Evidence map›Paper›PMID 23468428›Full record

ArticleGenes & development2013

The tumor suppressor SirT2 regulates cell cycle progression and genome stability by modulating the mitotic deposition of H4K20 methylation.

Lourdes Serrano, Paloma Martínez-Redondo, Anna Marazuela-Duque, Berta N Vazquez, Scott J Dooley, Philipp Voigt, David B Beck, Noriko Kane-Goldsmith, Qiang Tong, Rosa M Rabanal and 5 more

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 169 papers.

0numbers the graph read from it
0cells of the map it votes in
169citing 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

169 citing papers in PubMed, 275 citations in OpenAlex.

  1. SIRT2 deacylase modulators control B cell metabolic reprogramming in EBV infection and mitogenic activation.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  3. Aging and cancer: current understandings and future perspectives.Signal transduction and targeted therapy · 2026
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  8. The Yin-Yang balance of SIRT1 and SIRT2 in cancer metabolic remodeling.International journal of biological sciences · 2026
    Review
  9. Macrophage states and polarization duringFrontiers in cellular and infection microbiology · 2026
    Review
  10. Review
  11. Regulation of Stem Cell Function by NADPhysiology (Bethesda, Md.) · 2025
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  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Reversible Acetylation of Non-histone Proteins in Human Cancers.Results and problems in cell differentiation · 2025
    Review
  18. Review
  19. Review
  20. Epigenetics-targeted drugs: current paradigms and future challenges.Signal transduction and targeted therapy · 2024
    Review

109 more citing papers are in PubMed but not listed here.

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

15 authors at 6 institutions in 3 countries.

Lourdes SerranoDepartment of Genetics, the Human Genetics Institute of New Jersey, Rutgers University, Piscataway, New Jersey 08854, USA. serrano@biology.rutgers.edu
Paloma Martínez-Redondo
Anna Marazuela-Duque
Berta N Vazquez
Scott J Dooley
Philipp Voigt
David B Beck
Noriko Kane-Goldsmith
Qiang Tong
Rosa M Rabanal
Dolors Fondevila
Purificación Muñoz
Marcus Krüger
Jay A Tischfield
Alejandro Vaquero
Rutgers, The State University of New Jersey · USInstitut d'Investigació Biomédica de Bellvitge · ESNew York University · USUniversitat Autònoma de Barcelona · ESBaylor College of Medicine · USMax Planck Institute for Heart and Lung Research · DE

Funding

TRANSCRIPTIONAL PROFILINGP30CA072720 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Chang S Chan · 1997 to 2026
$94.5M
Initiation of Transcription of Protein Coding GenesR37GM037120 · NIGMS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI REINBERG, DANNY · 2004 to 2013
$4.5M
Transcription Regulation by NC2R01GM064844 · NIGMS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI REINBERG, DANNY · 2002 to 2014
$3.3M
NCI NIH HHS P30 CA072720NIGMS NIH HHS GM064844NIGMS NIH HHS R01 GM064844NIGMS NIH HHS R37 GM037120NIGMS NIH HHS R37GM037120
6 · The paper itself

Abstract

The establishment of the epigenetic mark H4K20me1 (monomethylation of H4K20) by PR-Set7 during G2/M directly impacts S-phase progression and genome stability. However, the mechanisms involved in the regulation of this event are not well understood. Here we show that SirT2 regulates H4K20me1 deposition through the deacetylation of H4K16Ac (acetylation of H4K16) and determines the levels of H4K20me2/3 throughout the cell cycle. SirT2 binds and deacetylates PR-Set7 at K90, modulating its chromatin localization. Consistently, SirT2 depletion significantly reduces PR-Set7 chromatin levels, alters the size and number of PR-Set7 foci, and decreases the overall mitotic deposition of H4K20me1. Upon stress, the interaction between SirT2 and PR-Set7 increases along with the H4K20me1 levels, suggesting a novel mitotic checkpoint mechanism. SirT2 loss in mice induces significant defects associated with defective H4K20me1-3 levels. Accordingly, SirT2-deficient animals exhibit genomic instability and chromosomal aberrations and are prone to tumorigenesis. Our studies suggest that the dynamic cross-talk between the environment and the genome during mitosis determines the fate of the subsequent cell cycle.

Indexed as

Genomic InstabilityAcetylationAmino Acid SequenceAnimalsCell CycleCell Transformation, NeoplasticChromatinDNA DamageGene Knockout TechniquesHeLa CellsHistone-Lysine N-MethyltransferaseHistonesHumansMethylationMiceMice, KnockoutChromatinHistone-Lysine N-MethyltransferaseHistonesSIRT2 protein, humanSirt2 protein, mouseSirtuin 2

Identifiers

PMID23468428
PMCPMC3613611
OpenAlexW2133130307

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.