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‘Z-DNA like’ fragments in RNA: a recurring structural motif with implications for folding RNA/protein recognition and immune response

机译:RNA中的 Z-DNA样片段:重复出现的结构基序可影响折叠RNA /蛋白质识别和免疫反应

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摘要

Since the work of Alexander Rich, who solved the first Z-DNA crystal structure, we have known that d(CpG) steps can adopt a particular structure that leads to forming left-handed helices. However, it is still largely unrecognized that other sequences can adopt ‘left-handed’ conformations in DNA and RNA, in double as well as single stranded contexts. These ‘Z-like’ steps involve the coexistence of several rare structural features: a C2’-endo puckering, a syn nucleotide and a lone pair–π stacking between a ribose O4’ atom and a nucleobase. This particular arrangement induces a conformational stress in the RNA backbone, which limits the occurrence of Z-like steps to ≈0.1% of all dinucleotide steps in the PDB. Here, we report over 600 instances of Z-like steps, which are located within r(UNCG) tetraloops but also in small and large RNAs including riboswitches, ribozymes and ribosomes. Given their complexity, Z-like steps are probably associated with slow folding kinetics and once formed could lock a fold through the formation of unique long-range contacts. Proteins involved in immunologic response also specifically recognize/induce these peculiar folds. Thus, characterizing the conformational features of these motifs could be a key to understanding the immune response at a structural level.
机译:自从亚历山大·里奇(Alexander Rich)解决了第一个Z-DNA晶体结构以来,我们就知道d(CpG)步骤可以采用导致形成左手螺旋的特殊结构。但是,人们仍然普遍不认识到其他序列在双链和单链情况下都可以采用DNA和RNA中的“左手”构象。这些“ Z形”步骤涉及几种罕见的结构特征的共存:C2'-内折叠,同义核苷酸和孤对-π堆叠在核糖O4'原子与核碱基之间。这种特殊的排列方式会在RNA主链中诱导构象应力,从而将Z样步骤的发生限制为PDB中所有二核苷酸步骤的≈0.1%。在这里,我们报告了600多个Z样步骤的实例,它们位于r(UNCG)四环内,也存在于大小RNA中,包括核糖开关,核酶和核糖体。鉴于它们的复杂性,Z形台阶可能与缓慢的折叠动力学相关联,一旦形成,就可以通过形成独特的远距离接触而锁定折叠。参与免疫应答的蛋白质也可以特异性识别/诱导这些特殊的折叠。因此,表征这些基序的构象特征可能是在结构水平上理解免疫反应的关键。

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