Evidence map›Paper›PMID 38722822›Full record

ArticleThe Journal of cell biology2024

Cell growth and nutrient availability control the mitotic exit signaling network in budding yeast.

Rafael A Talavera, Beth E Prichard, Robert A Sommer, Ricardo M Leitao, Christopher J Sarabia, Semin Hazir, Joao A Paulo, Steven P Gygi, Douglas R Kellogg

Abstract read
In one paragraph

Article in The Journal of cell biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. 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

9 authors.

Rafael A TalaveraDepartment of Molecular, Cell and Developmental Biology, University of California, Santa Cruz, CA, USA.ORCID 0000-0002-1610-9153
Beth E PrichardDepartment of Molecular, Cell and Developmental Biology, University of California, Santa Cruz, CA, USA.ORCID 0009-0007-9372-6175
Robert A SommerDepartment of Molecular, Cell and Developmental Biology, University of California, Santa Cruz, CA, USA.ORCID 0000-0003-4529-0542
Ricardo M LeitaoDepartment of Molecular, Cell and Developmental Biology, University of California, Santa Cruz, CA, USA.ORCID 0000-0002-0916-7945
Christopher J SarabiaDepartment of Molecular, Cell and Developmental Biology, University of California, Santa Cruz, CA, USA.ORCID 0000-0003-3029-433X
Semin HazirDepartment of Molecular, Cell and Developmental Biology, University of California, Santa Cruz, CA, USA.ORCID 0009-0009-5304-3139
Joao A PauloDepartment of Cell Biology, Harvard Medical School, Boston, MA, USA.ORCID 0000-0002-4291-413X
Steven P GygiDepartment of Cell Biology, Harvard Medical School, Boston, MA, USA.ORCID 0000-0001-7626-0034
Douglas R KelloggDepartment of Molecular, Cell and Developmental Biology, University of California, Santa Cruz, CA, USA.ORCID 0000-0002-5050-2194

Funding

Control of Cell Growth and SizeR35GM131826 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI Douglas R. Kellogg · 2019 to 2026
$3.9M
NIGMS NIH HHS R35 GM131826NIH HHS R35 GM131826
6 · The paper itself

Abstract

Cell growth is required for cell cycle progression. The amount of growth required for cell cycle progression is reduced in poor nutrients, which leads to a reduction in cell size. In budding yeast, nutrients can influence cell size by modulating the extent of bud growth, which occurs predominantly in mitosis. However, the mechanisms are unknown. Here, we used mass spectrometry to identify proteins that modulate bud growth in response to nutrient availability. This led to the discovery that nutrients regulate numerous components of the mitotic exit network (MEN), which controls exit from mitosis. A key component of the MEN undergoes gradual multisite phosphorylation during bud growth that is dependent upon bud growth and correlated with the extent of growth. Furthermore, activation of the MEN is sufficient to override a growth requirement for mitotic exit. The data suggest a model in which the MEN ensures that mitotic exit occurs only when an appropriate amount of bud growth has occurred.

Indexed as

MitosisSaccharomyces cerevisiaeSignal TransductionCell Cycle ProteinsNutrientsPhosphorylationSaccharomyces cerevisiae ProteinsSaccharomycetalesCell Cycle ProteinsNutrientsSaccharomyces cerevisiae Proteins

Identifiers

PMID38722822
PMCPMC11082370

What OpenQuestion holds

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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.