Busby S, Ebright R H
School of Biochemistry, University of Birmingham, UK.
Mol Microbiol. 1997 Mar;23(5):853-9. doi: 10.1046/j.1365-2958.1997.2771641.x.
Transcription activation at Class II CAP-dependent promoters provides a paradigm for understanding how a single activator molecule can make multiple interactions with the transcription machinery, with each interaction being responsible for a specific mechanistic consequence. At Class II CAP-dependent promoters, the DNA target site for CAP is centred near position -42, overlapping and replacing the -35 determinant for binding of RNA polymerase (RNAP). Transcription activation requires two distinct mechanistic components. The first component is 'anti-inhibition,' overcoming an inhibitory effect of the RNAP alpha subunit C-terminal domain (alpha CTD). This component involves direct contact between amino acids 156-164 (activating region 1) of the upstream subunit of the CAP dimer and a target in alpha CTD. The second component is 'direct activation', facilitating isomerization of the RNAP-promoter closed complex to the transcriptionally competent open complex. This component involves direct contact between amino acids 19, 21 and 101 (activating region 2) of the downstream subunit of the CAP dimer and a target in the RNAP alpha subunit N-terminal domain (alpha NTD).
II类CAP依赖性启动子的转录激活为理解单个激活分子如何与转录机制进行多种相互作用提供了一个范例,每种相互作用都导致特定的机制结果。在II类CAP依赖性启动子中,CAP的DNA靶位点位于-42位附近的中心位置,与RNA聚合酶(RNAP)结合的-35决定簇重叠并取代它。转录激活需要两个不同的机制组分。第一个组分是“抗抑制”,克服RNAP α亚基C末端结构域(α CTD)的抑制作用。该组分涉及CAP二聚体上游亚基的156 - 164位氨基酸(激活区域1)与α CTD中的一个靶点直接接触。第二个组分是“直接激活”,促进RNAP - 启动子闭合复合物向转录活性开放复合物的异构化。该组分涉及CAP二聚体下游亚基的19、21和101位氨基酸(激活区域2)与RNAP α亚基N末端结构域(α NTD)中的一个靶点直接接触。