Evidence map›Paper›PMID 26582917›Full record

ArticleNucleic acids research2016

Mcm10 coordinates the timely assembly and activation of the replication fork helicase.

Patricia Perez-Arnaiz, Irina Bruck, Daniel L Kaplan

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2016. 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
2.6field-weighted citation impact, top 10% 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
  3. Article
  4. Article
  5. Article
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  7. Article
  8. Article
  9. Single-molecule visualization ofProceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  10. Article
  11. Article
  12. Article
  13. Eukaryotic DNA Replication Fork.Annual review of biochemistry · 2017
    Review
  14. The RecJ2 protein in the thermophilic archaeonThe Journal of biological chemistry · 2017
    Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Mapping ubiquitination sites ofBiochemistry and biophysics reports · 2016
    Article
  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

3 authors at 1 institution in 1 country.

Patricia Perez-ArnaizFlorida State University College of Medicine, Department of Biomedical Sciences, Tallahassee, FL 32306, USA.
Irina BruckFlorida State University College of Medicine, Department of Biomedical Sciences, Tallahassee, FL 32306, USA.
Daniel L KaplanFlorida State University College of Medicine, Department of Biomedical Sciences, Tallahassee, FL 32306, USA Daniel.Kaplan@med.fsu.edu.
Florida State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mcm10 is an essential replication factor that is required for DNA replication in eukaryotes. Two key steps in the initiation of DNA replication are the assembly and activation of Cdc45-Mcm2-7-GINS (CMG) replicative helicase. However, it is not known what coordinates helicase assembly with helicase activation. We show in this manuscript, using purified proteins from budding yeast, that Mcm10 directly interacts with the Mcm2-7 complex and Cdc45. In fact, Mcm10 recruits Cdc45 to Mcm2-7 complex in vitro. To study the role of Mcm10 in more detail in vivo we used an auxin inducible degron in which Mcm10 is degraded upon addition of auxin. We show in this manuscript that Mcm10 is required for the timely recruitment of Cdc45 and GINS recruitment to the Mcm2-7 complex in vivo during early S phase. We also found that Mcm10 stimulates Mcm2 phosphorylation by DDK in vivo and in vitro. These findings indicate that Mcm10 plays a critical role in coupling replicative helicase assembly with helicase activation. Mcm10 is first involved in the recruitment of Cdc45 to the Mcm2-7 complex. After Cdc45-Mcm2-7 complex assembly, Mcm10 promotes origin melting by stimulating DDK phosphorylation of Mcm2, which thereby leads to GINS attachment to Mcm2-7.

Indexed as

DNA ReplicationCell Cycle ProteinsCell ProliferationDNA-Binding ProteinsDNA HelicasesMinichromosome Maintenance ProteinsMultiprotein ComplexesPhosphorylationProtein BindingReplication OriginCell Cycle ProteinsDNA-Binding ProteinsDNA HelicasesMinichromosome Maintenance ProteinsMultiprotein Complexes

Identifiers

PMID26582917
PMCPMC4705653
OpenAlexW2177517030

What OpenQuestion holds

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LicenceCC BY
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.