Evidence map›Paper›PMID 25324523›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

A nontranscriptional role for Oct4 in the regulation of mitotic entry.

Rui Zhao, Richard W Deibler, Paul H Lerou, Andrea Ballabeni, Garrett C Heffner, Patrick Cahan, Juli J Unternaehrer, Marc W Kirschner, George Q Daley

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

27 citing papers in PubMed, 42 citations in OpenAlex.

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  18. Cycling to Meet Fate: Connecting Pluripotency to the Cell Cycle.Frontiers in cell and developmental biology · 2018
    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

9 authors at 4 institutions in 1 country.

Rui ZhaoStem Cell Transplantation Program, Division of Pediatric Hematology/Oncology, Manton Center for Orphan Disease Research, Boston Children's Hospital, Dana-Farber Cancer Institute, Department of Biological Chemistry and Molecular Pharmacology, Harvard Stem Cell Institute, and Howard Hughes Medical Institute, Harvard Medical School, Boston, MA 02115;
Richard W DeiblerDepartment of Systems Biology, Harvard Medical School, Boston, MA 02115; and.
Paul H LerouDepartment of Newborn Medicine and Department of Medicine, Division of Genetics, Brigham & Women's Hospital, Department of Medicine, Division of Newborn Medicine, Boston Children's Hospital, and Harvard Stem Cell Institute, Harvard Medical School, Boston, MA 02115.
Andrea BallabeniDepartment of Systems Biology, Harvard Medical School, Boston, MA 02115; and.
Garrett C HeffnerStem Cell Transplantation Program, Division of Pediatric Hematology/Oncology, Manton Center for Orphan Disease Research, Boston Children's Hospital, Dana-Farber Cancer Institute, Department of Biological Chemistry and Molecular Pharmacology, Harvard Stem Cell Institute, and Howard Hughes Medical Institute, Harvard Medical School, Boston, MA 02115;
Patrick CahanStem Cell Transplantation Program, Division of Pediatric Hematology/Oncology, Manton Center for Orphan Disease Research, Boston Children's Hospital, Dana-Farber Cancer Institute, Department of Biological Chemistry and Molecular Pharmacology, Harvard Stem Cell Institute, and Howard Hughes Medical Institute, Harvard Medical School, Boston, MA 02115;
Juli J UnternaehrerStem Cell Transplantation Program, Division of Pediatric Hematology/Oncology, Manton Center for Orphan Disease Research, Boston Children's Hospital, Dana-Farber Cancer Institute, Department of Biological Chemistry and Molecular Pharmacology, Harvard Stem Cell Institute, and Howard Hughes Medical Institute, Harvard Medical School, Boston, MA 02115;
Marc W KirschnerDepartment of Systems Biology, Harvard Medical School, Boston, MA 02115; and marc@hms.harvard.edu george.daley@childrens.harvard.edu.
George Q DaleyStem Cell Transplantation Program, Division of Pediatric Hematology/Oncology, Manton Center for Orphan Disease Research, Boston Children's Hospital, Dana-Farber Cancer Institute, Department of Biological Chemistry and Molecular Pharmacology, Harvard Stem Cell Institute, and Howard Hughes Medical Institute, Harvard Medical School, Boston, MA 02115; marc@hms.harvard.edu george.daley@childrens.harvard.edu.
Harvard University · USBoston Children's Hospital · USCenter for Systems Biology · USDana-Farber Cancer Institute · US

Funding

SYNAPTIC MECHANISMS IN HIPPOCAMPAL EPILEPTOGENESISP30HD018655 · NICHD · CHILDREN'S HOSPITAL BOSTON · PI POMEROY, SCOTT LOREN · 1985 to 2015
$26.2M
BIOCHEMICAL STUDIES OF MITOSISR01GM026875 · NIGMS · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI KIRSCHNER, MARC WALLACE · 1985 to 2019
$18.2M
Customized stem cells for clinical application in blood disordersR24DK092760 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI COLLINS, JAMES J, DALEY, GEORGE Q · 2011 to 2018
$10.7M
CELL CYCLE REGULATIONR01GM039023 · NIGMS · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI KIRSCHNER, MARC WALLACE · 1988 to 2017
$10.2M
Human Pluripotent Stem Cell and Progenitor Models of Cardiac and Blood DiseasesU01HL100001 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI DALEY, GEORGE Q, ORKIN, STUART H · 2009 to 2015
$8.9M
TRAINING PROGRAM IN MOLECULAR HEMATOLOGYT32HL007623 · NHLBI · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI HANDIN, ROBERT I · 1985 to 2010
$7.0M
Progenitor Cells inHuman Skeletal MuscleP50NS040828 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI GUSSONI, EMANUELA · 2008 to 2011
$5.9M
Quantifying post-translational modifications and protein expression by HTP-MSRC4GM096319 · NIGMS · HARVARD MEDICAL SCHOOL · PI KIRSCHNER, MARC WALLACE · 2010 to 2010
$3.8M
Genomic stability of human pluripotent stem cellsK99HD061981 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI LEROU, PAUL HUBERT · 2009 to 2009
$97k
Howard Hughes Medical InstituteNHLBI NIH HHS T32 HL007623NHLBI NIH HHS T32HL007623NHLBI NIH HHS U01 HL100001NHLBI NIH HHS UO1-HL100001NICHD NIH HHS K99 HD061981NICHD NIH HHS K99HD061981NICHD NIH HHS NIH-P30-HD18655NICHD NIH HHS P30 HD018655NIDDK NIH HHS R24 DK092760NIDDK NIH HHS R24DK092760NIGMS NIH HHS R01 GM026875NIGMS NIH HHS R01GM026875NIGMS NIH HHS R01 GM039023NIGMS NIH HHS R01GM039023NIGMS NIH HHS RC4 GM096319NIGMS NIH HHS RC4GM096319NINDS NIH HHS NIH-P50-NS40828NINDS NIH HHS P50 NS040828
6 · The paper itself

Abstract

Rapid progression through the cell cycle and a very short G1 phase are defining characteristics of embryonic stem cells. This distinct cell cycle is driven by a positive feedback loop involving Rb inactivation and reduced oscillations of cyclins and cyclin-dependent kinase (Cdk) activity. In this setting, we inquired how ES cells avoid the potentially deleterious consequences of premature mitotic entry. We found that the pluripotency transcription factor Oct4 (octamer-binding transcription factor 4) plays an unappreciated role in the ES cell cycle by forming a complex with cyclin-Cdk1 and inhibiting Cdk1 activation. Ectopic expression of Oct4 or a mutant lacking transcriptional activity recapitulated delayed mitotic entry in HeLa cells. Reduction of Oct4 levels in ES cells accelerated G2 progression, which led to increased chromosomal missegregation and apoptosis. Our data demonstrate an unexpected nontranscriptional function of Oct4 in the regulation of mitotic entry.

Indexed as

AnimalsCDC2 Protein KinaseCyclin-Dependent KinasesCyclinsEmbryonic Stem CellsEnzyme ActivationG1 PhaseG2 PhaseHeLa CellsHumansMiceOctamer Transcription Factor-3Retinoblastoma ProteinCDC2 Protein KinaseCDK1 protein, humanCyclin-Dependent KinasesCyclinsOctamer Transcription Factor-3POU5F1 protein, humanPou5f1 protein, mouseRetinoblastoma ProteinCDC25Cdk1mitotic entryOct4pluripotent stem cells

Identifiers

PMID25324523
PMCPMC4226071
OpenAlexW2103077039

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.