O'Rourke Sara M, Estell William, Scott William G
Department of Chemistry and Biochemistry and The Center for the Molecular Biology of RNA, University of California at Santa Cruz, Santa Cruz, CA 95064, USA.
Department of Chemistry and Biochemistry and The Center for the Molecular Biology of RNA, University of California at Santa Cruz, Santa Cruz, CA 95064, USA.
J Mol Biol. 2015 Jul 17;427(14):2340-7. doi: 10.1016/j.jmb.2015.05.005. Epub 2015 May 14.
We report here that a single additional trans-Hoogsteen base-pairing interaction in the minimal hammerhead ribozyme transforms an RNA sequence possessing typically modest catalytic activity into one possessing greatly enhanced catalytic activity that is instead typical of full-length natural hammerhead RNAs that have additional extensive tertiary contact interactions. Formation of this additional base-pairing interaction requires only that the substrate RNA sequence contains a U at a position seven nucleotides 3' to the cleavage site. No additions or changes are required in the minimal hammerhead ribozyme enzyme strand sequence (providing that the naturally occurring GUGA tetraloop of Stem II is maintained). This finding unambiguously demonstrates that a single Hoogsteen base-pairing interaction, in full-length hammerheads possessing this interaction, is sufficient for stabilizing the ribozyme active site, including alignment of the attacking nucleophile for the required inline hammerhead ribozyme reaction mechanism. This finding also implies that the idiosyncratic arrays of additional tertiary contacts observed in all naturally occurring full-length hammerhead sequences have evolved to prevent deleterious alternative pairing interactions within the context of the variety of natural sequences arising in vivo. Finally, this finding greatly simplifies and rationalizes the design of fast-cleaving engineered synthetic ribozymes as RNA nucleolytic reagents and as subjects for enzyme kinetics and mechanistic investigations.
我们在此报告,最小锤头状核酶中单一额外的反式Hoogsteen碱基配对相互作用,可将通常具有适度催化活性的RNA序列转化为具有大大增强的催化活性的序列,这种增强的催化活性反而典型地存在于具有额外广泛三级接触相互作用的全长天然锤头状RNA中。形成这种额外的碱基配对相互作用仅要求底物RNA序列在切割位点3'端七个核苷酸的位置含有一个U。在最小锤头状核酶酶链序列中无需添加或改变(前提是茎II天然存在的GUGA四环得以保留)。这一发现明确表明,在具有这种相互作用的全长锤头状核酶中,单一的Hoogsteen碱基配对相互作用足以稳定核酶活性位点,包括使参与所需的内型锤头状核酶反应机制的亲核攻击物排列整齐。这一发现还意味着,在所有天然存在的全长锤头状序列中观察到的额外三级接触的特殊排列方式,是为了在体内产生的各种天然序列的背景下防止有害的替代配对相互作用而进化形成的。最后,这一发现极大地简化并合理化了作为RNA核酸裂解试剂以及作为酶动力学和机制研究对象的快速切割工程合成核酶的设计。