Transformation of autophagic SQSTM1 droplets to SQSTM1-dependent P-bodies
dc.contributor.author | Valionyte, E | |
dc.contributor.author | Barrow, ER | |
dc.contributor.author | Baxter, CR | |
dc.contributor.author | Herath, S | |
dc.contributor.author | Luo, S | |
dc.date.accessioned | 2024-05-01T10:25:53Z | |
dc.date.available | 2024-05-01T10:25:53Z | |
dc.date.issued | 2024 | |
dc.identifier.issn | 1554-8627 | |
dc.identifier.issn | 1554-8635 | |
dc.identifier.uri | https://pearl.plymouth.ac.uk/handle/10026.1/22372 | |
dc.description.abstract |
SQSTM1/p62 droplets play crucial roles in droplets-based macroautophagy/autophagy including selective autophagy and bulk autophagy. We observed that under several stress milieus, SQSTM1 droplets entirely colocalize with P-body markers, and these stress-induced SQSTM1 droplets contain mRNAs. We thus determined that under certain stress conditions, autophagic SQSTM1 droplets are converted to a type of enlarged P-bodies, designated SQSTM1/p62-dependent P-bodies (pd-PBs). Stress-enhanced SQSTM1 droplet formation drives the nucleation of pd-PBs through the interaction between SQSTM1 and the RNA-binding protein DDX6. Furthermore, pd-PBs sequester PYCARD, facilitating the assembly of NLRP3 inflammasomes, and in turn induce inflammation-related cytotoxicity. Our study suggests that under stress settings, autophagic SQSTM1 droplets are transformed to pd-PBs, underlining a critical role of SQSTM1 in P-body condensation. | |
dc.format.extent | 1-2 | |
dc.format.medium | Print-Electronic | |
dc.language | en | |
dc.publisher | Informa UK Limited | |
dc.subject | Autophagy | |
dc.subject | NLRP3 inflammasome | |
dc.subject | P-bodies | |
dc.subject | PYCARD | |
dc.subject | SQSTM1 | |
dc.title | Transformation of autophagic SQSTM1 droplets to SQSTM1-dependent P-bodies | |
dc.type | journal-article | |
dc.type | Article | |
dc.type | Early Access | |
plymouth.author-url | https://www.ncbi.nlm.nih.gov/pubmed/38600662 | |
plymouth.issue | ahead-of-print | |
plymouth.volume | ahead-of-print | |
plymouth.publisher-url | http://dx.doi.org/10.1080/15548627.2024.2340413 | |
plymouth.publication-status | Published online | |
plymouth.journal | Autophagy | |
dc.identifier.doi | 10.1080/15548627.2024.2340413 | |
plymouth.organisational-group | |Plymouth | |
plymouth.organisational-group | |Plymouth|Research Groups | |
plymouth.organisational-group | |Plymouth|Faculty of Health | |
plymouth.organisational-group | |Plymouth|Research Groups|Institute of Translational and Stratified Medicine (ITSMED) | |
plymouth.organisational-group | |Plymouth|Research Groups|Institute of Translational and Stratified Medicine (ITSMED)|CBR | |
plymouth.organisational-group | |Plymouth|REF 2021 Researchers by UoA | |
plymouth.organisational-group | |Plymouth|Users by role | |
plymouth.organisational-group | |Plymouth|Users by role|Current Academic staff | |
plymouth.organisational-group | |Plymouth|REF 2021 Researchers by UoA|UoA01 Clinical Medicine | |
plymouth.organisational-group | |Plymouth|Faculty of Health|Peninsula Medical School | |
plymouth.organisational-group | |Plymouth|Users by role|Researchers in ResearchFish submission | |
plymouth.organisational-group | |Plymouth|REF 2029 Researchers by UoA | |
plymouth.organisational-group | |Plymouth|REF 2029 Researchers by UoA|UoA01 Clinical Medicine | |
dc.publisher.place | United States | |
dcterms.dateAccepted | 2024-04-04 | |
dc.date.updated | 2024-05-01T10:25:52Z | |
dc.rights.embargodate | 2024-5-3 | |
dc.identifier.eissn | 1554-8635 | |
dc.rights.embargoperiod | ||
rioxxterms.versionofrecord | 10.1080/15548627.2024.2340413 |