Abstract
The majority of tRNA studies has focused on tRNA molecules as pivotal player in the fundamental process of protein synthesis. Mounting studies have unveiled further functions for tRNA beyond protein synthesis, including non-ribosomal amino acid transfer, and regulation of targeted proteolysis. Post-translational N-terminal arginylation of protein fragments, a non-ribosomal amino acid transfer, is one of the crucial ways by which tRNA participates in various protein degradation trajectories and influences global cellular functions. Previous studies demonstrated a role of arginylation by arginyltransferases (ATEs) in protein degradation, autophagy, and cell death in mammalian cells. Notably, recent investigations in plants have revealed some of the crucial aspects regarding the biochemical nature of Nterminal arginylation and some of its physiological roles. Herein, we review some of the key data on Nterminal arginylation of protein fragments with respect to targeted proteolysis in mammalian cells. Future mechanistic studies using state of the art approaches and physiologically-relevant cellular models are warranted to enhance our molecular understanding of this important yet enigmatic protein modification.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.