RNA and the Goldilocks Zone: Where Mg2+ concentration is just right

Author:

Guth-Metzler RebeccaORCID,Mohamed Ahmad Mohyeldin,Cowan Elizabeth T.ORCID,Frankel-Pinter MoranORCID,Wartell Roger M.ORCID,Glass Jennifer B.ORCID,Williams Loren DeanORCID

Abstract

AbstractMg2+, the most abundant divalent cation in cells, catalyzes RNA cleavage but can also promote RNA folding. Because folding can protect RNA from cleavage, we predicted a “Goldilocks zone”, which is a local maximum in RNA lifetime at the minimum Mg2+ concentration required for folding. By simulation and experiment, we characterized the RNA Goldilocks zone and its dependence on cleavage parameters and extent of folding. We show experimentally that yeast tRNAPhe can inhabit a Goldilocks zone. The Goldilocks phenomena appears to be robust and is tunable by changes in magnesium affinity, and a variety of other factors. Goldilocks behavior can be more pronounced for RNAs with intermediate folding states. Goldilocks behavior allows ultrafine control of RNA chemical lifetime. A subset of RNAs in vivo are expected to occupy the Goldilocks zone. In evolutionary context, Goldilocks behavior may have shaped RNA in an early Earth environment containing Mg2+ and other metals. RNAs that do not fold cannot access a Goldilocks zone.Significance StatementRNA, nature’s most fragile biopolymer, can inhabit a “Goldilocks zone” of chemical protection. Using simulation and experiment, we show that in the Goldilocks zone, RNA is protected by Mg2+ contributions to RNA folding, offsetting contributions to cleavage. RNA is shifted in and out of the Goldilocks zone by changes in [Mg2+] and by other factors. The effects of cation concentrations, temperature, RNA sequence, and chemical modification on Goldilocks behavior allow ultrafine control of RNA chemical lifetime. The RNA Goldilocks zone may have played a role in the emergence of RNA during prebiotic chemical processes.

Publisher

Cold Spring Harbor Laboratory

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3