Evidence map›Paper›PMID 31921850›Full record

ArticleFrontiers in cell and developmental biology2019

Multiple Layers of Phospho-Regulation Coordinate Metabolism and the Cell Cycle in Budding Yeast.

Lichao Zhang, Sebastian Winkler, Fabian P Schlottmann, Oliver Kohlbacher, Josh E Elias, Jan M Skotheim, Jennifer C Ewald

Abstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. When Phosphatases Go Mad: The Molecular Basis for Toxicity of Yeast Ppz1.International journal of molecular sciences · 2022
    Review
  11. Article
  12. Budding yeast relies on GScience advances · 2021
    Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Building blocks are synthesized on demand during the yeast cell cycle.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  19. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Lichao ZhangDepartment of Chemical and Systems Biology, Stanford University, Stanford, CA, United States.
Sebastian WinklerApplied Bioinformatics, Department of Computer Science, University of Tübingen, Tübingen, Germany.
Fabian P SchlottmannMolecular Cell Biology, Interfaculty Institute of Cell Biology, University of Tübingen, Tübingen, Germany.
Oliver KohlbacherApplied Bioinformatics, Department of Computer Science, University of Tübingen, Tübingen, Germany.
Josh E EliasDepartment of Chemical and Systems Biology, Stanford University, Stanford, CA, United States.
Jan M SkotheimDepartment of Biology, Stanford University, Stanford, CA, United States.
Jennifer C EwaldMolecular Cell Biology, Interfaculty Institute of Cell Biology, University of Tübingen, Tübingen, Germany.

Funding

Determining the molecular mechanism of cell size controlR01GM115479 · NIGMS · STANFORD UNIVERSITY · PI SKOTHEIM, JAN M · 2016 to 2019
$1.6M
NIGMS NIH HHS R01 GM115479
6 · The paper itself

Abstract

The coordination of metabolism and growth with cell division is crucial for proliferation. While it has long been known that cell metabolism regulates the cell division cycle, it is becoming increasingly clear that the cell division cycle also regulates metabolism. In budding yeast, we previously showed that over half of all measured metabolites change concentration through the cell cycle indicating that metabolic fluxes are extensively regulated during cell cycle progression. However, how this regulation is achieved still remains poorly understood. Since both the cell cycle and metabolism are regulated to a large extent by protein phosphorylation, we here decided to measure the phosphoproteome through the budding yeast cell cycle. Specifically, we chose a cell cycle synchronization strategy that avoids stress and nutrient-related perturbations of metabolism, and we grew the yeast on ethanol minimal medium to force cells to utilize their full biosynthetic repertoire. Using a tandem-mass-tagging approach, we found over 200 sites on metabolic enzymes and transporters to be phospho-regulated. These sites were distributed among many pathways including carbohydrate catabolism, lipid metabolism, and amino acid synthesis and therefore likely contribute to changing metabolic fluxes through the cell cycle. Among all one thousand sites whose phosphorylation increases through the cell cycle, the CDK consensus motif and an arginine-directed motif were highly enriched. This arginine-directed R-R-x-S motif is associated with protein-kinase A, which regulates metabolism and promotes growth. Finally, we also found over one thousand sites that are dephosphorylated through the G1/S transition. We speculate that the phosphatase Glc7/PP1, known to regulate both the cell cycle and carbon metabolism, may play an important role because its regulatory subunits are phospho-regulated in our data. In summary, our results identify extensive cell cycle dependent phosphorylation and dephosphorylation of metabolic enzymes and suggest multiple mechanisms through which the cell division cycle regulates metabolic signaling pathways to temporally coordinate biosynthesis with distinct phases of the cell division cycle.

Indexed as

CDKcell division cyclemetabolismphosphoproteomicsPKAPP1proliferationSaccharomyces cerevisiae

Identifiers

PMID31921850
PMCPMC6927922

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.