Evidence map›Paper›PMID 32109398›Full record

ArticleCurrent biology : CB2020

A G1 Sizer Coordinates Growth and Division in the Mouse Epidermis.

Shicong Xie, Jan M Skotheim

Open access · bronzeAbstract read
In one paragraph

Article in Current biology : CB, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

48 citing papers in PubMed, 94 citations in OpenAlex.

  1. Article
  2. Physical traits of supercompetitors in cell competition.Journal of the Royal Society, Interface · 2025
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  9. The GScience advances · 2024
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  10. Review
  11. A GeneralizedbioRxiv : the preprint server for biology · 2024
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  12. Proliferation symmetry breaking in growing tissues.bioRxiv : the preprint server for biology · 2024
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  13. Article
  14. Article
  15. The G1/S transition is promoted by Rb degradation via the E3 ligase UBR5.bioRxiv : the preprint server for biology · 2024
    Article
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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

2 authors at 1 institution in 1 country.

Shicong XieDepartment of Biology, Stanford University, Stanford, CA 94305, USA.
Jan M SkotheimDepartment of Biology, Stanford University, Stanford, CA 94305, USA. Electronic address: skotheim@stanford.edu.
Stanford University · US

Funding

Project 3: Defining and targeting mechanisms of E2F transcription factor regulationP01CA254867 · NCI · STANFORD UNIVERSITY · PI PETER Kent JACKSON · 2022 to 2026
$8.9M
Determining how cell growth triggers cell divisionR35GM134858 · NIGMS · STANFORD UNIVERSITY · PI Jan M Skotheim · 2020 to 2026
$4.1M
Determining the molecular mechanism of cell size controlR01GM115479 · NIGMS · STANFORD UNIVERSITY · PI SKOTHEIM, JAN M · 2016 to 2019
$1.6M
Determining how the G1/S cell cycle transition regulates the homeostasis of adult intestinal stem cellsF32GM129878 · NIGMS · STANFORD UNIVERSITY · PI XIE, SHICONG · 2018 to 2020
$113k
NCI NIH HHS P01 CA254867NIGMS NIH HHS F32 GM129878NIGMS NIH HHS R01 GM115479NIGMS NIH HHS R35 GM134858
6 · The paper itself

Abstract

Cell size homeostasis is often achieved by coupling cell-cycle progression to cell growth. Growth has been shown to drive cell-cycle progression in bacteria and yeast through "sizers," wherein cells of varying birth size divide at similar final sizes [1-3], and "adders," wherein cells increase in size a fixed amount per cell cycle [4-6]. Intermediate control phenomena are also observed, and even the same organism can exhibit different control phenomena depending on growth conditions [2, 7, 8]. Although studying unicellular organisms in laboratory conditions may give insight into their growth control in the wild, this is less apparent for studies of mammalian cells growing outside the organism. Sizers, adders, and intermediate phenomena have been observed in vitro [9-12], but it is unclear how this relates to mammalian cell proliferation in vivo. To address this question, we analyzed time-lapse images of the mouse epidermis taken over 1 week during normal tissue turnover [13]. We quantified the 3D volume growth and cell-cycle progression of single cells within the mouse skin. In dividing epidermal stem cells, we found that cell growth is coupled to division through a sizer operating largely in the G1 phase of the cell cycle. Thus, although the majority of tissue culture studies have identified adders, our analysis demonstrates that sizers are important in vivo and highlights the need to determine their underlying molecular origin.

Indexed as

Cell DivisionG1 PhaseAnimalsCell SizeEpidermal CellsMicecell cyclecell growthcell size controlG1/S controlrestriction pointsizersystems biology

Identifiers

PMID32109398
PMCPMC7158888
OpenAlexW3006926844

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.