Evidence map›Paper›PMID 25155613›Full record

ArticleMolecular cell2014

SIRT1-mediated deacetylation of CRABPII regulates cellular retinoic acid signaling and modulates embryonic stem cell differentiation.

Shuang Tang, Gang Huang, Wei Fan, Yue Chen, James M Ward, Xiaojiang Xu, Qing Xu, Ashley Kang, Michael W McBurney, David C Fargo and 4 more

Abstract read
In one paragraph

Article in Molecular cell, 2014. 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
–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

41 citing papers in PubMed.

  1. Genes · 2026
    Article
  2. Article
  3. Article
  4. Beneficial Effects ofNutrients · 2024
    Review
  5. Review
  6. Review
  7. Review
  8. The SIRT1-c-Myc axis in regulation of stem cells.Frontiers in cell and developmental biology · 2023
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. SIRT1: A Novel Protective Molecule in Pre-eclampsia.International journal of medical sciences · 2022
    Review
  14. Epigenetic Alterations under Oxidative Stress in Stem Cells.Oxidative medicine and cellular longevity · 2022
    Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review
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

14 authors.

Shuang TangDepartment of Nuclear Medicine, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200127, China; Laboratory of Signal Transduction, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.
Gang HuangDepartment of Nuclear Medicine, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200127, China. Electronic address: huang2802@163.com.
Wei FanDivision of Medical Cell Biology, Institute for Anatomy and Cell Biology II, Justus Liebig University, Aulweg 123, 35385 Giessen, Germany.
Yue ChenThe Ben May Department for Cancer Research, University of Chicago, Chicago, IL 60637, USA.
James M WardIntegrated Bioinformatics, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.
Xiaojiang XuIntegrated Bioinformatics, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.
Qing XuLaboratory of Signal Transduction, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.
Ashley KangLaboratory of Signal Transduction, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA; NIEHS Scholars Connect Program, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.
Michael W McBurneyProgram for Cancer Therapeutics, Ottawa Hospital Research Institute, Ottawa, ON, Canada K1H 8L6.
David C FargoIntegrated Bioinformatics, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.
Guang HuLaboratory of Molecular Carcinogenesis, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.
Eveline Baumgart-VogtDivision of Medical Cell Biology, Institute for Anatomy and Cell Biology II, Justus Liebig University, Aulweg 123, 35385 Giessen, Germany.
Yingming ZhaoThe Ben May Department for Cancer Research, University of Chicago, Chicago, IL 60637, USA.
Xiaoling LiLaboratory of Signal Transduction, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA. Electronic address: lix3@niehs.nih.gov.

Funding

Sirtuins and nuclear receptors in aging and age-associated diseasesZIAES102205 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI LI, XIAOLING · 2009 to 2025
$42.4M
Role of Pluripotency Factors in Pluripotent Stem Cells, Development and DiseaseZIAES102745 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI HU, GUANG · 2010 to 2025
$31.5M
Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
Proteome Characterization Center: A Genoproteomics Pipeline for Cance ResearchU24CA160036 · NCI · JOHNS HOPKINS UNIVERSITY · PI CHAN, DANIEL WANYUI, ZHANG, HUI · 2011 to 2016
$10.7M
Biochemistry of lysine crotonylation pathwayR01GM105933 · NIGMS · UNIVERSITY OF CHICAGO · PI ZHAO, YINGMING · 2013 to 2016
$1.7M
Sirtuins and nuclear receptors in aging and age-associated diseasesZ01ES102205 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI LI, XIAOLING · 2007 to 2008
$1.6M
Intramural NIH HHS ZIA ES102205NCATS NIH HHS UL1 TR000430NCI NIH HHS CA160036NCI NIH HHS U24 CA160036NIEHS NIH HHS Z01 ES102205NIGMS NIH HHS GM105933NIGMS NIH HHS R01 GM105933
6 · The paper itself

Abstract

Retinoid homeostasis is critical for normal embryonic development. Both the deficiency and excess of these compounds are associated with congenital malformations. Here we demonstrate that SIRT1, the most conserved mammalian NAD⁺-dependent protein deacetylase, contributes to homeostatic retinoic acid (RA) signaling and modulates mouse embryonic stem cell (mESC) differentiation in part through deacetylation of cellular retinoic acid binding protein II (CRABPII). We show that RA-mediated acetylation of CRABPII at K102 is essential for its nuclear accumulation and subsequent activation of RA signaling. SIRT1 interacts with and deacetylates CRABPII, regulating its subcellular localization. Consequently, SIRT1 deficiency induces hyperacetylation and nuclear accumulation of CRABPII, enhancing RA signaling and accelerating mESC differentiation in response to RA. Consistently, SIRT1 deficiency is associated with elevated RA signaling and development defects in mice. Our findings reveal a molecular mechanism that regulates RA signaling and highlight the importance of SIRT1 in regulation of ESC pluripotency and embryogenesis.

Indexed as

AcetylationAnimalsBase SequenceCell DifferentiationCell NucleusEmbryonic Stem CellsGene-Environment InteractionHEK293 CellsHumansMiceMice, Inbred C57BLMice, KnockoutMolecular Sequence DataReceptors, Retinoic AcidSignal TransductionSirtuin 1Receptors, Retinoic AcidSirtuin 1Tretinoin

Identifiers

PMID25155613
PMCPMC4228935

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.