Department of Bioengineering, University of California, San Diego, La Jolla, CA 92093, USA.
BMC Biol. 2014 Jan 24;12:4. doi: 10.1186/1741-7007-12-4.
At the beginning of the transcription process, the RNA polymerase (RNAP) core enzyme requires a σ-factor to recognize the genomic location at which the process initiates. Although the crucial role of σ-factors has long been appreciated and characterized for many individual promoters, we do not yet have a genome-scale assessment of their function.
Using multiple genome-scale measurements, we elucidated the network of σ-factor and promoter interactions in Escherichia coli. The reconstructed network includes 4,724 σ-factor-specific promoters corresponding to transcription units (TUs), representing an increase of more than 300% over what has been previously reported. The reconstructed network was used to investigate competition between alternative σ-factors (the σ70 and σ38 regulons), confirming the competition model of σ substitution and negative regulation by alternative σ-factors. Comparison with σ-factor binding in Klebsiella pneumoniae showed that transcriptional regulation of conserved genes in closely related species is unexpectedly divergent.
The reconstructed network reveals the regulatory complexity of the promoter architecture in prokaryotic genomes, and opens a path to the direct determination of the systems biology of their transcriptional regulatory networks.
在转录过程开始时,RNA 聚合酶(RNAP)核心酶需要一个σ因子来识别起始的基因组位置。尽管 σ 因子的关键作用早已被广泛认识和描述,但我们还没有对它们的功能进行全基因组评估。
我们使用多种全基因组测量方法,阐明了大肠杆菌中 σ 因子和启动子相互作用的网络。重建的网络包括 4724 个 σ 因子特异性启动子,对应于转录单位(TU),比以前报道的增加了 300%以上。重建的网络用于研究替代 σ 因子(σ70 和 σ38 调控子)之间的竞争,证实了 σ 替代的竞争模型和替代 σ 因子的负调控。与肺炎克雷伯氏菌中 σ 因子结合的比较表明,密切相关物种中保守基因的转录调控出乎意料地存在差异。
重建的网络揭示了原核基因组启动子结构的调控复杂性,并为直接确定其转录调控网络的系统生物学开辟了道路。