Truncaite Lidija, Zajanckauskaite Aurelija, Nivinskas Rimas
Laboratory of Gene Engineering, Institute of Biochemistry, Vilnius, Lithuania.
J Mol Biol. 2002 Mar 22;317(2):179-90. doi: 10.1006/jmbi.2002.5407.
Bacteriophage T4 DNA ligase gene 30 lies in the cluster of prereplicative genes located counterclockwise from map units 149 to 121. Based on the early transcription studies this gene has been considered as a typical early gene of bacteriophage T4. In agreement with this assignment, two strong T4 early promoters, P(E )30.8 (128.6) and P(E )30.7 (128.2), located about 3.1 and 2.7 kb upstream from gene 30 have been revealed by promoter mapping and sequence analysis. In addition, the existence of a putative early promoter just upstream of gene 30 was proposed from the sequence data. However, here we show that the putative early promoter just upstream of gene 30 is, in fact, a T4 middle promoter. Furthermore, we detected one more middle promoter located in the genomic region between early promoter P(E )30.7 (128.2) and DNA ligase gene 30 in the coding region of gene 30.3. Both new middle promoters have differences from the consensus MotA box, while their -10 regions match the sigma(70) consensus sequence very well. The 5' ends of MotA-dependent transcripts directed from these promoters, as well as the kinetics of 5' end accumulation in the cells, have been determined by primer extension analysis. The results of these analyses indicate that both MotA-dependent and MotA-independent promoters control the transcription of T4 DNA ligase gene 30 in vivo. Moreover, we show that the first transcripts for gene 30 are directed from its own middle promoter, P(M)30.
噬菌体T4 DNA连接酶基因30位于复制前基因簇中,该基因簇从图谱单位149逆时针排列至121。基于早期转录研究,该基因被认为是噬菌体T4的典型早期基因。与这一归属一致,通过启动子定位和序列分析发现了两个强有力的T4早期启动子,P(E)30.8(128.6)和P(E)30.7(128.2),它们位于基因30上游约3.1 kb和2.7 kb处。此外,从序列数据推测基因30上游存在一个假定的早期启动子。然而,我们在此表明,基因30上游的假定早期启动子实际上是一个T4中期启动子。此外,我们在基因30.3的编码区中,早期启动子P(E)30.7(128.2)和DNA连接酶基因30之间的基因组区域检测到另一个中期启动子。这两个新的中期启动子与共有MotA框存在差异,而它们的-10区与sigma(70)共有序列匹配得非常好。通过引物延伸分析确定了从这些启动子起始的MotA依赖性转录本的5'末端,以及细胞中5'末端积累的动力学。这些分析结果表明,MotA依赖性和MotA非依赖性启动子在体内均控制噬菌体T4 DNA连接酶基因30的转录。此外,我们表明基因30的首批转录本来自其自身的中期启动子P(M)30。