Evidence map›Paper›PMID 23045395›Full record

ArticleMolecular and cellular biology2012

SIRT3 functions in the nucleus in the control of stress-related gene expression.

Toshinori Iwahara, Roberto Bonasio, Varun Narendra, Danny Reinberg

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 107 papers.

0numbers the graph read from it
0cells of the map it votes in
107citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

107 citing papers in PubMed, 194 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. NADAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Roles of SIRT3 in aging and aging-related diseases.International journal of biological sciences · 2025
    Review
  13. The Expansion of Sirtuin Gene Family in Gilthead Sea Bream (International journal of molecular sciences · 2024
    Article
  14. Sirtuins in kidney health and disease.Nature reviews. Nephrology · 2024
    Review
  15. Article
  16. Review
  17. CoClFEBS open bio · 2023
    Article
  18. Article
  19. Differential genomic effects of four nano-sized and one micro-sized CeOMaterials express : an international journal on multidisciplinary materials research · 2023
    Article
  20. Article

47 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

4 authors at 2 institutions in 1 country.

Toshinori IwaharaHoward Hughes Medical Institute, Department of Biochemistry, New York University School of Medicine, New York, New York, USA.
Roberto Bonasio
Varun Narendra
Danny Reinberg
Howard Hughes Medical Institute · USNew York University · US

Funding

Transcription Regulation by NC2R01GM064844 · NIGMS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI REINBERG, DANNY · 2002 to 2014
$3.3M
NIGMS NIH HHS GM64844-09NIGMS NIH HHS R01 GM064844
6 · The paper itself

Abstract

SIRT3 is a member of the Sir2 family of NAD(+)-dependent protein deacetylases that promotes longevity in many organisms. The processed short form of SIRT3 is a well-established mitochondrial protein whose deacetylase activity regulates various metabolic processes. However, the presence of full-length (FL) SIRT3 in the nucleus and its functional importance remain controversial. Our previous studies demonstrated that nuclear FL SIRT3 functions as a histone deacetylase and is transcriptionally repressive when artificially recruited to a reporter gene. Here, we report that nuclear FL SIRT3 is subjected to rapid degradation under conditions of cellular stress, including oxidative stress and UV irradiation, whereas the mitochondrial processed form is unaffected. FL SIRT3 degradation is mediated by the ubiquitin-proteasome pathway, at least partially through the ubiquitin protein ligase (E3) activity of SKP2. Finally, we show by chromatin immunoprecipitation that some target genes of nuclear SIRT3 are derepressed upon degradation of SIRT3 caused by stress stimuli. Thus, SIRT3 exhibits a previously unappreciated role in the nucleus, modulating the expression of some stress-related and nuclear-encoded mitochondrial genes.

Indexed as

Base SequenceCell LineCell NucleusGene Expression RegulationHEK293 CellsHeLa CellsHumansMitochondriaMutagenesis, Site-DirectedOxidative StressRecombinant ProteinsRNA, Small InterferingSequence DeletionSirtuin 3S-Phase Kinase-Associated ProteinsStress, PhysiologicalRecombinant ProteinsRNA, Small InterferingSIRT3 protein, humanSirtuin 3S-Phase Kinase-Associated ProteinsUbiquitin-Protein Ligases

Identifiers

PMID23045395
PMCPMC3510539
OpenAlexW2139884401

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.