transcription initiation site from pgem was determined by primer extension mapping experiments and localized at 8217 bp from the left end of phage DNA. Two elements which could perform the negative control of gem were also identified. The first is a phage product, GemB, which presumably interferes with gem expression at a posttranscriptional level, whereas the second is a structural element, an inverted repeat immediately downstream of pgem, which acts as a terminator for the transcripts starting from pe. These transcripts could regulate gem expression by interfering with the initiation of transcription from pgem.
噬菌体Mu的gem操纵子负责噬菌体转化这一复杂现象,它包含在噬菌体DNA的所谓“半必需早期”区域。与噬菌体其他从pe启动子转录的早期基因不同,gem操纵子的表达由其自身的启动子驱动,该启动子不受阻遏物的控制。事实上,通过结合逆转录和对所得cDNA的后续扩增,在免疫溶原菌中检测到了与gem对应的转录本。通过引物延伸定位实验确定了pgem的转录起始位点,并将其定位在距噬菌体DNA左端8217 bp处。还鉴定出了两个可对gem进行负调控的元件。第一个是噬菌体产物GemB,它可能在转录后水平干扰gem的表达,而第二个是一个结构元件,即pgem下游紧邻的一个反向重复序列,它作为从pe起始的转录本的终止子。这些转录本可能通过干扰从pgem起始的转录来调节gem的表达。