Evidence map›Paper›PMID 41683788›Full record

ArticleInternational journal of molecular sciences2026

The Chromatin Protein CFDP1 Activates TPX2 and Promotes Chromosomal Microtubule Nucleation and Spindle Assembly.

Gokul Gopinathan, Xianghong Luan, Thomas G H Diekwisch

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Gokul GopinathanSchool of Medicine and Dentistry, University of Rochester, Rochester, NY 14642, USA.
Xianghong LuanSchool of Medicine and Dentistry, University of Rochester, Rochester, NY 14642, USA.
Thomas G H DiekwischSchool of Medicine and Dentistry, University of Rochester, Rochester, NY 14642, USA.ORCID 0000-0003-3356-9677

Funding

CP 27 GENE FUNCTION IN TOOTH DEVELOPMENTR01DE013095 · NIDCR · UNIVERSITY OF ILLINOIS AT CHICAGO · PI DIEKWISCH, THOMAS G.H. · 2001 to 2004
$1.1M
NIDCR NIH HHS DE13095NIDCR NIH HHS R01 DE013095
6 · The paper itself

Abstract

Microtubule-associated proteins (MAPs) are multifunctional tubulin-binding proteins that contribute to essential aspects of mitotic spindle formation. In the present study, loss of the MAP CFDP1 in mice resulted in gastrulation defects and embryonic lethality at e8.5 due to chromosome segregation spindle defects and loss of K-fiber stability. CFDP1 decreased the association of the nuclear transport protein importin α with the essential spindle assembly factor TPX2, thereby promoting Aurora A kinase activation, microtubule nucleation and spindle assembly. Further defining the CFDP1 mode of action, we identified CFDP1 as a bipartite molecule with an acidic N-terminus that harbors a nuclear localization signal essential for importin α dissociation from TPX2 and a basic C-terminus that interacts with tubulin, co-localizes with the mitotic spindle, and promotes microtubule bundling and polymerization. Together, our studies have established CFDP1 as an essential bipartite MAP involved in chromosomal microtubule nucleation in conjunction with TPX2 and Aurora A while also facilitating nuclear TPX2 activation through importin α dissociation.

Indexed as

Cell Cycle ProteinsMicrotubule-Associated ProteinsMicrotubulesNuclear ProteinsSpindle Apparatusalpha KaryopherinsAnimalsAurora Kinase AChromatinHumansMiceTubulinalpha KaryopherinsAurora Kinase ACell Cycle ProteinsChromatinMicrotubule-Associated ProteinsNuclear ProteinsTPX2 protein, mouseTubulinCFDP1K-fibersmicrotubule nucleationspindleTPX2

Identifiers

PMID41683788
PMCPMC12898535

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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.