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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2021
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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. |
format | Online Article Text |
id | pubmed-7572318 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT wanghaitao substraterecognitionbytrimandtrimlikeproteinsininnateimmunity AT hursun substraterecognitionbytrimandtrimlikeproteinsininnateimmunity |