Todd Alan K, Haider Shozeb M, Parkinson Gary N, Neidle Stephen
Cancer Research UK Biomolecular Structure Group, The School of Pharmacy, University of London, 29-39 Brunswick Square, London WC1N 1AX, UK.
Nucleic Acids Res. 2007;35(17):5799-808. doi: 10.1093/nar/gkm609. Epub 2007 Aug 24.
The 22-nt c-kit87 promoter sequence is unique within the human genome. Its fold and tertiary structure have recently been determined by NMR methods [Phan,A.T., Kuryavyi,V., Burge,S., Neidle,S. and Patel,D.J. (2007) Structure of an unprecedented G-quadruplex scaffold in the c-kit promoter. J. Am. Chem. Soc., 129, 4386-4392], and does not have precedent among known DNA quadruplexes. We show here using bioinformatics and molecular dynamics simulations methods that (i) none of the closely related sequences (encompassing all nucleotides not involved in the maintenance of structural integrity) occur immediately upstream (<100 nt) of a transcription start site, and (ii) that all of these sequences correspond to the same stable tertiary structure. It is concluded that the c-kit87 tertiary structure may also be formed in a very small number of other loci in the human genome, but the likelihood of these playing a significant role in the expression of particular genes is very low. The c-kit87 quadruplex thus fulfils a fundamental criterion of a 'good' drug target, in that it possesses distinctive three-dimensional structural features that are only present in at most a handful of other genes.
22个核苷酸的c-kit87启动子序列在人类基因组中是独一无二的。其折叠和三级结构最近已通过核磁共振方法确定[Phan, A.T., Kuryavyi, V., Burge, S., Neidle, S. 和Patel, D.J. (2007) c-kit启动子中前所未有的G-四链体支架结构。《美国化学会志》,129, 4386 - 4392],在已知的DNA四链体中没有先例。我们在此使用生物信息学和分子动力学模拟方法表明:(i) 所有密切相关序列(包含所有不参与维持结构完整性的核苷酸)均未出现在转录起始位点上游紧邻区域(<100个核苷酸);(ii) 所有这些序列都对应于相同的稳定三级结构。得出的结论是,c-kit87三级结构可能也会在人类基因组中极少数其他位点形成,但这些位点在特定基因表达中发挥重要作用的可能性非常低。因此,c-kit87四链体满足了一个“良好”药物靶点的基本标准,即它具有独特的三维结构特征,这些特征最多只存在于少数其他基因中。