Rojo F, Salas M
Centro de Biología Molecular (CSIC-UAM), Universidad Autónoma, Madrid, Spain.
EMBO J. 1991 Nov;10(11):3429-38. doi: 10.1002/j.1460-2075.1991.tb04907.x.
Binding of phage phi 29 regulatory protein p4 to its target sequences produces a strong bend in the DNA that is important for activation of the late A3 promoter (PA3). Protein p4 binding site in PA3 overlaps with the divergently transcribed main early promoter. PA2b, which suggested that p4 could also act as a repressor. We show that protein p4 both excludes Bacillus subtilis sigma A-RNA polymerase from PA2b and directs it to the divergently transcribed A3 promoter. Although steric hindrance is likely to be involved in the repression process, we have also analysed the effect on PA2b activity of a sequence-dependent curvature that simulates that induced by protein p4. A progressive increase in the DNA curvature of protein p4 binding region, performed by site-directed mutagenesis, has indicated that a static DNA curvature by itself can inhibit transcription from PA2b, both by impairing the binding of sigma A-RNA polymerase to the promoter and by reducing its ability to form transcriptionally active open complexes. These results indicate that bending promoter sequences in a direction unfavourable for RNA polymerase binding can repress transcription. Protein p4-induced DNA bending could therefore participate in PA2b repression by producing a DNA structure not recognized as a promoter by sigma A-RNA polymerase.
噬菌体phi 29调控蛋白p4与其靶序列的结合会使DNA产生强烈弯曲,这对晚期A3启动子(PA3)的激活很重要。PA3中的蛋白p4结合位点与反向转录的主要早期启动子重叠。PA2b表明p4也可能作为一种阻遏物。我们发现蛋白p4既阻止枯草芽孢杆菌σA-RNA聚合酶与PA2b结合,又将其导向反向转录的A3启动子。尽管空间位阻可能参与了阻遏过程,但我们也分析了模拟蛋白p4诱导的序列依赖性曲率对PA2b活性的影响。通过定点诱变对蛋白p4结合区域的DNA曲率进行逐步增加,结果表明,静态的DNA曲率本身就可以抑制PA2b的转录,这既通过损害σA-RNA聚合酶与启动子的结合,也通过降低其形成转录活性开放复合物的能力来实现。这些结果表明,朝着不利于RNA聚合酶结合的方向弯曲启动子序列可以抑制转录。因此,蛋白p4诱导的DNA弯曲可能通过产生一种不被σA-RNA聚合酶识别为启动子的DNA结构来参与PA2b的阻遏。