Evidence map›Paper›PMID 24626187›Full record

ArticleCell cycle (Georgetown, Tex.)2014

Cdc14 targets the Holliday junction resolvase Yen1 to the nucleus in early anaphase.

Jonay García-Luis, Andrés Clemente-Blanco, Luis Aragón, Félix Machín

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

26 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
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  6. Cyclins and CDKs in the regulation of meiosis-specific events.Frontiers in cell and developmental biology · 2022
    Review
  7. Article
  8. Article
  9. International journal of molecular sciences · 2021
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. The Multiple Roles of the Cdc14 Phosphatase in Cell Cycle Control.International journal of molecular sciences · 2020
    Review
  15. Review
  16. Review
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  18. Review
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  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

4 authors at 3 institutions in 2 countries.

Jonay García-LuisGenomic Instability & Cancer Group; Unidad de Investigación; Hospital Universitario Nuestra Señora de Candelaria; Santa Cruz de Tenerife, Spain.
Andrés Clemente-BlancoCell Cycle Group; MRC Clinical Sciences Centre; Imperial College London; London, UK.
Luis AragónCell Cycle Group; MRC Clinical Sciences Centre; Imperial College London; London, UK.
Félix MachínGenomic Instability & Cancer Group; Unidad de Investigación; Hospital Universitario Nuestra Señora de Candelaria; Santa Cruz de Tenerife, Spain.
Unidad de Investigación en cuidados y servicios de salud (Investén-isciii) · ESMRC Clinical Trials Unit at UCL · GBMRC London Institute of Medical Sciences · GB

Funding

Medical Research Council MC_U120074328
6 · The paper itself

Abstract

The only canonical Holliday junction (HJ) resolvase identified in eukaryotes thus far is Yen1/GEN1. Nevertheless, Yen1/GEN1 appears to have a minor role in HJ resolution, and, instead, other structure-specific endonucleases (SSE) that recognize branched DNA play the leading roles, Mus81-Mms4/EME1 being the most important in budding yeast. Interestingly, cells tightly regulate the activity of each HJ resolvase during the yeast cell cycle. Thus, Mus81-Mms4 is activated in G 2/M, while Yen1 gets activated shortly afterwards. Nevertheless, cytological studies have shown that Yen1 is sequestered out of the nucleus when cyclin-dependent kinase activity is high, i.e., all of the cell cycle but G 1. We here show that the mitotic master phosphatase Cdc14 targets Yen1 to the nucleus in early anaphase through the FEAR network. We will further show that this FEAR-mediated Cdc14-driven event is sufficient to back-up Mus81-Mms4 in removing branched DNA structures, which are especially found in the long chromosome arms upon replication stress. Finally, we found that MEN-driven Cdc14 re-activation in late anaphase is essential to keep Yen1 in the nucleus until the next G 1. Our results highlight the essential role that early-activated Cdc14, i.e., through the FEAR network, has in removing all kind of non-proteinaceous linkages that preclude faithful sister chromatid segregation in anaphase. In addition, our results support the general idea of Yen1 acting as a last resource endonuclease to deal with any remaining HJ that might compromise genetic stability during chromosome segregation.

Indexed as

AnaphaseCell Cycle ProteinsCell NucleusDNA-Binding ProteinsEndonucleasesEpistasis, GeneticFlap EndonucleasesG2 Phase Cell Cycle CheckpointsHolliday Junction ResolvasesHumansProtein Tyrosine PhosphatasesSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsCDC14 protein, S cerevisiaeCell Cycle ProteinsDNA-Binding ProteinsEndonucleasesFlap EndonucleasesHolliday Junction ResolvasesMMS4 protein, S cerevisiaeMUS81 protein, S cerevisiaeProtein Tyrosine PhosphatasesSaccharomyces cerevisiae ProteinsYen1 protein, S cerevisiaeanaphaseCdc14Holliday junctionMMSMus81-Mms4Saccharomyces cerevisiaeYen1

Identifiers

PMID24626187
PMCPMC4050137
OpenAlexW2074459903

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.