Evidence map›Paper›PMID 27146114›Full record

ArticleMolecular biology of the cell2016

Loss of CENP-F results in distinct microtubule-related defects without chromosomal abnormalities.

Elise R Pfaltzgraff, Gretchen M Roth, Paul M Miller, Anneelizabeth G Gintzig, Ryoma Ohi, David M Bader

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.3field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 20 citations in OpenAlex.

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  15. Centromere Protein F (CENPF): A novel marker for salivary gland pathology.Journal of oral and maxillofacial pathology : JOMFP
    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

6 authors at 1 institution in 1 country.

Elise R PfaltzgraffDivision of Cardiovascular Medicine, Department of Medicine, Vanderbilt University, Nashville, TN 37232.
Gretchen M RothDivision of Cardiovascular Medicine, Department of Medicine, Vanderbilt University, Nashville, TN 37232.
Paul M MillerDivision of Cardiovascular Medicine, Department of Medicine, Vanderbilt University, Nashville, TN 37232.
Anneelizabeth G GintzigDivision of Hematology-Oncology, Department of Pediatrics, Vanderbilt University, Nashville, TN 37232.
Ryoma OhiDepartment of Cell and Developmental Biology, Vanderbilt University, Nashville, TN 37232 ryoma.ohi@vanderbilt.edu david.bader@vanderbilt.edu.
David M BaderDivision of Cardiovascular Medicine, Department of Medicine, Vanderbilt University, Nashville, TN 37232 ryoma.ohi@vanderbilt.edu david.bader@vanderbilt.edu.
Vanderbilt University · US

Funding

TRAINING GRANT IN MECHANISMS OF VASCULAR DISEASET32HL007751 · NHLBI · VANDERBILT UNIVERSITY · PI BOCK, PAUL E · 1994 to 2014
$6.6M
Training Program in Stem Cell and Regenerative Developmental BiologyT32HD007502 · NICHD · VANDERBILT UNIVERSITY · PI WRIGHT, CHRISTOPHER V · 1997 to 2022
$5.4M
REGULATION OF CARDIAC MYOCYTE DIFFERENTIATIONR01HL037675 · NHLBI · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI BADER, DAVID M · 1986 to 2017
$4.7M
Regulation of microtubule dynamics during cell divisionR01GM086610 · NIGMS · VANDERBILT UNIVERSITY · PI OHI, RYOMA · 2010 to 2023
$4.5M
NHLBI NIH HHS R01 HL037675NHLBI NIH HHS T32 HL007751NICHD NIH HHS T32 HD007502NIGMS NIH HHS R01 GM086610
6 · The paper itself

Abstract

Microtubule (MT)-binding centromere protein F (CENP-F) was previously shown to play a role exclusively in chromosome segregation during cellular division. Many cell models of CENP-F depletion show a lag in the cell cycle and aneuploidy. Here, using our novel genetic deletion model, we show that CENP-F also regulates a broader range of cellular functions outside of cell division. We characterized CENP-F(+/+) and CENP-F(-/-) mouse embryonic fibroblasts (MEFs) and found drastic differences in multiple cellular functions during interphase, including cell migration, focal adhesion dynamics, and primary cilia formation. We discovered that CENP-F(-/-) MEFs have severely diminished MT dynamics, which underlies the phenotypes we describe. These data, combined with recent biochemical research demonstrating the strong binding of CENP-F to the MT network, support the conclusion that CENP-F is a powerful regulator of MT dynamics during interphase and affects heterogeneous cell functions.

Indexed as

AnimalsCell CycleCentromereChromosomal Proteins, Non-HistoneChromosome AberrationsChromosome SegregationFibroblastsInterphaseKinetochoresMiceMice, KnockoutMicrofilament ProteinsMicrotubulesMitosisProtein Bindingcentromere protein FChromosomal Proteins, Non-HistoneMicrofilament Proteins

Identifiers

PMID27146114
PMCPMC4927273
OpenAlexW2345929719

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.