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利用具有益生元合理性的核糖核苷2',3'-环磷酸对RNA进行非经典3'-5'延伸。

Non-canonical 3'-5' extension of RNA with prebiotically plausible ribonucleoside 2',3'-cyclic phosphates.

作者信息

Mutschler Hannes, Holliger Philipp

机构信息

MRC Laboratory of Molecular Biology, Cambridge Biomedical Campus , Francis Crick Avenue, Cambridge CB2 0QH, United Kingdom.

出版信息

J Am Chem Soc. 2014 Apr 9;136(14):5193-6. doi: 10.1021/ja4127714. Epub 2014 Mar 28.

Abstract

Ribonucleoside 2',3'-cyclic phosphates (N>p's) are generated by multiple prebiotically plausible processes and are credible building blocks for the assembly of early RNA oligomers. While N>p's can be polymerized into short RNAs by non-enzymatic processes with variable efficiency and regioselectivity, no enzymatic route for RNA synthesis had been described. Here we report such a non-canonical 3'-5' nucleotidyl transferase activity. We engineered a variant of the hairpin ribozyme to catalyze addition of all four N>p's (2',3'-cyclic A-, G-, U-, and CMP) to the 5'-hydroxyl termini of RNA strands with 5' nucleotide addition enhanced in all cases by eutectic ice phase formation at -7 °C. We also observed 5' addition of 2',3'-cyclic phosphate-activated β-nicotinamide adenine dinucleotide (NAD>p) and ACA>p RNA trinucleotide, and multiple additions of GUCCA>p RNA pentamers. Our results establish a new mode of RNA 3'-5' extension with implications for RNA oligomer synthesis from prebiotic nucleotide pools.

摘要

核糖核苷2',3'-环磷酸酯(N>p's)可通过多种在生命起源前看似合理的过程生成,并且是早期RNA寡聚物组装的可信构件。虽然N>p's可以通过非酶促过程以可变的效率和区域选择性聚合成短RNA,但尚未描述RNA合成的酶促途径。在这里,我们报告了这样一种非经典的3'-5'核苷酸转移酶活性。我们设计了一种发夹状核酶变体,以催化将所有四种N>p's(2',3'-环A-、G-、U-和CMP)添加到RNA链的5'-羟基末端,在所有情况下,通过在-7°C形成共晶冰相,5'核苷酸添加都得到增强。我们还观察到2',3'-环磷酸酯激活的β-烟酰胺腺嘌呤二核苷酸(NAD>p)和ACA>p RNA三核苷酸的5'添加,以及GUCCA>p RNA五聚体的多次添加。我们的结果建立了一种新的RNA 3'-5'延伸模式,对从生命起源前的核苷酸库合成RNA寡聚物具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49a6/4333585/16907dcd92f4/ja-2013-127714_0001.jpg

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