Evidence map›Paper›PMID 36092730›Full record

ArticleFrontiers in cell and developmental biology2022

The cell cycle inhibitor RB is diluted in G1 and contributes to controlling cell size in the mouse liver.

Shuyuan Zhang, Evgeny Zatulovskiy, Julia Arand, Julien Sage, Jan M Skotheim

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Cell size modulates ferroptosis susceptibility.bioRxiv : the preprint server for biology · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. A Fkh1/2 binding site array in thebioRxiv : the preprint server for biology · 2025
    Article
  9. Article
  10. The GScience advances · 2024
    Article
  11. Review
  12. The G1/S transition is promoted by Rb degradation via the E3 ligase UBR5.bioRxiv : the preprint server for biology · 2024
    Article
  13. 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

5 authors at 2 institutions in 1 country.

Shuyuan ZhangDepartment of Biology, Stanford University, Stanford, CA, United States.
Evgeny ZatulovskiyDepartment of Biology, Stanford University, Stanford, CA, United States.
Julia ArandDepartments of Pediatrics and Genetics, School of Medicine, Stanford University, Stanford, CA, United States.
Julien SageDepartments of Pediatrics and Genetics, School of Medicine, Stanford University, Stanford, CA, United States.
Jan M SkotheimDepartment of Biology, Stanford University, Stanford, CA, United States.
Stanford University · USChan Zuckerberg Initiative (United States) · 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 mechanisms linking cell growth to the cell cycle in the liverR01DK128578 · NIDDK · STANFORD UNIVERSITY · PI SKOTHEIM, JAN M · 2021 to 2024
$1.4M
Determine how protein synthesis is regulated during cell growth and divisionK99GM147351 · NIGMS · STANFORD UNIVERSITY · PI ZHANG, SHUYUAN · 2022 to 2023
$225k
NCI NIH HHS P01 CA254867NIDDK NIH HHS R01 DK128578NIGMS NIH HHS K99 GM147351NIGMS NIH HHS R35 GM134858
6 · The paper itself

Abstract

Every type of cell in an animal maintains a specific size, which likely contributes to its ability to perform its physiological functions. While some cell size control mechanisms are beginning to be elucidated through studies of cultured cells, it is unclear if and how such mechanisms control cell size in an animal. For example, it was recently shown that RB, the retinoblastoma protein, was diluted by cell growth in G1 to promote size-dependence of the G1/S transition. However, it remains unclear to what extent the RB-dilution mechanism controls cell size in an animal. We therefore examined the contribution of RB-dilution to cell size control in the mouse liver. Consistent with the RB-dilution model, genetic perturbations decreasing RB protein concentrations through inducible shRNA expression or through liver-specific

Indexed as

cell sizeG1/Sinhibitor dilutionmouse liverretinablastoma protein

Identifiers

PMID36092730
PMCPMC9452963
OpenAlexW4293016744

What OpenQuestion holds

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LicenceCC BY
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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.