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古代进化在核糖体RNA折叠上的印记

Imprint of Ancient Evolution on rRNA Folding.

作者信息

Lanier Kathryn A, Athavale Shreyas S, Petrov Anton S, Wartell Roger, Williams Loren Dean

机构信息

School of Chemistry and Biochemistry and ‡School of Biology, Georgia Institute of Technology , Atlanta, Georgia 30332-0400, United States.

出版信息

Biochemistry. 2016 Aug 23;55(33):4603-13. doi: 10.1021/acs.biochem.6b00168. Epub 2016 Aug 10.

Abstract

In a model describing the origin and evolution of the translation system, ribosomal RNA (rRNA) grew in size by accretion [Petrov, A. S., et al. (2015) History of the Ribosome and the Origin of Translation. Proc. Natl. Acad. Sci. U.S.A. 112, 15396-15401]. Large rRNAs were built up by iterative incorporation and encasement of small folded RNAs, in analogy with addition of new LEGOs onto the surface of a preexisting LEGO assembly. In this model, rRNA robustness in folding arises from inherited autonomy of local folding. We propose that rRNAs can be decomposed at various granularities, retaining folding mechanism and folding competence. To test these predictions, we disassembled Domain III of the large ribosomal subunit (LSU). We determined whether local rRNA structure, stability, and folding pathways are autonomous. Thermal melting, chemical footprinting, and circular dichroism were used to infer rules that govern folding of rRNA. We deconstructed Domain III of the LSU rRNA by mapping out its complex multistep melting pathway. We studied Domain III and two equal-size "sub-Domains" of Domain III. The combined results are consistent with a model in which melting transitions of Domain III are conserved upon cleavage into sub-Domains. Each of the eight melting transitions of Domain III corresponds in Tm and ΔH with a transition observed in one of the two isolated sub-Domains. The results support a model in which structure, stability, and folding mechanisms are dominated by local interactions and are unaffected by separation of the sub-Domains. Domain III rRNA is distinct from RNAs that form long-range cooperative interaction networks at early stages of folding or that do not fold reversibly.

摘要

在一个描述翻译系统起源和进化的模型中,核糖体RNA(rRNA)的大小通过积累而增加[彼得罗夫,A. S.等人(2015年)核糖体的历史与翻译的起源。《美国国家科学院院刊》112,15396 - 15401]。大的rRNA是通过小折叠RNA的迭代掺入和包裹而构建起来的,这类似于在预先存在的乐高组件表面添加新的乐高积木。在这个模型中,rRNA折叠的稳健性源于局部折叠的遗传自主性。我们提出rRNA可以在各种粒度下分解,同时保留折叠机制和折叠能力。为了检验这些预测,我们拆解了大核糖体亚基(LSU)的结构域III。我们确定了局部rRNA结构、稳定性和折叠途径是否具有自主性。利用热变性、化学足迹法和圆二色性来推断支配rRNA折叠的规则。我们通过描绘其复杂的多步解链途径解构了LSU rRNA的结构域III。我们研究了结构域III以及结构域III的两个等大小的“子结构域”。综合结果与一个模型一致,即在切割成子结构域后,结构域III的解链转变是保守的。结构域III的八个解链转变中的每一个在熔解温度(Tm)和焓变(ΔH)方面都与在两个分离的子结构域之一中观察到的一个转变相对应。这些结果支持了一个模型,即结构、稳定性和折叠机制由局部相互作用主导,并且不受子结构域分离的影响。结构域III rRNA不同于那些在折叠早期形成长程协同相互作用网络或不可逆折叠的RNA。

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