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PXD024993

PXD024993 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleStructured elements drive circular RNA translation and expand the human proteome, part1
DescriptionThe human genome encodes tens of thousands circular RNAs (circRNAs) whose levels correlate with many disease states. While studies have focused on the non-coding functions of circRNAs, emerging evidence suggests that a handful of circRNAs encode proteins. Translation canonically starts by recognition of mRNA 5’cap and scanning to the start codon; how circRNA translation initiates remains unclear. Here, we developed a high-throughput screen to systematically identify and quantify RNA sequences that can direct circRNA translation. We identify and validate over 17,000 circRNA internal ribosome entry sites (IRES) and reveal that 18S rRNA complementarity and a structured RNA element on the IRES are important for facilitating circRNA cap-independent translation. With genomic and peptidomic analyses of the IRES, we identified nearly 1,000 putative endogenous protein-coding circRNAs and hundreds of translational units encoded by these circRNAs. We further characterized circFGFR1p, a protein encoded by circFGFR1, functions as a negative regulator of FGFR1 to suppress cell growth under stress conditions. The circRNA proteome may be important links among circRNA, biological control, and disease.
HostingRepositoryPRIDE
AnnounceDate2021-08-23
AnnouncementXMLSubmission_2021-08-22_23:53:00.163.xml
DigitalObjectIdentifierhttps://dx.doi.org/10.6019/PXD024993
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportSupported dataset by repository
PrimarySubmitterChun-Kan Chen
SpeciesList scientific name: Homo sapiens (Human); NCBI TaxID: 9606;
ModificationListmonohydroxylated residue; acetylated residue; iodoacetamide derivatized residue
InstrumentQ Exactive
Dataset History
RevisionDatetimeStatusChangeLog Entry
02021-03-25 03:23:25ID requested
12021-08-22 23:53:00announced
Publication List
Dataset with its publication pending
Keyword List
submitter keyword: LC-MS/MS
Contact List
Howard Y. Chang
contact affiliationStanford School of Medicine
contact emailhowchang@stanford.edu
lab head
Chun-Kan Chen
contact affiliationStanford University
contact emailchunkanc@stanford.edu
dataset submitter
Full Dataset Link List
Dataset FTP location
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PRIDE project URI
Repository Record List
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