Evidence map›Paper›PMID 34114564›Full record

ArticleeLife2021

CDK control pathways integrate cell size and ploidy information to control cell division.

James Oliver Patterson, Souradeep Basu, Paul Rees, Paul Nurse

Open access · goldAbstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.1field-weighted citation impact, top 12% of its field
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

18 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
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  5. Review
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  8. Review
  9. Slower CDK4 and faster CDK2 activation in the cell cycle.Structure (London, England : 1993) · 2024
    Article
  10. The bistable mitotic switch in fission yeast.Molecular biology of the cell · 2024
    Article
  11. How do stochastic processes and genetic threshold effects explain incomplete penetrance and inform causal disease mechanisms?Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024
    Review
  12. Article
  13. Article
  14. Article
  15. A quantitative and spatial analysis of cell cycle regulators during the fission yeast cycle.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  16. Article
  17. Imaging flow cytometry: a primer.Nature reviews. Methods primers · 2022
    Article
  18. 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

4 authors at 2 institutions in 2 countries.

James Oliver PattersonCell Cycle Laboratory, The Francis Crick Institute, London, United Kingdom.ORCID 0000-0003-1993-4500
Souradeep BasuCell Cycle Laboratory, The Francis Crick Institute, London, United Kingdom.ORCID 0000-0003-4448-8688
Paul ReesCollege of Engineering, Swansea University, Swansea, United Kingdom.
Paul NurseCell Cycle Laboratory, The Francis Crick Institute, London, United Kingdom.
The Francis Crick Institute · GBBroad Institute · US

Funding

Biotechnology and Biological Sciences Research Council BB/N005163/1Biotechnology and Biological Sciences Research Council BB/P026818/1Cancer Research UK FC01121Medical Research Council FC01121Wellcome Trust 093917Wellcome Trust 214183Wellcome Trust FC001121Wellcome Trust FC01121
6 · The paper itself

Abstract

Maintenance of cell size homeostasis is a property that is conserved throughout eukaryotes. Cell size homeostasis is brought about by the co-ordination of cell division with cell growth and requires restriction of smaller cells from undergoing mitosis and cell division, whilst allowing larger cells to do so. Cyclin-CDK is the fundamental driver of mitosis and therefore ultimately ensures size homeostasis. Here we dissect determinants of CDK activity in vivo to investigate how cell size information is processed by the cell cycle network in fission yeast. We develop a high-throughput single-cell assay system of CDK activity in vivo and show that inhibitory tyrosine phosphorylation of CDK encodes cell size information, with the phosphatase PP2A aiding to set a size threshold for division. CDK inhibitory phosphorylation works synergistically with PP2A to prevent mitosis in smaller cells. Finally, we find that diploid cells of equivalent size to haploid cells exhibit lower CDK activity in response to equal cyclin-CDK enzyme concentrations, suggesting that CDK activity is reduced by increased DNA levels. Therefore, scaling of cyclin-CDK levels with cell size, CDK inhibitory phosphorylation, PP2A, and DNA-dependent inhibition of CDK activity, all inform the cell cycle network of cell size, thus contributing to cell size homeostasis.

Indexed as

Cell DivisionCell SizeCell CycleCyclin-Dependent KinasesCyclinsHomeostasisMitosisPhosphorylationPloidiesProtein Phosphatase 2SchizosaccharomycesSchizosaccharomyces pombe ProteinsCyclin-Dependent KinasesCyclinsProtein Phosphatase 2Schizosaccharomyces pombe ProteinsCDKcell biologycell cyclecell size controlcomputational biologycyclinPP2AS. pombesynthetic biologysystems biology

Identifiers

PMID34114564
PMCPMC8248981
OpenAlexW3171398397

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.