Evidence map›Paper›PMID 27045731›Full record

ArticleNature communications2016

Cdk1 activity acts as a quantitative platform for coordinating cell cycle progression with periodic transcription.

Gabor Banyai, Feriel Baïdi, Damien Coudreuse, Zsolt Szilagyi

Abstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. miR-196a Promotes Proliferation of Mammary Epithelial Cells by TargetingAnimals : an open access journal from MDPI · 2023
    Article
  7. Article
  8. Long-term evolution of proliferating cells using the eVOLVER platform.bioRxiv : the preprint server for biology · 2023
    Article
  9. P16Oxidative medicine and cellular longevity · 2023
    Article
  10. Review
  11. Article
  12. Article
  13. Protein Phosphatases in G1 Regulation.International journal of molecular sciences · 2020
    Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. 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.

Gabor BanyaiDepartment of Medical Biochemistry and Cell Biology, University of Gothenburg, Medicinaregatan 9A, PO Box 440, 41390 Gothenburg, Sweden.
Feriel BaïdiSyntheCell team, Institute of Genetics and Development of Rennes, CNRS UMR 6290, 2 Avenue du Pr. Léon Bernard, 35043 Rennes, France.
Damien CoudreuseSyntheCell team, Institute of Genetics and Development of Rennes, CNRS UMR 6290, 2 Avenue du Pr. Léon Bernard, 35043 Rennes, France.
Zsolt SzilagyiDepartment of Medical Biochemistry and Cell Biology, University of Gothenburg, Medicinaregatan 9A, PO Box 440, 41390 Gothenburg, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell proliferation is regulated by cyclin-dependent kinases (Cdks) and requires the periodic expression of particular gene clusters in different cell cycle phases. However, the interplay between the networks that generate these transcriptional oscillations and the core cell cycle machinery remains largely unexplored. In this work, we use a synthetic regulable Cdk1 module to demonstrate that periodic expression is governed by quantitative changes in Cdk1 activity, with different clusters directly responding to specific activity levels. We further establish that cell cycle events neither participate in nor interfere with the Cdk1-driven transcriptional program, provided that cells are exposed to the appropriate Cdk1 activities. These findings contrast with current models that propose self-sustained and Cdk1-independent transcriptional oscillations. Our work therefore supports a model in which Cdk1 activity serves as a quantitative platform for coordinating cell cycle transitions with the expression of critical genes to bring about proper cell cycle progression.

Indexed as

Gene Expression Regulation, FungalTranscription, GeneticCDC2 Protein KinaseCell CycleGene Expression ProfilingMultigene FamilyPeriodicityPurinesSchizosaccharomycesSchizosaccharomyces pombe ProteinsSignal Transduction3MB-PP1CDC2 Protein KinasePurinesSchizosaccharomyces pombe Proteins

Identifiers

PMID27045731
PMCPMC4822045

What OpenQuestion holds

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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.