Evidence map›Paper›PMID 24470217›Full record

ArticleG3 (Bethesda, Md.)2014

The yeast Ess1 prolyl isomerase controls Swi6 and Whi5 nuclear localization.

David Atencio, Cassandra Barnes, Thomas M Duncan, Ian M Willis, Steven D Hanes

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Prolyl isomerases in gene transcription.Biochimica et biophysica acta · 2015
    Review
  8. 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

5 authors at 2 institutions in 1 country.

David AtencioDepartment of Biochemistry and Molecular Biology, SUNY Upstate Medical University, Syracuse, New York 13210.
Cassandra Barnes
Thomas M Duncan
Ian M Willis
Steven D Hanes
SUNY Upstate Medical University · USAlbert Einstein College of Medicine · US

Funding

Yeast Ess1, a Conserved PPlase Essential for MitosisR01GM055108 · NIGMS · WADSWORTH CENTER · PI HANES, STEVEN D. · 1997 to 2010
$2.5M
Transcriptional Repression by Maf1 in YeastR01GM085177 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI WILLIS, IAN M · 2009 to 2012
$2.1M
Energy Coupling and Regulation in the ATP Synthase of E. coliR01GM083088 · NIGMS · UPSTATE MEDICAL UNIVERSITY · PI DUNCAN, THOMAS M · 2009 to 2012
$1.6M
NIGMS NIH HHS GM055108NIGMS NIH HHS GM083088NIGMS NIH HHS GM085177NIGMS NIH HHS R01 GM055108NIGMS NIH HHS R01 GM083088NIGMS NIH HHS R01 GM085177
6 · The paper itself

Abstract

The Ess1 prolyl isomerase from Saccharomyces cerevisiae and its human ortholog, Pin1, play critical roles in transcription by regulating RNA polymerase II. In human cells, Pin1 also regulates a variety of signaling proteins, and Pin1 misexpression is linked to several human diseases. To gain insight into Ess1/Pin1 function, we carried out a synthetic genetic array screen to identify novel targets of Ess1 in yeast. We identified potential targets of Ess1 in transcription, stress, and cell-cycle pathways. We focused on the cell-cycle regulators Swi6 and Whi5, both of which show highly regulated nucleocytoplasmic shuttling during the cell cycle. Surprisingly, Ess1 did not control their transcription but instead was necessary for their nuclear localization. Ess1 associated with Swi6 and Whi5 in vivo and bound directly to peptides corresponding to their nuclear localization sequences in vitro. Binding by Ess1 was significant only if the Swi6 and Whi5 peptides were phosphorylated at Ser-Pro motifs, the target sites of cyclin-dependent kinases. On the basis of these results, we propose a model in which Ess1 induces a conformational switch (cis-trans isomerization) at phospho-Ser-Pro sites within the nuclear targeting sequences of Swi6 and Whi5. This switch would promote nuclear entry and/or retention during late M and G1 phases and might work by stimulating dephosphorylation at these sites by the Cdc14 phosphatase. This is the first study to identify targets of Ess1 in yeast other than RNA polymerase II.

Indexed as

Amino Acid SequenceCell Cycle ProteinsCell DivisionCell NucleusG1 PhaseKineticsModels, MolecularMolecular Sequence DataNIMA-Interacting Peptidylprolyl IsomerasePeptidylprolyl IsomerasePhosphorylationProtein BindingProtein Tyrosine PhosphatasesRepressor ProteinsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsCDC14 protein, S cerevisiaeCell Cycle ProteinsESS1 protein, S cerevisiaeNIMA-Interacting Peptidylprolyl IsomerasePeptidylprolyl IsomerasePIN1 protein, humanProtein Tyrosine PhosphatasesRepressor ProteinsSaccharomyces cerevisiae ProteinsSWI6 protein, S cerevisiaeTranscription FactorsWhi5 protein, S cerevisiaebiolayer interferometrycyclin-dependent kinase sitesnuclear importproline isomerase

Identifiers

PMID24470217
PMCPMC3962490
OpenAlexW2139504027

What OpenQuestion holds

Textmetadata
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.