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Substrate recognition by TRIM and TRIM-like proteins in innate immunity

TRIM (Tripartite motif) and TRIM-like proteins have emerged as an important class of E3 ligases in innate immunity. Their functions range from activation or regulation of innate immune signaling pathway to direct detection and restriction of pathogens. Despite the importance, molecular mechanisms fo...

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Detalles Bibliográficos
Autores principales: Wang, Hai-Tao, Hur, Sun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7572318/
https://www.ncbi.nlm.nih.gov/pubmed/33092958
http://dx.doi.org/10.1016/j.semcdb.2020.09.013
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author Wang, Hai-Tao
Hur, Sun
author_facet Wang, Hai-Tao
Hur, Sun
author_sort Wang, Hai-Tao
collection PubMed
description TRIM (Tripartite motif) and TRIM-like proteins have emerged as an important class of E3 ligases in innate immunity. Their functions range from activation or regulation of innate immune signaling pathway to direct detection and restriction of pathogens. Despite the importance, molecular mechanisms for many TRIM/TRIM-like proteins remain poorly characterized, in part due to challenges of identifying their substrates. In this review, we discuss several TRIM/TRIM-like proteins in RNA sensing pathways and viral restriction functions. We focus on those containing PRY-SPRY, the domain most frequently used for substrate recognition, and discuss emerging mechanisms that are commonly utilized by several TRIM/TRIM-like proteins to tightly control their interaction with the substrates.
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spelling pubmed-75723182020-10-20 Substrate recognition by TRIM and TRIM-like proteins in innate immunity Wang, Hai-Tao Hur, Sun Semin Cell Dev Biol Article TRIM (Tripartite motif) and TRIM-like proteins have emerged as an important class of E3 ligases in innate immunity. Their functions range from activation or regulation of innate immune signaling pathway to direct detection and restriction of pathogens. Despite the importance, molecular mechanisms for many TRIM/TRIM-like proteins remain poorly characterized, in part due to challenges of identifying their substrates. In this review, we discuss several TRIM/TRIM-like proteins in RNA sensing pathways and viral restriction functions. We focus on those containing PRY-SPRY, the domain most frequently used for substrate recognition, and discuss emerging mechanisms that are commonly utilized by several TRIM/TRIM-like proteins to tightly control their interaction with the substrates. Elsevier Ltd. 2021-03 2020-10-20 /pmc/articles/PMC7572318/ /pubmed/33092958 http://dx.doi.org/10.1016/j.semcdb.2020.09.013 Text en © 2020 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Wang, Hai-Tao
Hur, Sun
Substrate recognition by TRIM and TRIM-like proteins in innate immunity
title Substrate recognition by TRIM and TRIM-like proteins in innate immunity
title_full Substrate recognition by TRIM and TRIM-like proteins in innate immunity
title_fullStr Substrate recognition by TRIM and TRIM-like proteins in innate immunity
title_full_unstemmed Substrate recognition by TRIM and TRIM-like proteins in innate immunity
title_short Substrate recognition by TRIM and TRIM-like proteins in innate immunity
title_sort substrate recognition by trim and trim-like proteins in innate immunity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7572318/
https://www.ncbi.nlm.nih.gov/pubmed/33092958
http://dx.doi.org/10.1016/j.semcdb.2020.09.013
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