Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA, 92037, USA.
NSF/NASA Center for Chemical Evolution, Atlanta, GA, 30332, USA.
Chemistry. 2018 Sep 3;24(49):12811-12819. doi: 10.1002/chem.201802287. Epub 2018 Aug 10.
The paradigm of homogenous-sugar-backbone of RNA and DNA has reliably guided the construction of many functional and useful xeno nucleic acid (XNA) systems to date. Deviations from this monotonous and canonical design, in many cases, results in oligonucleotide systems that lack base pairing with themselves, or with RNA or DNA. Here we show that nucleotides of two such compromised XNA systems can be combined with RNA and DNA in specific patterns to produce chimeric-backbone oligonucleotides, which in certain cases demonstrate base pairing properties comparable to-or stronger than-canonical systems, while also altering the conventional Watson-Crick pairing behavior. The unorthodox pairing properties generated from these chimeric sugar-backbone oligonucleotides suggest a counterintuitive approach of creating modules consisting of non-base pairing XNAs with RNA/DNA in a set pattern. This strategy has the potential to increase the diversity of unconventional nucleic acids leading to orthogonal backbone-sequence-controlled informational systems.
迄今为止,RNA 和 DNA 均为同型糖骨架的范例可靠地指导了许多功能和有用的异源核酸 (XNA) 系统的构建。在许多情况下,偏离这种单调且规范的设计会导致寡核苷酸系统自身或与 RNA 或 DNA 之间缺乏碱基配对。在这里,我们表明,两种此类受损 XNA 系统的核苷酸可以与 RNA 和 DNA 以特定模式组合,产生杂合骨架寡核苷酸,在某些情况下,其碱基配对性质可与规范系统相当,甚至更强,同时还改变了常规的 Watson-Crick 配对行为。这些杂合糖骨架寡核苷酸产生的非常规配对特性表明,采用一种反直觉的方法来创建由非碱基配对 XNAs 与 RNA/DNA 按照一定模式组成的模块。该策略有可能增加非常规核酸的多样性,从而形成正交骨架序列控制的信息系统。