Gringauz E, Orle K A, Waddell C S, Craig N L
Department of Genetics, University of California, Berkely 94720.
J Bacteriol. 1988 Jun;170(6):2832-40. doi: 10.1128/jb.170.6.2832-2840.1988.
Transposon Tn7 inserts at high frequency into a specific site in the Escherichia coli chromosome called attTn7. We show that the point of Tn7 insertion in attTn7 lies within the transcriptional terminator of the bacterial glmS gene. We have exploited the glmS transcription terminator to isolate mutants with altered sequences at the point of Tn7 insertion and have used these mutants to show that the nucleotide sequence at the point of Tn7 insertion is irrelevant to attTn7 target activity. Thus, the nucleotides which provide attTn7 target activity are distinct from the point of Tn7 insertion. We have also examined the effect of transcription on the capacity of attTn7 to act as a target for Tn7 transposition. Our results suggest that transcription of attTn7 does not modulate its Tn7 target activity.
转座子Tn7以高频插入大肠杆菌染色体中一个名为attTn7的特定位点。我们发现Tn7在attTn7中的插入位点位于细菌glmS基因的转录终止子内。我们利用glmS转录终止子分离出在Tn7插入位点处序列发生改变的突变体,并利用这些突变体表明Tn7插入位点处的核苷酸序列与attTn7的靶标活性无关。因此,赋予attTn7靶标活性的核苷酸与Tn7的插入位点不同。我们还研究了转录对attTn7作为Tn7转座靶标的能力的影响。我们的结果表明,attTn7的转录不会调节其Tn7靶标活性。