Proteomics

Dataset Information

0

SNORA33 Knockdown in chondrocytes


ABSTRACT: Background: In the experiment where we exposed chondrocytes of 4 healthy donors to OA-SF for 14 days we found several 2’O-methylation and pseudouridylation sites to be differentially modified in OA-SF condition compared to control (regular medium condition). We linked these PTMs to box C/D and H/ACA snoRNAs and selected 7 sites for validation. We did a CRISR/Cas9 mediated knock-down (KD) (not a complete knock-out (KO), as we didn’t pick clones) of these seven selected snoRNAs. Out of these seven snoRNAs, snoRNA33 knock-down stood out as the pseudouridylation at the corresposing site basically disappeared. We also saw differences in translation initiation and fidelity in snoRNA33 depleted cells. Therefore we decided to explore whether the ribosome composition (core and associated ribosomal proteins) is different in cells lacking snoRNA33 = RiboProteome samples (RP) and whether the proteome of these cells is different = Proteome samples (P). In both cases we used a GFP targeting CRISPR/Cas9 cell line as a control.

INSTRUMENT(S): Q Exactive HF

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Articular Cartilage, Articular Chondrocyte

DISEASE(S): Osteoarthritis

SUBMITTER: Mandy Peffers  

LAB HEAD: Mandy Jayne Peffers

PROVIDER: PXD042545 | Pride | 2023-10-24

REPOSITORIES: Pride

altmetric image

Publications

Depletion of <i>SNORA33</i> Abolishes ψ of 28S-U4966 and Affects the Ribosome Translational Apparatus.

Chabronova Alzbeta A   van den Akker Guus G   Housmans Bas A C BAC   Caron Marjolein M J MMJ   Cremers Andy A   Surtel Don A M DAM   Peffers Mandy J MJ   van Rhijn Lodewijk W LW   Marchand Virginie V   Motorin Yuri Y   Welting Tim J M TJM  

International journal of molecular sciences 20230808 16


Eukaryotic ribosomes are complex molecular nanomachines translating genetic information from mRNAs into proteins. There is natural heterogeneity in ribosome composition. The pseudouridylation (ψ) of ribosomal RNAs (rRNAs) is one of the key sources of ribosome heterogeneity. Nevertheless, the functional consequences of ψ-based ribosome heterogeneity and its relevance for human disease are yet to be understood. Using HydraPsiSeq and a chronic disease model of non-osteoarthritic primary human artic  ...[more]

Similar Datasets

2022-03-02 | PXD001509 | Pride
| PRJNA716861 | ENA
2023-02-21 | GSE202524 | GEO
2023-03-20 | MTBLS6402 | MetaboLights
2020-07-09 | GSE139812 | GEO
2020-07-09 | GSE140618 | GEO
2020-07-09 | GSE140622 | GEO
2011-10-24 | E-GEOD-29746 | biostudies-arrayexpress
2011-10-25 | GSE29746 | GEO
2018-08-02 | GSE117999 | GEO