Cargando…
Mechanism of TRIM25 Catalytic Activation in the Antiviral RIG-I Pathway
Antiviral response pathways induce interferon by higher-order assembly of signaling complexes called signalosomes. Assembly of the RIG-I signalosome is regulated by K63-linked polyubiquitin chains, which are synthesized by the E3 ubiquitin ligase, TRIM25. We have previously shown that the TRIM25 coi...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5076470/ https://www.ncbi.nlm.nih.gov/pubmed/27425606 http://dx.doi.org/10.1016/j.celrep.2016.06.070 |
_version_ | 1782462034396315648 |
---|---|
author | Sanchez, Jacint G. Chiang, Jessica J. Sparrer, Konstantin M.J. Alam, Steven L. Chi, Michael Roganowicz, Marcin D. Sankaran, Banumathi Gack, Michaela U. Pornillos, Owen |
author_facet | Sanchez, Jacint G. Chiang, Jessica J. Sparrer, Konstantin M.J. Alam, Steven L. Chi, Michael Roganowicz, Marcin D. Sankaran, Banumathi Gack, Michaela U. Pornillos, Owen |
author_sort | Sanchez, Jacint G. |
collection | PubMed |
description | Antiviral response pathways induce interferon by higher-order assembly of signaling complexes called signalosomes. Assembly of the RIG-I signalosome is regulated by K63-linked polyubiquitin chains, which are synthesized by the E3 ubiquitin ligase, TRIM25. We have previously shown that the TRIM25 coiled-coil domain is a stable, antiparallel dimer that positions two catalytic RING domains on opposite ends of an elongated rod. We now show that the RING domain is a separate self-association motif that engages ubiquitin-conjugated E2 enzymes as a dimer. RING dimerization is required for catalysis, TRIM25-mediated RIG-I ubiquitination, interferon induction, and antiviral activity. We also provide evidence that RING dimerization and E3 ligase activity are promoted by binding of the TRIM25 SPRY domain to the RIG-I effector domain. These results indicate that TRIM25 actively participates in higher-order assembly of the RIG-I signalosome and helps to fine-tune the efficiency of the RIG-I-mediated antiviral response. |
format | Online Article Text |
id | pubmed-5076470 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
record_format | MEDLINE/PubMed |
spelling | pubmed-50764702017-08-02 Mechanism of TRIM25 Catalytic Activation in the Antiviral RIG-I Pathway Sanchez, Jacint G. Chiang, Jessica J. Sparrer, Konstantin M.J. Alam, Steven L. Chi, Michael Roganowicz, Marcin D. Sankaran, Banumathi Gack, Michaela U. Pornillos, Owen Cell Rep Article Antiviral response pathways induce interferon by higher-order assembly of signaling complexes called signalosomes. Assembly of the RIG-I signalosome is regulated by K63-linked polyubiquitin chains, which are synthesized by the E3 ubiquitin ligase, TRIM25. We have previously shown that the TRIM25 coiled-coil domain is a stable, antiparallel dimer that positions two catalytic RING domains on opposite ends of an elongated rod. We now show that the RING domain is a separate self-association motif that engages ubiquitin-conjugated E2 enzymes as a dimer. RING dimerization is required for catalysis, TRIM25-mediated RIG-I ubiquitination, interferon induction, and antiviral activity. We also provide evidence that RING dimerization and E3 ligase activity are promoted by binding of the TRIM25 SPRY domain to the RIG-I effector domain. These results indicate that TRIM25 actively participates in higher-order assembly of the RIG-I signalosome and helps to fine-tune the efficiency of the RIG-I-mediated antiviral response. 2016-07-14 2016-08-02 /pmc/articles/PMC5076470/ /pubmed/27425606 http://dx.doi.org/10.1016/j.celrep.2016.06.070 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Sanchez, Jacint G. Chiang, Jessica J. Sparrer, Konstantin M.J. Alam, Steven L. Chi, Michael Roganowicz, Marcin D. Sankaran, Banumathi Gack, Michaela U. Pornillos, Owen Mechanism of TRIM25 Catalytic Activation in the Antiviral RIG-I Pathway |
title | Mechanism of TRIM25 Catalytic Activation in the Antiviral RIG-I Pathway |
title_full | Mechanism of TRIM25 Catalytic Activation in the Antiviral RIG-I Pathway |
title_fullStr | Mechanism of TRIM25 Catalytic Activation in the Antiviral RIG-I Pathway |
title_full_unstemmed | Mechanism of TRIM25 Catalytic Activation in the Antiviral RIG-I Pathway |
title_short | Mechanism of TRIM25 Catalytic Activation in the Antiviral RIG-I Pathway |
title_sort | mechanism of trim25 catalytic activation in the antiviral rig-i pathway |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5076470/ https://www.ncbi.nlm.nih.gov/pubmed/27425606 http://dx.doi.org/10.1016/j.celrep.2016.06.070 |
work_keys_str_mv | AT sanchezjacintg mechanismoftrim25catalyticactivationintheantiviralrigipathway AT chiangjessicaj mechanismoftrim25catalyticactivationintheantiviralrigipathway AT sparrerkonstantinmj mechanismoftrim25catalyticactivationintheantiviralrigipathway AT alamstevenl mechanismoftrim25catalyticactivationintheantiviralrigipathway AT chimichael mechanismoftrim25catalyticactivationintheantiviralrigipathway AT roganowiczmarcind mechanismoftrim25catalyticactivationintheantiviralrigipathway AT sankaranbanumathi mechanismoftrim25catalyticactivationintheantiviralrigipathway AT gackmichaelau mechanismoftrim25catalyticactivationintheantiviralrigipathway AT pornillosowen mechanismoftrim25catalyticactivationintheantiviralrigipathway |