Evidence map›Paper›PMID 23290551›Full record

ArticleCurrent biology : CB2013

Mechanism and regulation of Cdc25/Twine protein destruction in embryonic cell-cycle remodeling.

Jeffrey A Farrell, Patrick H O'Farrell

Abstract read
In one paragraph

Article in Current biology : CB, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing 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

43 citing papers in PubMed.

  1. Review
  2. Article
  3. Collective effects of cell cleavage dynamics.Frontiers in cell and developmental biology · 2024
    Review
  4. Review
  5. Article
  6. Temporal control of late replication and coordination of origin firing by self-stabilizing Rif1-PP1 hubs inProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  7. Article
  8. Cell cycle control during early embryogenesis.Development (Cambridge, England) · 2021
    Article
  9. Article
  10. Review
  11. The nuclear to cytoplasmic ratio directly regulates zygotic transcription inProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Mechanisms regulating zygotic genome activation.Nature reviews. Genetics · 2019
    Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Jeffrey A FarrellDepartment of Biochemistry, University of California, San Francisco, San Francisco, CA 94158, USA.
Patrick H O'Farrell

Funding

Developmental Programs of Cell Cycle ControlR37GM037193 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI O'FARRELL, PATRICK H · 2010 to 2019
$4.8M
MOLECULAR DETERMINANTS OF DEVELOPMENTAL FATER01GM037193 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI O'FARRELL, PATRICK H · 1986 to 2009
$4.4M
NIGMS NIH HHS GM037193NIGMS NIH HHS R01 GM037193NIGMS NIH HHS R37 GM037193
6 · The paper itself

Abstract

backgroundIn Drosophila embryos, the midblastula transition (MBT) dramatically remodels the cell cycle during the 14(th) interphase. Before the MBT, each cycle is composed of only a short S phase and mitosis. At the MBT, S phase is dramatically lengthened by the onset of late replication, and a G2 phase is introduced. Both changes set the stage for gastrulation and require downregulation of Cdc25 phosphatase, which was previously attributed to the elimination of its transcripts at the MBT.

resultsPremature removal of cdc25 transcripts by RNAi did not affect progression to the MBT. Instead, an antibody against the Cdc25 isoform Twine showed that Twine protein was abundant and stable until the MBT, when it was destabilized and rapidly eliminated. Persistence of pre-MBT levels of Twine was sufficient to prevent cell-cycle slowing. Twine protein destruction was timed by the nucleocytoplasmic ratio and depended on the activation of zygotic transcription at the MBT, including expression of the gene tribbles, whose activity was sufficient to trigger Twine destruction and was required for prompt Twine disappearance.

conclusionsWe propose that the developmentally regulated destruction of Twine protein is a critical switch that contributes to the cell-cycle change at the MBT, including the addition of a G2 phase and onset of late replication. Moreover, we show that this destruction is triggered by the nucleocytoplasmic ratio-dependent onset of zygotic transcription of tribbles and other unknown genes.

Indexed as

Embryonic DevelopmentS PhaseAnimalscdc25 PhosphatasesCell Cycle ProteinsCheckpoint Kinase 1Down-RegulationDrosophilaDrosophila ProteinsEmbryo, NonmammalianPhosphorylationProtein KinasesProtein Serine-Threonine KinasesProtein Tyrosine PhosphatasesTranscription, Geneticcdc25 PhosphatasesCell Cycle ProteinsCheckpoint Kinase 1Drosophila ProteinsProtein KinasesProtein Serine-Threonine KinasesProtein Tyrosine Phosphatasesstg protein, Drosophilatrbl protein, Drosophilatwe protein, Drosophila

Identifiers

PMID23290551
PMCPMC4091758

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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.