Marilley Monique, Milani Pascale, Thimonier Jean, Rocca-Serra José, Baldacci Giuseppe
Régulation génique et fonctionnelle & microscopie champ proche, EA 3290, IFR 125, Faculté de Médecine, Université de la Méditerranée, 27 Bd Jean Moulin, 13385 Marseille cedex 5, France.
Nucleic Acids Res. 2007;35(20):6832-45. doi: 10.1093/nar/gkm733. Epub 2007 Oct 11.
The replication origins (ORIs) of Schizosaccharomyces pombe, like those in most eukaryotes, are long chromosomal regions localized within A+T-rich domains. Although there is no consensus sequence, the interacting proteins are strongly conserved, suggesting that DNA structure is important for ORI function. We used atomic force microscopy in solution and DNA modelling to study the structural properties of the Spars1 origin. We show that this segment is the least stable of the surrounding DNA (9 kb), and contains regions of intrinsically bent elements (strongly curved and inherently supercoiled DNAs). The pORC-binding site co-maps with a superhelical DNA region, where the spatial arrangement of adenine/thymine stretches may provide the binding substrate. The replication initiation site (RIP) is located within a strongly curved DNA region. On pORC unwinding, this site shifts towards the apex of the curvature, thus potentiating DNA melting there. Our model is entirely consistent with the sequence variability, large size and A+T-richness of ORIs, and also accounts for the multistep nature of the initiation process, the specificity of pORC-binding site(s), and the specific location of RIP. We show that the particular DNA features and dynamic properties identified in Spars1 are present in other eukaryotic origins.
与大多数真核生物一样,粟酒裂殖酵母的复制起点(ORIs)是位于富含A+T结构域内的长染色体区域。尽管没有一致序列,但相互作用的蛋白质高度保守,这表明DNA结构对ORI功能很重要。我们使用溶液中的原子力显微镜和DNA建模来研究Spars1起点的结构特性。我们发现,该片段是周围DNA(9 kb)中最不稳定的部分,并且包含固有弯曲元件区域(强弯曲和固有超螺旋DNA)。pORC结合位点与一个超螺旋DNA区域共定位,其中腺嘌呤/胸腺嘧啶延伸的空间排列可能提供结合底物。复制起始位点(RIP)位于一个强弯曲的DNA区域内。在pORC解旋时,该位点向曲率顶点移动,从而增强那里的DNA解链。我们的模型与ORIs的序列变异性、大尺寸和富含A+T的特性完全一致,也解释了起始过程的多步性质、pORC结合位点的特异性以及RIP的特定位置。我们表明,在Spars1中鉴定出的特定DNA特征和动态特性也存在于其他真核生物的起点中。