Evidence map›Paper›PMID 26966248›Full record

ArticleGenes & development2016

Mte1 interacts with Mph1 and promotes crossover recombination and telomere maintenance.

Sonia Silva, Veronika Altmannova, Sarah Luke-Glaser, Peter Henriksen, Irene Gallina, Xuejiao Yang, Chunaram Choudhary, Brian Luke, Lumir Krejci, Michael Lisby

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. FANCM, BRCA1, and BLM cooperatively resolve the replication stress at the ALT telomeres.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  18. Review
  19. Article
  20. Review
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

10 authors at 3 institutions in 3 countries.

Sonia SilvaDepartment of Biology, University of Copenhagen, DK-2200 Copenhagen N, Denmark;
Veronika AltmannovaDepartment of Biology, Masaryk University, CZ-62500 Brno, Czech Republic;
Sarah Luke-GlaserInstitute of Molecular Biology gGmbH (IMB), 55128 Mainz, Germany;
Peter HenriksenThe Novo Nordisk Foundation Center for Protein Research, Faculty of Health Sciences, University of Copenhagen, DK-2200 Copenhagen N, Denmark;
Irene GallinaDepartment of Biology, University of Copenhagen, DK-2200 Copenhagen N, Denmark;
Xuejiao YangDepartment of Biology, University of Copenhagen, DK-2200 Copenhagen N, Denmark;
Chunaram ChoudharyThe Novo Nordisk Foundation Center for Protein Research, Faculty of Health Sciences, University of Copenhagen, DK-2200 Copenhagen N, Denmark;
Brian LukeInstitute of Molecular Biology gGmbH (IMB), 55128 Mainz, Germany;
Lumir KrejciDepartment of Biology, Masaryk University, CZ-62500 Brno, Czech Republic; National Centre for Biomolecular Research, Masaryk University, CZ-62500 Brno, Czech Republic; International Clinical Research Center, St. Anne's University Hospital Brno, CZ-656 91 Brno, Czech Republic; Center for Biomolecular and Cellular Engineering, St. Anne's University Hospital Brno, CZ-656 91 Brno, Czech Republic;
Michael LisbyDepartment of Biology, University of Copenhagen, DK-2200 Copenhagen N, Denmark; Center for Chromosome Stability, Department of Cellular and Molecular Medicine, University of Copenhagen, DK-2200 Copenhagen N, Denmark.ORCID http://orcid.org/0000-0002-4830-5247
University of Copenhagen · DKInstitute of Molecular Biology · DEMasaryk University · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mph1 is a member of the conserved FANCM family of DNA motor proteins that play key roles in genome maintenance processes underlying Fanconi anemia, a cancer predisposition syndrome in humans. Here, we identify Mte1 as a novel interactor of the Mph1 helicase in Saccharomyces cerevisiae. In vitro, Mte1 (Mph1-associated telomere maintenance protein 1) binds directly to DNA with a preference for branched molecules such as D loops and fork structures. In addition, Mte1 stimulates the helicase and fork regression activities of Mph1 while inhibiting the ability of Mph1 to dissociate recombination intermediates. Deletion of MTE1 reduces crossover recombination and suppresses the sensitivity of mph1Δ mutant cells to replication stress. Mph1 and Mte1 interdependently colocalize at DNA damage-induced foci and dysfunctional telomeres, and MTE1 deletion results in elongated telomeres. Taken together, our data indicate that Mte1 plays a role in regulation of crossover recombination, response to replication stress, and telomere maintenance.

Indexed as

Crossing Over, GeneticDEAD-box RNA HelicasesGene DeletionProtein TransportSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsStress, PhysiologicalTelomere-Binding ProteinsTelomere HomeostasisDEAD-box RNA HelicasesMPH1 protein, S cerevisiaeMte1 protein, S cerevisiaeSaccharomyces cerevisiae ProteinsTelomere-Binding ProteinsDNA repairgenome integrityhomologous recombinationMph1Mte1telomere maintenance

Identifiers

PMID26966248
PMCPMC4803055
OpenAlexW2295695175

What OpenQuestion holds

Textmetadata
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.