Mysiak Monika E, Bleijenberg Marjoleine H, Wyman Claire, Holthuizen P Elly, van der Vliet Peter C
Department of Physiological Chemistry, University Medical Center Utrecht, and Centre for Biomedical Genetics, 3584 CG Utrecht, The Netherlands.
J Virol. 2004 Feb;78(4):1928-35. doi: 10.1128/jvi.78.4.1928-1935.2004.
Nuclear factor I (NFI) is a transcription factor that binds to the adenovirus type 5 (Ad5) origin of replication and recruits the adenovirus DNA polymerase, thereby stimulating initiation of DNA replication in vitro. Using scanning force microscopy, we demonstrate that NFI induces a 60 degrees bend upon binding to the origin. The A/T-rich region preceding the core recognition sequence of NFI influences the DNA bend angle, since substitution of A/T base pairs by G/C base pairs severely decreases bending. Mutations in the A/T-rich region do not affect binding of NFI to DNA. However, mutations that reduce the protein-induced bend lead to a loss of NFI-stimulated replication, indicating that DNA bending is functionally important. In contrast, basal initiation or DNA binding of the polymerase is not impaired by these origin mutations. We conclude that binding of NFI to the Ad5 origin causes structural changes in DNA that are essential for the stimulatory function of NFI in replication. We propose that NFI-induced origin bending facilitates the assembly of a functional initiation complex.
核因子I(NFI)是一种转录因子,它能与5型腺病毒(Ad5)的复制起点结合,并募集腺病毒DNA聚合酶,从而在体外刺激DNA复制的起始。利用扫描力显微镜,我们证明NFI与起点结合时会诱导60度的弯曲。NFI核心识别序列之前富含A/T的区域会影响DNA弯曲角度,因为用G/C碱基对替换A/T碱基对会严重降低弯曲程度。富含A/T区域的突变不影响NFI与DNA的结合。然而,减少蛋白质诱导弯曲的突变会导致NFI刺激的复制丧失,这表明DNA弯曲在功能上很重要。相比之下,这些起点突变不会损害聚合酶的基础起始或DNA结合。我们得出结论,NFI与Ad5起点的结合会导致DNA发生结构变化,这对于NFI在复制中的刺激功能至关重要。我们提出,NFI诱导的起点弯曲有助于功能性起始复合物的组装。