Adley C C, Bukhari A I
Nucleic Acids Res. 1984 Apr 25;12(8):3535-50. doi: 10.1093/nar/12.8.3535.
The expression of the DNA modification gene (mom) of bacteriophage Mu requires the cellular deoxyadenosine methylase (dam) and a transactivation factor from the phage. By hypothesis, the transcription of mom is activated by methylation of three GATC sequences upstream from the mom gene. We have introduced small deletions at a fourth GATC site located about 140 base pairs downstream from the primary methylation region. Some of the deletions severely affect the mom gene expression. We propose from this analysis that (1) some important elements, possibly the promoter, concerned with the expression of mom are located between nucleotides 840 and 880 from the right end of Mu and (2) the mom protein starts with the codon GTG located at position 810. We favor the hypothesis that methylation turns off transcription upstream, thereby allowing the main mom promoter to function.
噬菌体Mu的DNA修饰基因(mom)的表达需要细胞脱氧腺苷甲基化酶(dam)和来自噬菌体的反式激活因子。根据假设,mom的转录是由mom基因上游三个GATC序列的甲基化激活的。我们在位于主要甲基化区域下游约140个碱基对处的第四个GATC位点引入了小的缺失。一些缺失严重影响mom基因的表达。我们从该分析中提出:(1)与mom表达相关的一些重要元件,可能是启动子,位于Mu右端核苷酸840至880之间;(2)mom蛋白起始于位于810位的密码子GTG。我们支持这样的假设,即甲基化关闭上游转录,从而使主要的mom启动子发挥作用。