PXD055081 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Proteomic characterization of ubiquitin carboxyl-terminal hydrolase 19 deficient cells reveals a role for USP19 in secretion of lysosomal proteins |
Description | Ubiquitin carboxyl-terminal hydrolase 19 (USP19) is a unique deubiquitinase (DUB), characterized by multiple variants generated by alternative splicing. Several variants bear a C-terminal transmembrane domain that anchors them to the endoplasmic reticulum (ER). Other than regulating protein stability by preventing proteasome degradation, USP19 has been reported to rescue substrates from ER-associated protein degradation (ERAD) in a catalytic-independent manner, promote autophagy and address proteins to lysosomal degradation via chaperone-mediated autophagy. In addition, USP19 has recently emerged as the protein responsible for the unconventional secretion of misfolded proteins including Parkinson’s disease associated protein α-synuclein. Despite mounting evidence that USP19 plays crucial roles in a number of biological processes, the underlying mechanisms are unclear due to lack of information on the physiological substrates of USP19. Herein, we used high-resolution quantitative proteomics to analyze changes in the secretome and cell proteome induced by loss of USP19, in order to identify proteins whose secretion or turnover is regulated by USP19. We found that ablation of USP19 induced significant proteomic alterations both in and out of the cell. Loss of USP19 impaired release of several lysosomal proteins, including legumain (LGMN) and several cathepsins. In order to understand the underlaying mechanism, we dissected the USP19-regulated secretion of LGMN in several cell types. We found that LGMN was not a DUB substrate of USP19 and that its USP19-dependent release did not require their direct interaction. LGMN secretion occurred by a mechanism that involved the Golgi apparatus, autophagosome formation and lysosome function. This mechanism resembled the recently described “lysosomal exocytosis”, by which LGMN and other lysosomal hydrolases are secreted, that involves ubiquitination of p62 and is regulated by other DUBs such as USP15 and USP17.
In conclusion, our proteomic characterization of USP19 has identified a collection of proteins in the secretome and within the cell that are regulated by USP19, which link USP19 to secretion of lysosomal proteins, including LGMN. |
HostingRepository | PRIDE |
AnnounceDate | 2025-05-07 |
AnnouncementXML | Submission_2025-05-07_01:10:43.581.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Simone Bonelli |
SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: 9606; |
ModificationList | acetylated residue; monohydroxylated residue; iodoacetamide derivatized residue |
Instrument | Orbitrap Exploris 480 |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2024-08-22 09:13:37 | ID requested | |
⏵ 1 | 2025-05-07 01:10:44 | announced | |
Publication List
10.1016/j.mcpro.2024.100854; |
Bonelli S, Lo Pinto M, Ye Y, M, ü, ller SA, Lichtenthaler SF, Scilabra SD, Proteomic Characterization of Ubiquitin Carboxyl-Terminal Hydrolase 19 Deficient Cells Reveals a Role for USP19 in the Secretion of Lysosomal Proteins. Mol Cell Proteomics, 23(11):100854(2024) [pubmed] |
Keyword List
submitter keyword: lysosome, cathepsins.,ubiquitin carboxyl-terminal hydrolase 19 |
proteomics |
unconventional secretion |
secretome |
legumain |
Contact List
Simone Dario |
contact affiliation | Fondazione Ri.MED |
contact email | sdscilabra@fondazionerimed.com |
lab head | |
Simone Bonelli |
contact affiliation | Ri.MED Foundation |
contact email | sbonelli@fondazionerimed.com |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD055081
- Label: PRIDE project
- Name: Proteomic characterization of ubiquitin carboxyl-terminal hydrolase 19 deficient cells reveals a role for USP19 in secretion of lysosomal proteins