Løbner-Olesen Anders, Marinus Martin G, Hansen Flemming G
Department of Life Sciences and Chemistry, Roskilde University, DK-4000 Roskilde, Denmark.
Proc Natl Acad Sci U S A. 2003 Apr 15;100(8):4672-7. doi: 10.1073/pnas.0538053100. Epub 2003 Apr 7.
High-density oligonucleotide arrays were used to monitor global transcription patterns in Escherichia coli with various levels of Dam and SeqA proteins. Cells lacking Dam methyltransferase showed a modest increase in transcription of the genes belonging to the SOS regulon. Bacteria devoid of the SeqA protein, which preferentially binds hemimethylated DNA, were found to have a transcriptional profile almost identical to WT bacteria overexpressing Dam methyltransferase. The latter two strains differed from WT in two ways. First, the origin proximal genes were transcribed with increased frequency due to increased gene dosage. Second, chromosomal domains of high transcriptional activity alternate with regions of low activity, and our results indicate that the activity in each domain is modulated in the same way by SeqA deficiency or Dam overproduction. We suggest that the methylation status of the cell is an important factor in forming and/or maintaining chromosome structure.
高密度寡核苷酸阵列用于监测具有不同水平Dam和SeqA蛋白的大肠杆菌中的全局转录模式。缺乏Dam甲基转移酶的细胞中,属于SOS调节子的基因转录略有增加。缺乏优先结合半甲基化DNA的SeqA蛋白的细菌,其转录谱几乎与过表达Dam甲基转移酶的野生型细菌相同。后两种菌株与野生型在两个方面存在差异。首先,由于基因剂量增加,靠近复制起点的基因转录频率增加。其次,高转录活性的染色体结构域与低活性区域交替出现,我们的结果表明,SeqA缺陷或Dam过量产生以相同方式调节每个结构域的活性。我们认为细胞的甲基化状态是形成和/或维持染色体结构的重要因素。