Smits M A, Jansen J, Konings R N, Schoenmakers J G
Nucleic Acids Res. 1984 May 25;12(10):4071-81. doi: 10.1093/nar/12.10.4071.
Transcription of the infrequently expressed phage M13 genome domain, comprising genes III, VI, I and IV, has been studied in detail by hybridization and S1-nuclease mapping studies. The contiguous genes III and VI are transcribed via an 1800 nucleotide-long RNA molecule that is initiated at a promoter which overlaps with the Rho-independent termination signal between genes III and VIII. Its synthesis is terminated at a Rho-dependent terminator in the proximal part of gene I. Transcription of gene I is not mediated by an independent promoter but most probably by read-through of RNA-polymerase through this terminator. Transcription of gene IV is accomplished by synthesis of four distinct RNAs of about 1500 to 1680 nucleotides long which are initiated at a promoter located immediately in front of gene IV. Termination of these transcripts is generated at least four different sites located in tandem within the intergenic region between genes IV and II.
对噬菌体M13基因组中不常表达的区域(包含基因III、VI、I和IV)的转录,已通过杂交和S1核酸酶图谱分析研究进行了详细研究。相邻的基因III和VI通过一个1800个核苷酸长的RNA分子进行转录,该分子起始于一个启动子,该启动子与基因III和VIII之间的不依赖Rho的终止信号重叠。其合成在基因I近端的一个依赖Rho的终止子处终止。基因I的转录不是由独立启动子介导的,很可能是RNA聚合酶通过这个终止子通读实现的。基因IV的转录是通过合成四种不同的约1500至1680个核苷酸长的RNA来完成的,这些RNA起始于基因IV正前方的一个启动子。这些转录本的终止至少发生在基因IV和II之间基因间区域内串联排列的四个不同位点。