PXD038402 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | The Respiratory Syncytial Virus M2-2 protein is targeted for proteasome degradation and inhibits translation and stress granules assembly |
Description | The M2-2 protein from the respiratory syncytial virus (RSV) is a 10 kDa protein expressed by the second ORF of the viral gene M2. During infection, M2-2 has been described as the polymerase cofactor responsible for promoting genome replication. This function was first inferred by infection with a mutant virus lacking the M2-2 ORF, in which viral genome presented delayed accumulation in comparison to wild-type virus. In accordance with this phenotype, it has been recently shown that M2-2 promotes changes in interactions between the polymerase and other viral proteins at early stages of infection. Despite its well explored role in the regulation of the polymerase activity, little has been made to investigate the relationship of M2-2 with cellular proteins. In fact, previous reports showed poor recruitment of M2-2 to viral structures, with the protein being mainly localized to the nucleus and cytoplasmic granules. To unravel which other functions M2-2 exerts during infection, we expressed the protein in HEK293T cells and performed proteomic analysis of co-immunoprecipitated partners, identifying enrichment of proteins involved with regulation of translation, protein folding and mRNA splicing. In approaches based on these data, we found that M2-2 expression downregulates eiF2α phosphorylation and inhibits stress granules assembly under arsenite induction. In addition, we also verified that M2-2 inhibits translation initiation, and is targeted for proteasome degradation, being localized to granules composed by defective ribosomal products at the cytoplasm. These results suggest that besides its functions in the regulation of genome replication, M2-2 may exert additional functions to contribute to successful RSV infection. |
HostingRepository | PRIDE |
AnnounceDate | 2023-10-24 |
AnnouncementXML | Submission_2023-10-24_11:05:12.507.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | VeronicaSantiago |
SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: 9606; |
ModificationList | acetylated residue; monohydroxylated residue; iodoacetamide derivatized residue |
Instrument | maXis |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2022-11-26 04:13:11 | ID requested | |
⏵ 1 | 2023-10-24 11:05:13 | announced | |
2 | 2023-11-14 09:07:09 | announced | 2023-11-14: Updated project metadata. |
3 | 2024-10-22 06:08:38 | announced | 2024-10-22: Updated project metadata. |
Publication List
Scudero OB, Santiago VF, Palmisano G, Simabuco FM, Ventura AM, The respiratory syncytial virus M2-2 protein is targeted for proteasome degradation and inhibits translation and stress granules assembly. PLoS One, 18(7):e0289100(2023) [pubmed] |
Keyword List
submitter keyword: RSV |
syncytial virus |
M2-2 |
translation |
stress granules |
eiF2α |
proteasome |
DRiPs |
puromycin. |
Contact List
Armando MoraisVentura |
contact affiliation | Laboratory of RNA Virus Department of Microbiology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, Brazil |
contact email | amventur@icb.usp.br |
lab head | |
VeronicaSantiago |
contact affiliation | University of Southampton |
contact email | veronicafeijoli@usp.br |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD038402
- Label: PRIDE project
- Name: The Respiratory Syncytial Virus M2-2 protein is targeted for proteasome degradation and inhibits translation and stress granules assembly