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PXD071778

PXD071778 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleFunctional and protein interaction analysis of Nop7 in trypanosomatid parasites
DescriptionNucleolar protein 7 (Nop7), also known as PES1 or Pescadillo, is a conserved factor essential for ribosome biogenesis, cell cycle progression, proliferation, and nucleolar organization in yeast and metazoans. Its dysregulation has been linked to several non-infectious human diseases. In this study, we characterized Nop7 in the trypanosomatids parasites Trypanosoma brucei and Leishmania major, microorganisms distinguished by their atypical ribosomes whose 28S-type ribosomal RNA is multifragmented. In silico analyses indicates that trypanosomatids Nop7 contains putative structural adaptations that could be necessary for its specialized function, working as scaffold for additional protein-protein interactions. PTP-tagged version of Nop7 localize to the nucleolus throughout cell cycle in both species. To define the Nop7 interactome, we performed tandem affinity purifications followed by mass spectrometry. This proteomic approach revealed extensive association of TbNop7 and LmNop7 with numerous transient trans-acting factors, including Erb1 and Ytm1, which together with Nop7 form a heterotrimeric subcomplex (known as the PeBow complex in mammals) required for the 60S ribosome subunit maturation in other eukaryotes. We also identified several hypothetical nucleolar proteins, representing potential novel components of the trypanosomatid ribosome biogenesis machinery. Comparative proteomic features between trypanosomatids and human underscoring parasite-specific factors potentially needed for ribosome production pathways. RNAi-mediated depletion of Nop7 in T. brucei significantly impaired proliferation, induced pronounced morphological abnormalities, and altered DNA content, highlighting its critical role in cell cycle progression and survival. Collectively, our findings provide the first proteomic characterization of Nop7-associated factors in T. brucei and L. major in culture, revealing new candidates for functional investigation and potential therapeutic targeting.
HostingRepositoryPRIDE
AnnounceDate2026-05-14
AnnouncementXMLSubmission_2026-05-14_08:58:09.024.xml
DigitalObjectIdentifierhttps://doi.org/10.6019/PXD071778
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportSupported dataset by repository
PrimarySubmitterEbbing de Jong
SpeciesList scientific name: Leishmania major strain Friedlin; NCBI TaxID: NEWT:347515; scientific name: Trypanosoma brucei; NCBI TaxID: NEWT:5691;
ModificationListNo PTMs are included in the dataset
InstrumentOrbitrap Fusion Lumos
Dataset History
RevisionDatetimeStatusChangeLog Entry
02025-12-09 13:21:37ID requested
12026-05-14 08:58:09announced
Publication List
10.6019/PXD071778;
10.1016/J.JPROT.2026.105675;
Keyword List
submitter keyword: Trypanosoma brucei, proteomics, Leishmania major, nucleolus, ribosome biogenesis,Nop7
Contact List
Tomás Nepomuceno Mejía
contact affiliationUnidad de Biomedicina, Facultad de Estudios Superiores Iztacala, Universidad Nacional Autónoma de México. Av. de los Barrios 1, Col. Los Reyes Iztacala, CP 54090, Tlalnepantla de Baz, Edo. de México, México
contact emailtnepomuceno@unam.mx
lab head
Ebbing de Jong
contact affiliationSUNY Upstate Medical University
contact emaildejonge@upstate.edu
dataset submitter
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