Evidence map›Paper›PMID 25187649›Full record

ArticleMolecular biology of the cell2014

TACC3 is a microtubule plus end-tracking protein that promotes axon elongation and also regulates microtubule plus end dynamics in multiple embryonic cell types.

Belinda U Nwagbara, Anna E Faris, Elizabeth A Bearce, Burcu Erdogan, Patrick T Ebbert, Matthew F Evans, Erin L Rutherford, Tiffany B Enzenbacher, Laura Anne Lowery

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

39 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
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  4. Gcap14 is a microtubule plus-end-tracking protein coordinating microtubule-actin crosstalk during neurodevelopment.Proceedings of the National Academy of Sciences of the United States of America · 2023
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  16. Characterization of Xenopus laevis guanine deaminase reveals new insights for its expression and function in the embryonic kidney.Developmental dynamics : an official publication of the American Association of Anatomists · 2019
    Article
  17. Article
  18. Molecular basis of the functions of the mammalian neuronal growth cone revealed using new methods.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2019
    Review
  19. The Many Faces ofFrontiers in physiology · 2019
    Article
  20. 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

9 authors at 1 institution in 1 country.

Belinda U NwagbaraDepartment of Biology, Boston College, Chestnut Hill, MA 02467.
Anna E FarisDepartment of Biology, Boston College, Chestnut Hill, MA 02467.
Elizabeth A BearceDepartment of Biology, Boston College, Chestnut Hill, MA 02467.
Burcu ErdoganDepartment of Biology, Boston College, Chestnut Hill, MA 02467.
Patrick T EbbertDepartment of Biology, Boston College, Chestnut Hill, MA 02467.
Matthew F EvansDepartment of Biology, Boston College, Chestnut Hill, MA 02467.
Erin L RutherfordDepartment of Biology, Boston College, Chestnut Hill, MA 02467.
Tiffany B EnzenbacherDepartment of Biology, Boston College, Chestnut Hill, MA 02467.
Laura Anne LoweryDepartment of Biology, Boston College, Chestnut Hill, MA 02467 Laura.lowery@bc.edu.
Boston College · US

Funding

Function of Microtubule Plus-End-Tracking Proteins in the Neuronal Growth ConeR00MH095768 · NIMH · BOSTON COLLEGE · PI LOWERY, LAURA ANNE · 2014 to 2016
$747k
NIMH NIH HHS R00 MH095768
6 · The paper itself

Abstract

Microtubule plus end dynamics are regulated by a conserved family of proteins called plus end-tracking proteins (+TIPs). It is unclear how various +TIPs interact with each other and with plus ends to control microtubule behavior. The centrosome-associated protein TACC3, a member of the transforming acidic coiled-coil (TACC) domain family, has been implicated in regulating several aspects of microtubule dynamics. However, TACC3 has not been shown to function as a +TIP in vertebrates. Here we show that TACC3 promotes axon outgrowth and regulates microtubule dynamics by increasing microtubule plus end velocities in vivo. We also demonstrate that TACC3 acts as a +TIP in multiple embryonic cell types and that this requires the conserved C-terminal TACC domain. Using high-resolution live-imaging data on tagged +TIPs, we show that TACC3 localizes to the extreme microtubule plus end, where it lies distal to the microtubule polymerization marker EB1 and directly overlaps with the microtubule polymerase XMAP215. TACC3 also plays a role in regulating XMAP215 stability and localizing XMAP215 to microtubule plus ends. Taken together, our results implicate TACC3 as a +TIP that functions with XMAP215 to regulate microtubule plus end dynamics.

Indexed as

AnimalsAxonsEmbryo Culture TechniquesEmbryo, NonmammalianGrowth ConesInterphaseMicrotubule-Associated ProteinsMicrotubulesProtein StabilityProtein Structure, TertiaryTranscription FactorsXenopus laevisXenopus ProteinsCKAP5 protein, XenopusMicrotubule-Associated ProteinsTACC3 protein, XenopusTranscription FactorsXenopus Proteins

Identifiers

PMID25187649
PMCPMC4214782
OpenAlexW1996184123

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.