Evidence map›Paper›PMID 24631283›Full record

ArticleMolecular cell2014

The Cdk/cDc14 module controls activation of the Yen1 holliday junction resolvase to promote genome stability.

Christie L Eissler, Gerard Mazón, Brendan L Powers, Sergey N Savinov, Lorraine S Symington, Mark C Hall

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

60 citing papers in PubMed, 92 citations in OpenAlex.

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  12. Cyclins and CDKs in the regulation of meiosis-specific events.Frontiers in cell and developmental biology · 2022
    Review
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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 3 institutions in 1 country.

Christie L EisslerDepartment of Biochemistry, Purdue University, West Lafayette, IN 47907, USA; Center for Cancer Research, Purdue University, West Lafayette, IN 47907, USA.
Gerard MazónDepartment of Microbiology and Immunology, Columbia University Medical Center, New York, NY 10032, USA.
Brendan L PowersDepartment of Biochemistry, Purdue University, West Lafayette, IN 47907, USA; Center for Cancer Research, Purdue University, West Lafayette, IN 47907, USA.
Sergey N SavinovCenter for Cancer Research, Purdue University, West Lafayette, IN 47907, USA.
Lorraine S SymingtonDepartment of Microbiology and Immunology, Columbia University Medical Center, New York, NY 10032, USA.
Mark C HallDepartment of Biochemistry, Purdue University, West Lafayette, IN 47907, USA; Center for Cancer Research, Purdue University, West Lafayette, IN 47907, USA. Electronic address: mchall@purdue.edu.
Purdue University West Lafayette · USColumbia University Irving Medical Center · USCenter for Cancer Research · US

Funding

Mechanisms of Homologous Recombination in YeastR01GM041784 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI SYMINGTON, LORRAINE S · 1989 to 2017
$7.8M
Break-induced replication and genome rearrangementsR01GM094386 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SYMINGTON, LORRAINE S · 2010 to 2017
$2.4M
NIGMS NIH HHS R01 GM041784NIGMS NIH HHS R01 GM094386
6 · The paper itself

Abstract

Faithful genome transmission during cell division requires precise, coordinated action of DNA metabolic enzymes, including proteins responsible for DNA damage detection and repair. Dynamic phosphorylation plays an important role in controlling repair enzymes during the DNA damage response (DDR). Cdc14 phosphatases oppose cyclin-dependent kinase (Cdk) phosphorylation and have been implicated in the DDR in several model systems. Here, we have refined the substrate specificity of budding yeast Cdc14 and, using this insight, identified the Holliday junction resolvase Yen1 as a DNA repair target of Cdc14. Cdc14 activation at anaphase triggers nuclear accumulation and enzymatic activation of Yen1, likely to resolve persistent recombinational repair intermediates. Consistent with this, expression of a phosphomimetic Yen1 mutant increased sister chromatid nondisjunction. In contrast, lack of Cdk phosphorylation resulted in constitutive activity and elevated crossover-associated repair. The precise timing of Yen1 activation, governed by core cell-cycle regulators, helps coordinate DNA repair with chromosome segregation and safeguards against genome destabilization.

Indexed as

Genomic InstabilityCDC2 Protein KinaseCell Cycle ProteinsChromosome SegregationChromosomes, FungalCyclin-Dependent KinasesDNA RepairEnzyme ActivationGene Expression Regulation, EnzymologicGene Expression Regulation, FungalHolliday Junction ResolvasesMitosisMutationPhosphorylationProtein Tyrosine PhosphatasesRecombination, GeneticCDC14 protein, S cerevisiaeCDC2 Protein KinaseCell Cycle ProteinsCyclin-Dependent KinasesHolliday Junction ResolvasesProtein Tyrosine PhosphatasesSaccharomyces cerevisiae ProteinsYen1 protein, S cerevisiae

Identifiers

PMID24631283
PMCPMC3988236
OpenAlexW1987005978

What OpenQuestion holds

Textmetadata
LicenceTDM
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.