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PXD029959

PXD029959 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleDifferential scaling between G1 protein production and cell size dynamics promotes commitment to the cell division cycle in budding yeast
DescriptionIn the unicellular eukaryote Saccharomyces cerevisiae, Cln3–cyclin-dependent kinase activity enables Start, the irreversible commitment to the cell division cycle. However, the concentration of Cln3 has been paradoxically considered to remain constant during G1, due to the presumed scaling of its production rate with cell size dynamics. Measuring metabolic and biosynthetic activity during cell cycle progression in single cells, we found that cells exhibit pulses in their protein production rate. Rather than scaling with cell size dynamics, these pulses follow the intrinsic metabolic dynamics, peaking around Start. Using a viral- based bicistronic construct and targeted proteomics to measure Cln3 at the single-cell and population levels, we show that the differential scaling between protein production and cell size leads to a temporal increase in Cln3 concentration, and passage through Start. This differential scaling causes Start in both daughter and mother cells across growth conditions. Thus, uncou- pling between two fundamental physiological parameters drives cell cycle commitment.
HostingRepositoryPRIDE
AnnounceDate2022-05-16
AnnouncementXMLSubmission_2022-05-16_05:28:00.869.xml
DigitalObjectIdentifierhttps://dx.doi.org/10.6019/PXD029959
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportSupported dataset by repository
PrimarySubmitterAlexander Schmidt
SpeciesList scientific name: Saccharomyces cerevisiae (Baker's yeast); NCBI TaxID: 4932;
ModificationListNo PTMs are included in the dataset
InstrumentOrbitrap Fusion Lumos
Dataset History
RevisionDatetimeStatusChangeLog Entry
02021-11-26 04:09:41ID requested
12022-05-16 05:25:33announced
22022-05-16 05:28:01announced2022-05-16: Updated publication reference for PubMed record(s): 35482514.
Publication List
Litsios A, Goswami P, Terpstra HM, Coffin C, Vuillemenot LA, Rovetta M, Ghazal G, Guerra P, Buczak K, Schmidt A, Tollis S, Tyers M, Royer CA, Milias-Argeitis A, Heinemann M, The timing of Start is determined primarily by increased synthesis of the Cln3 activator rather than dilution of the Whi5 inhibitor. Mol Biol Cell, 33(5):rp2(2022) [pubmed]
Keyword List
submitter keyword: Yeast, LC-MS, cell division, phosphorylation
Contact List
Alexander Schmidt
contact affiliationPCF, Biozentrum, University of Basel, Basel, Switzerland
contact emailalex.schmidt@unibas.ch
lab head
Alexander Schmidt
contact affiliationProteomics Core Facility
contact emailalex.schmidt@unibas.ch
dataset submitter
Full Dataset Link List
Dataset FTP location
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Repository Record List
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