Evidence map›Paper›PMID 19174463›Full record

ArticleJournal of cell science2009

Involvement of SIRT7 in resumption of rDNA transcription at the exit from mitosis.

Alice Grob, Pascal Roussel, Jane E Wright, Brian McStay, Danièle Hernandez-Verdun, Valentina Sirri

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cell science, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 86 papers.

0numbers the graph read from it
0cells of the map it votes in
86citing papers in PubMed
5.2field-weighted citation impact, top 5% 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

86 citing papers in PubMed, 152 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Review
  5. Causality of Aging Hallmarks.Aging and disease · 2025
    Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. The dark side of SIRT7.Molecular and cellular biochemistry · 2024
    Review
  11. A Molecular Perspective and Role of NADInternational journal of molecular sciences · 2024
    Review
  12. The role of SIRT3 in homeostasis and cellular health.Frontiers in cellular neuroscience · 2024
    Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. SIRT7 in the aging process.Cellular and molecular life sciences : CMLS · 2022
    Review
  19. Sirtuins play critical and diverse roles in acute kidney injury.Pediatric nephrology (Berlin, Germany) · 2021
    Review
  20. Genes · 2021
    Review

26 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

6 authors at 5 institutions in 2 countries.

Alice GrobInstitut Jacques Monod, UMR 7592 CNRS/Universités Paris 6 et 7, 2 Place Jussieu, 75251 Paris Cedex 05, France.
Pascal Roussel
Jane E Wright
Brian McStay
Danièle Hernandez-Verdun
Valentina Sirri
Ninewells Hospital · GBCentre National de la Recherche Scientifique · FRInstitut Jacques Monod · FRSorbonne Université · FRUnit of Functional and Adaptive Biology · FR

Funding

Medical Research Council G0500323
6 · The paper itself

Abstract

Sirtuins, also designated class III histone deacetylases, are implicated in the regulation of cell division, apoptosis, DNA damage repair, genomic silencing and longevity. The nucleolar Sirtuin7 (SIRT7) was reported to be involved in the regulation of ribosomal gene (rDNA) transcription, but there are no data concerning the regulation of SIRT7 during the cell cycle. Here we have analyzed the behavior of endogenous SIRT7 during mitosis, while rDNA transcription is repressed. SIRT7 remains associated with nucleolar organizer regions, as does the RNA polymerase I machinery. SIRT7 directly interacts with the rDNA transcription factor UBF. Moreover, SIRT7 is phosphorylated via the CDK1-cyclin B pathway during mitosis and dephosphorylated by a phosphatase sensitive to okadaic acid at the exit from mitosis before onset of rDNA transcription. Interestingly, dephosphorylation events induce a conformational modification of the carboxy-terminal region of SIRT7 before the release of mitotic repression of rDNA transcription. As SIRT7 activity is required to resume rDNA transcription in telophase, we propose that this conformational modification regulates onset of rDNA transcription.

Indexed as

DNA, RibosomalMitosisProtein Processing, Post-TranslationalTranscriptional ActivationCDC2 Protein KinaseCell CycleCyclin BHeLa CellsHumansMetabolic Networks and PathwaysNucleolus Organizer RegionPhosphoric Monoester HydrolasesPhosphorylationPol1 Transcription Initiation Complex ProteinsSirtuinsCDC2 Protein KinaseCyclin BDNA, RibosomalPhosphoric Monoester HydrolasesPol1 Transcription Initiation Complex ProteinsSIRT7 protein, humanSirtuinstranscription factor UBF

Identifiers

PMID19174463
PMCPMC2714433
OpenAlexW2000216767

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.