Oligomerization of a Bimolecular Ribozyme Modestly Rescues its Structural Defects that Disturb Interdomain Assembly to Form the Catalytic Site.

J Mol Evol

Department of Chemistry, Graduate School of Science and Engineering, University of Toyama, Gofuku 3190, Toyama, 930-8555, Japan.

Published: August 2018

AI Article Synopsis

  • The development of cellular compartmentalization was vital in the evolution of early RNA systems, helping prevent the loss of self-replicating RNA and enabling more efficient ribozyme reactions.
  • Researchers explored how RNA components could self-assemble to create a primitive cellular-like environment that simulates cellular organization and molecular crowding.
  • They engineered a one-dimensional (1D) ribozyme assembly that partially restored function in mutated ribozymes, suggesting improved catalytic activity despite mutations.

Article Abstract

The emergence of cellular compartmentalization was a crucial step in the hypothetical RNA world and its evolution because it would not only prevent the extinction of RNA self-replication systems due to dispersion/diffusion of their components but also facilitate ribozyme reactions by molecular crowding effects. Here, we proposed and examined self-assembly of RNA components as a primitive cellular-like environment, which may have the ability to mimic cellular compartmentalization and crowding effects. We engineered a bimolecular group I ribozyme to form a one-dimensional (1D)-ribozyme assembly. In the 1D assembly form, severe mutations that inactivated the parent bimolecular ribozyme were modestly rescued resulting in weak catalytic ability.

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Source
http://dx.doi.org/10.1007/s00239-018-9862-8DOI Listing

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