High resolution profiling of cell cycle-dependent protein and phosphorylation abundance changes in non-transformed cells

Abstract The cell cycle governs a precise series of molecular events, regulated by coordinated changes in protein and phosphorylation abundance, that culminates in the generation of two daughter cells. Here, we present a proteomic and phosphoproteomic analysis of the human cell cycle in hTERT-RPE-1...

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Main Authors: Camilla Rega, Ifigenia Tsitsa, Theodoros I. Roumeliotis, Izabella Krystkowiak, Maria Portillo, Lu Yu, Julia Vorhauser, Jonathon Pines, Jörg Mansfeld, Jyoti Choudhary, Norman E. Davey
Format: Article
Language:English
Published: Nature Portfolio 2025-03-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-025-57537-8
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author Camilla Rega
Ifigenia Tsitsa
Theodoros I. Roumeliotis
Izabella Krystkowiak
Maria Portillo
Lu Yu
Julia Vorhauser
Jonathon Pines
Jörg Mansfeld
Jyoti Choudhary
Norman E. Davey
author_facet Camilla Rega
Ifigenia Tsitsa
Theodoros I. Roumeliotis
Izabella Krystkowiak
Maria Portillo
Lu Yu
Julia Vorhauser
Jonathon Pines
Jörg Mansfeld
Jyoti Choudhary
Norman E. Davey
author_sort Camilla Rega
collection DOAJ
description Abstract The cell cycle governs a precise series of molecular events, regulated by coordinated changes in protein and phosphorylation abundance, that culminates in the generation of two daughter cells. Here, we present a proteomic and phosphoproteomic analysis of the human cell cycle in hTERT-RPE-1 cells using deep quantitative mass spectrometry by isobaric labelling. By analysing non-transformed cells and improving the temporal resolution and coverage of key cell cycle regulators, we present a dataset of cell cycle-dependent protein and phosphorylation site oscillation that offers a foundational reference for investigating cell cycle regulation. These data reveal regulatory intricacies including proteins and phosphorylation sites exhibiting cell cycle-dependent oscillation, and proteins targeted for degradation during mitotic exit. Integrated with complementary resources, our data link cycle-dependent abundance dynamics to functional changes and are accessible through the Cell Cycle database (CCdb), an interactive web-based resource for the cell cycle community.
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institution DOAJ
issn 2041-1723
language English
publishDate 2025-03-01
publisher Nature Portfolio
record_format Article
series Nature Communications
spelling doaj-art-e9cb99e71d0944f6870e32d6de20266a2025-08-20T03:01:41ZengNature PortfolioNature Communications2041-17232025-03-0116111810.1038/s41467-025-57537-8High resolution profiling of cell cycle-dependent protein and phosphorylation abundance changes in non-transformed cellsCamilla Rega0Ifigenia Tsitsa1Theodoros I. Roumeliotis2Izabella Krystkowiak3Maria Portillo4Lu Yu5Julia Vorhauser6Jonathon Pines7Jörg Mansfeld8Jyoti Choudhary9Norman E. Davey10Division of Cancer Biology, The Institute of Cancer ResearchDivision of Cancer Biology, The Institute of Cancer ResearchDivision of Cancer Biology, The Institute of Cancer ResearchDivision of Cancer Biology, The Institute of Cancer ResearchDivision of Cancer Biology, The Institute of Cancer ResearchDivision of Cancer Biology, The Institute of Cancer ResearchDivision of Cancer Biology, The Institute of Cancer ResearchDivision of Cancer Biology, The Institute of Cancer ResearchDivision of Cancer Biology, The Institute of Cancer ResearchDivision of Cancer Biology, The Institute of Cancer ResearchDivision of Cancer Biology, The Institute of Cancer ResearchAbstract The cell cycle governs a precise series of molecular events, regulated by coordinated changes in protein and phosphorylation abundance, that culminates in the generation of two daughter cells. Here, we present a proteomic and phosphoproteomic analysis of the human cell cycle in hTERT-RPE-1 cells using deep quantitative mass spectrometry by isobaric labelling. By analysing non-transformed cells and improving the temporal resolution and coverage of key cell cycle regulators, we present a dataset of cell cycle-dependent protein and phosphorylation site oscillation that offers a foundational reference for investigating cell cycle regulation. These data reveal regulatory intricacies including proteins and phosphorylation sites exhibiting cell cycle-dependent oscillation, and proteins targeted for degradation during mitotic exit. Integrated with complementary resources, our data link cycle-dependent abundance dynamics to functional changes and are accessible through the Cell Cycle database (CCdb), an interactive web-based resource for the cell cycle community.https://doi.org/10.1038/s41467-025-57537-8
spellingShingle Camilla Rega
Ifigenia Tsitsa
Theodoros I. Roumeliotis
Izabella Krystkowiak
Maria Portillo
Lu Yu
Julia Vorhauser
Jonathon Pines
Jörg Mansfeld
Jyoti Choudhary
Norman E. Davey
High resolution profiling of cell cycle-dependent protein and phosphorylation abundance changes in non-transformed cells
Nature Communications
title High resolution profiling of cell cycle-dependent protein and phosphorylation abundance changes in non-transformed cells
title_full High resolution profiling of cell cycle-dependent protein and phosphorylation abundance changes in non-transformed cells
title_fullStr High resolution profiling of cell cycle-dependent protein and phosphorylation abundance changes in non-transformed cells
title_full_unstemmed High resolution profiling of cell cycle-dependent protein and phosphorylation abundance changes in non-transformed cells
title_short High resolution profiling of cell cycle-dependent protein and phosphorylation abundance changes in non-transformed cells
title_sort high resolution profiling of cell cycle dependent protein and phosphorylation abundance changes in non transformed cells
url https://doi.org/10.1038/s41467-025-57537-8
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