Wade Joseph T, Castro Roa Daniel, Grainger David C, Hurd Douglas, Busby Stephen J W, Struhl Kevin, Nudler Evgeny
Department of Biological Chemistry and Molecular Pharmacology, Harvard University, Boston, Massachusetts 02115, USA.
Nat Struct Mol Biol. 2006 Sep;13(9):806-14. doi: 10.1038/nsmb1130. Epub 2006 Aug 6.
Bacterial core RNA polymerase (RNAP) must associate with a sigma factor to recognize promoter sequences. Escherichia coli encodes seven sigma factors, each believed to be specific for a largely distinct subset of promoters. Using microarrays representing the entire E. coli genome, we identify 87 in vivo targets of sigma32, the heat-shock sigma factor, and estimate that there are 120-150 sigma32 promoters in total. Unexpectedly, 25% of these sigma32 targets are located within coding regions, suggesting novel regulatory roles for sigma32. The majority of sigma32 promoter targets overlap with those of sigma70, the housekeeping sigma factor. Furthermore, their DNA sequence motifs are often interdigitated, with RNAPsigma70 and RNAPsigma32 initiating transcription in vitro with similar efficiency and from identical positions. SigmaE-regulated promoters also overlap extensively with those for sigma70. These results suggest that extensive functional overlap between sigma factors is an important phenomenon.
细菌核心RNA聚合酶(RNAP)必须与一个σ因子结合才能识别启动子序列。大肠杆菌编码七种σ因子,每种σ因子被认为主要特异性识别不同的启动子子集。利用代表整个大肠杆菌基因组的微阵列,我们鉴定出热休克σ因子σ32在体内的87个靶标,并估计总共有120 - 150个σ32启动子。出乎意料的是,这些σ32靶标中有25%位于编码区内,这表明σ32具有新的调控作用。大多数σ32启动子靶标与管家σ因子σ70的靶标重叠。此外,它们的DNA序列基序常常相互交错,RNAPσ70和RNAPσ32在体外以相似的效率并从相同位置起始转录。σE调控的启动子也与σ70的启动子广泛重叠。这些结果表明,σ因子之间广泛的功能重叠是一个重要现象。