
Conditional Protein Function via N-Degron Pathway–Mediated Proteostasis in Stress Physiology
Author(s) -
Nico Dißmeyer
Publication year - 2019
Publication title -
annual review of plant biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 11.695
H-Index - 262
eISSN - 1545-2123
pISSN - 1543-5008
DOI - 10.1146/annurev-arplant-050718-095937
Subject(s) - degron , proteostasis , proteolysis , microbiology and biotechnology , biochemistry , biology , function (biology) , chemistry , amino acid , enzyme , ubiquitin , ubiquitin ligase , gene
The N-degron pathway, formerly the N-end rule pathway, regulates functions of regulatory proteins. It impacts protein half-life and therefore directs the actual presence of target proteins in the cell. The current concept holds that the N-degron pathway depends on the identity of the amino (N)-terminal amino acid and many other factors, such as the follow-up sequence at the N terminus, conformation, flexibility, and protein localization. It is evolutionarily conserved throughout the kingdoms. One possible entry point for substrates of the N-degron pathway is oxidation of N-terminal Cys residues. Oxidation of N-terminal Cys is decisive for further enzymatic modification of various neo–N termini by arginylation that generates potentially neofunctionalized or instable proteoforms. Here, I focus on the posttranslational modifications that are encompassed by protein degradation via the Cys/Arg branch of the N-degron pathway—part of the PROTEOLYSIS 6 (PRT6)/N-degron pathway—as well as the underlying physiological principles of this branch and its biological significance in stress response.