Evidence map›Paper›PMID 23449222›Full record

ArticleNucleic acids research2013

Human SIRT1 regulates DNA binding and stability of the Mcm10 DNA replication factor via deacetylation.

Samuel T Fatoba, Silvia Tognetti, Melissa Berto, Elisabetta Leo, Claire M Mulvey, Jasminka Godovac-Zimmermann, Yves Pommier, Andrei L Okorokov

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

22 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Review
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  7. Article
  8. Article
  9. Control of DNA replication timing in the 3D genome.Nature reviews. Molecular cell biology · 2019
    Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Sirtuins in epigenetic regulation.Chemical reviews · 2015
    Review
  18. Article
  19. MCM10: one tool for all-Integrity, maintenance and damage control.Seminars in cell & developmental biology · 2014
    Review
  20. 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

8 authors at 4 institutions in 2 countries.

Samuel T FatobaWolfson Institute for Biomedical Research, University College London, Gower Street, London WC1E 6BT, UK.
Silvia Tognetti
Melissa Berto
Elisabetta Leo
Claire M Mulvey
Jasminka Godovac-Zimmermann
Yves Pommier
Andrei L Okorokov
National Institutes of Health · USUniversity College London · GBNational Cancer Institute · USRoland Hill (United Kingdom) · GB

Funding

DNA Repair, Cell Cycle Checkpoints and Apoptosis as Targets for Anticancer DrugsZIABC006150 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI POMMIER, YVES · 2009 to 2025
$23.0M
PROTEIN-ASSOCIATED DNA BREAKS AS INDICATOR OF TOPOISOMERASE INHIBITIONZ01BC006150 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI POMMIER, YVES · 1996 to 2008
$1.5M
Intramural NIH HHSMedical Research Council G0700001NCI NIH HHS Z01 BC 006150-19LMPWellcome Trust 081879
6 · The paper itself

Abstract

The eukaryotic DNA replication initiation factor Mcm10 is essential for both replisome assembly and function. Human Mcm10 has two DNA-binding domains, the conserved internal domain (ID) and the C-terminal domain (CTD), which is specific to metazoans. SIRT1 is a nicotinamide adenine dinucleotide (NAD)-dependent deacetylase that belongs to the sirtuin family. It is conserved from yeast to human and participates in cellular controls of metabolism, longevity, gene expression and genomic stability. Here we report that human Mcm10 is an acetylated protein regulated by SIRT1, which binds and deacetylates Mcm10 both in vivo and in vitro, and modulates Mcm10 stability and ability to bind DNA. Mcm10 and SIRT1 appear to act synergistically for DNA replication fork initiation. Furthermore, we show that the two DNA-binding domains of Mcm10 are modulated in distinct fashion by acetylation/deacetylation, suggesting an integrated regulation mechanism. Overall, our study highlights the importance of protein acetylation for DNA replication initiation and progression, and suggests that SIRT1 may mediate a crosstalk between cellular circuits controlling metabolism and DNA synthesis.

Indexed as

AcetylationCell CycleCell Cycle ProteinsCell LineChromatinDNA ReplicationHumansMinichromosome Maintenance ProteinsProtein BindingProtein Interaction Domains and MotifsProtein StabilityReplication OriginSirtuin 1Cell Cycle ProteinsChromatinMCM10 protein, humanMinichromosome Maintenance ProteinsSIRT1 protein, humanSirtuin 1

Identifiers

PMID23449222
PMCPMC3627603
OpenAlexW2138874139

What OpenQuestion holds

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LicenceCC BY-NC
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.