The Role of 3′ to 5′ Reverse RNA Polymerization in tRNA Fidelity and Repair

The tRNA<sup>His</sup> guanylyltransferase (Thg1) superfamily includes enzymes that are found in all three domains of life that all share the common ability to catalyze the 3&#8242; to 5&#8242; synthesis of nucleic acids. This catalytic activity, which is the reverse of all other...

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Bibliographic Details
Main Authors: Allan W. Chen, Malithi I. Jayasinghe, Christina Z. Chung, Bhalchandra S. Rao, Rosan Kenana, Ilka U. Heinemann, Jane E. Jackman
Format: Article
Language:English
Published: MDPI AG 2019-03-01
Series:Genes
Subjects:
Online Access:https://www.mdpi.com/2073-4425/10/3/250
Description
Summary:The tRNA<sup>His</sup> guanylyltransferase (Thg1) superfamily includes enzymes that are found in all three domains of life that all share the common ability to catalyze the 3&#8242; to 5&#8242; synthesis of nucleic acids. This catalytic activity, which is the reverse of all other known DNA and RNA polymerases, makes this enzyme family a subject of biological and mechanistic interest. Previous biochemical, structural, and genetic investigations of multiple members of this family have revealed that Thg1 enzymes use the 3&#8242; to 5&#8242; chemistry for multiple reactions in biology. Here, we describe the current state of knowledge regarding the catalytic features and biological functions that have been so far associated with Thg1 and its homologs. Progress toward the exciting possibility of utilizing this unusual protein activity for applications in biotechnology is also discussed.
ISSN:2073-4425