Evidence map›Paper›PMID 15572683›Full record

ArticleMolecular and cellular biology2004

Growth rate and cell size modulate the synthesis of, and requirement for, G1-phase cyclins at start.

Brandt L Schneider, Jian Zhang, J Markwardt, George Tokiwa, Tom Volpe, Sangeet Honey, Bruce Futcher

Abstract readComparative Study
In one paragraph

Article in Molecular and cellular biology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

41 citing papers in PubMed, 72 citations in OpenAlex.

  1. Article
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  6. Review
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  9. Review
  10. Article
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  12. Article
  13. Temporal precision of regulated gene expression.PLoS computational biology · 2018
    Article
  14. Growth Rate as a Direct Regulator of the Start Network to Set Cell Size.Frontiers in cell and developmental biology · 2017
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Start and the restriction point.Current opinion in cell biology · 2013
    Review
  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

7 authors at 4 institutions in 1 country.

Brandt L SchneiderDepartment of Cell Biology and Biochemistry, Texas Tech University Health Sciences Center, 3601 4th St., Lubbock, TX 79430, USA. brandt.schneider@ttuhsc.edu
Jian Zhang
J Markwardt
George Tokiwa
Tom Volpe
Sangeet Honey
Bruce Futcher
Cold Spring Harbor Laboratory · USState University of New York · USTexas Tech University · USTexas Tech University Health Sciences Center · US

Funding

SIZE CONTROL &COMMITMENT TO DIVISION IN S. CEREVISIAER01GM039978 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI FUTCHER, BRUCE BRUCE · 1988 to 2014
$4.3M
NIGMS NIH HHS GM 39978NIGMS NIH HHS R01 GM039978
6 · The paper itself

Abstract

In Saccharomyces cerevisiae, commitment to cell cycle progression occurs at Start. Progression past Start requires cell growth and protein synthesis, a minimum cell size, and G(1)-phase cyclins. We examined the relationships among these factors. Rapidly growing cells expressed, and required, dramatically more Cln protein than did slowly growing cells. To clarify the role of cell size, we expressed defined amounts of CLN mRNA in cells of different sizes. When Cln was expressed at nearly physiological levels, a critical threshold of Cln expression was required for cell cycle progression, and this critical threshold varied with both cell size and growth rate: as cells grew larger, they needed less CLN mRNA, but as cells grew faster, they needed more Cln protein. At least in part, large cells had a reduced requirement for CLN mRNA because large cells generated more Cln protein per unit of mRNA than did small cells. When Cln was overexpressed, it was capable of promoting Start rapidly, regardless of cell size or growth rate. In summary, the amount of Cln required for Start depends dramatically on both cell size and growth rate. Large cells generate more Cln1 or Cln2 protein for a given amount of CLN mRNA, suggesting the existence of a novel posttranscriptional size control mechanism.

Indexed as

Cell CycleCell SizeG1 PhaseBlotting, WesternCyclinsGene Expression Regulation, FungalGenes, FungalHalf-LifeKineticsModels, BiologicalPrecipitin TestsPromoter Regions, GeneticProtein Processing, Post-TranslationalRNA, MessengerSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsCLN1 protein, S cerevisiaeCLN2 protein, S cerevisiaeCyclinsRNA, MessengerSaccharomyces cerevisiae Proteins

Identifiers

PMID15572683
PMCPMC533974
OpenAlexW2006545082

What OpenQuestion holds

Textmetadata
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.