TRIM proteins and diseases

M Watanabe, S Hatakeyama - The journal of biochemistry, 2017 - academic.oup.com
M Watanabe, S Hatakeyama
The journal of biochemistry, 2017academic.oup.com
Ubiquitination is one of the posttranslational modifications that regulates a number of
intracellular events including signal transduction, protein quality control, transcription, cell
cycle, apoptosis and development. The ubiquitin system functions as a garbage machine to
degrade target proteins and as a regulator for several signalling pathways. Biochemical
reaction of ubiquitination requires several enzymes including E1, E2 and E3, and E3
ubiquitin ligases play roles as receptors for recognizing target proteins. Most of the tripartite …
Abstract
Ubiquitination is one of the posttranslational modifications that regulates a number of intracellular events including signal transduction, protein quality control, transcription, cell cycle, apoptosis and development. The ubiquitin system functions as a garbage machine to degrade target proteins and as a regulator for several signalling pathways. Biochemical reaction of ubiquitination requires several enzymes including E1, E2 and E3, and E3 ubiquitin ligases play roles as receptors for recognizing target proteins. Most of the tripartite motif (TRIM) proteins are E3 ubiquitin ligases. Recent studies have shown that some TRIM proteins function as important regulators for a variety of diseases including cancer, inflammatory diseases, infectious diseases, neuropsychiatric disorders, chromosomal abnormalities and developmental diseases. In this review, we summarize the involvement of TRIM proteins in the aetiology of various diseases.
Oxford University Press