Evidence map›Paper›PMID 19369413›Full record

ArticleMolecular biology of the cell2009

Functional overlap of microtubule assembly factors in chromatin-promoted spindle assembly.

Aaron C Groen, Thomas J Maresca, Jesse C Gatlin, Edward D Salmon, Timothy J Mitchison

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

23 citing papers in PubMed, 40 citations in OpenAlex.

  1. Modulation of the cytoskeleton for cancer therapy.Frontiers in cell and developmental biology · 2025
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  18. Augmin promotes meiotic spindle formation and bipolarity in Xenopus egg extracts.Proceedings of the National Academy of Sciences of the United States of America · 2011
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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

5 authors at 2 institutions in 1 country.

Aaron C GroenSystems Biology Department, Harvard Medical School, Boston, MA 02445, USA. aaron_groen@student.hms.harvard.edu
Thomas J Maresca
Jesse C Gatlin
Edward D Salmon
Timothy J Mitchison
University of North Carolina at Chapel Hill · USMarine Biological Laboratory · US

Funding

SMART ASSAYS FOR LIGANDS TO STUDY AND TREAT CANCERP01CA078048 · NCI · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI TALLARICO, JOHN A · 1998 to 2008
$16.6M
MECHANISMS OF MITOTIC SPINDLE ASSEMBLY AND FUNCTIONR37GM024364 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SALMON, EDWARD D. · 2004 to 2013
$4.1M
MECHANISMS OF MITOTIC SPINDLE ASSEMBLY AND FUNCTIONR01GM024364 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BLOOM, KERRY S, SALMON, EDWARD D. · 1985 to 2018
$3.1M
Intrinsic Spindle Mechanisms to Insure BipolarityF32GM080049 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI GATLIN, JESSE C · 2007 to 2008
$75k
NCI NIH HHS CA078048-09NCI NIH HHS P01 CA078048NIGMS NIH HHS F32 GM080049NIGMS NIH HHS GM24364NIGMS NIH HHS R01 GM024364NIGMS NIH HHS R37 GM024364
6 · The paper itself

Abstract

Distinct pathways from centrosomes and chromatin are thought to contribute in parallel to microtubule nucleation and stabilization during animal cell mitotic spindle assembly, but their full mechanisms are not known. We investigated the function of three proposed nucleation/stabilization factors, TPX2, gamma-tubulin and XMAP215, in chromatin-promoted assembly of anastral spindles in Xenopus laevis egg extract. In addition to conventional depletion-add back experiments, we tested whether factors could substitute for each other, indicative of functional redundancy. All three factors were required for microtubule polymerization and bipolar spindle assembly around chromatin beads. Depletion of TPX2 was partially rescued by the addition of excess XMAP215 or EB1, or inhibiting MCAK (a Kinesin-13). Depletion of either gamma-tubulin or XMAP215 was partially rescued by adding back XMAP215, but not by adding any of the other factors. These data reveal functional redundancy between specific assembly factors in the chromatin pathway, suggesting individual proteins or pathways commonly viewed to be essential may not have entirely unique functions.

Indexed as

AnimalsCell Cycle ProteinsChromatinFemaleGreen Fluorescent ProteinsHumansKinesinsKineticsMicroscopy, FluorescenceMicrotubule-Associated ProteinsMicrotubulesNuclear ProteinsOocytesPhosphoproteinsSpindle ApparatusTime FactorsCell Cycle ProteinsChromatinCKAP5 protein, XenopusGreen Fluorescent ProteinsKinesinsMicrotubule-Associated ProteinsNuclear ProteinsPhosphoproteinsTPX2 protein, humanTPX2 protein, XenopusTubulinXenopus Proteins

Identifiers

PMID19369413
PMCPMC2688555
OpenAlexW2132847487

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.