Evidence map›Paper›PMID 26012630›Full record

ArticleCytoskeleton (Hoboken, N.J.)2015

Xenopus TACC1 is a microtubule plus-end tracking protein that can regulate microtubule dynamics during embryonic development.

Christopher M Lucaj, Matthew F Evans, Belinda U Nwagbara, Patrick T Ebbert, Charlie C Baker, Joseph G Volk, Andrew F Francl, Sean P Ruvolo, Laura Anne Lowery

Open access · hybridAbstract read
In one paragraph

Article in Cytoskeleton (Hoboken, N.J.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
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  4. 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
  5. Review
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  8. 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 1 institution in 1 country.

Christopher M LucajDepartment of Biology, Boston College, 140 Commonwealth Avenue, Chestnut Hill, Massachusetts.
Matthew F EvansDepartment of Biology, Boston College, 140 Commonwealth Avenue, Chestnut Hill, Massachusetts.
Belinda U NwagbaraDepartment of Biology, Boston College, 140 Commonwealth Avenue, Chestnut Hill, Massachusetts.
Patrick T EbbertDepartment of Biology, Boston College, 140 Commonwealth Avenue, Chestnut Hill, Massachusetts.
Charlie C BakerDepartment of Biology, Boston College, 140 Commonwealth Avenue, Chestnut Hill, Massachusetts.
Joseph G VolkDepartment of Biology, Boston College, 140 Commonwealth Avenue, Chestnut Hill, Massachusetts.
Andrew F FranclDepartment of Biology, Boston College, 140 Commonwealth Avenue, Chestnut Hill, Massachusetts.
Sean P RuvoloDepartment of Biology, Boston College, 140 Commonwealth Avenue, Chestnut Hill, Massachusetts.
Laura Anne LoweryDepartment of Biology, Boston College, 140 Commonwealth Avenue, Chestnut Hill, Massachusetts.
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 family of proteins called plus-end tracking proteins (+TIPs). We recently demonstrated that the transforming acidic coiled-coil (TACC) domain family member, TACC3, can function as a +TIP to regulate microtubule dynamics in Xenopus laevis embryonic cells. Although it has been previously reported that TACC3 is the only TACC family member that exists in Xenopus, our examination of its genome determined that Xenopus, like all other vertebrates, contains three TACC family members. Here, we investigate the localization and function of Xenopus TACC1, the founding member of the TACC family. We demonstrate that it can act as a +TIP to regulate microtubule dynamics, and that the conserved C-terminal TACC domain is required for its localization to plus-ends. We also show that, in Xenopus embryonic mesenchymal cells, TACC1 and TACC3 are each required for maintaining normal microtubule growth speed but exhibit some functional redundancy in the regulation of microtubule growth lifetime. Given the conservation of TACC1 in Xenopus and other vertebrates, we propose that Xenopus laevis is a useful system to investigate unexplored cell biological functions of TACC1 and other TACC family members in the regulation of microtubule dynamics.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsCell Cycle ProteinsEmbryonic DevelopmentFemaleGreen Fluorescent ProteinsHumansMesenchymal Stem CellsMiceMicroscopy, ConfocalMicrotubule-Associated ProteinsMicrotubulesNuclear ProteinsPhenotypeProtein Structure, TertiarySoftwareCell Cycle ProteinsGreen Fluorescent ProteinsMicrotubule-Associated ProteinsNuclear ProteinsTACC1 protein, XenopusTACC3 protein, XenopusTranscription FactorsXenopus Proteinslive imagingmicrotubule dynamicsplusTipTrackertransforming acid coiled coil domainXenopus

Identifiers

PMID26012630
PMCPMC4520305
OpenAlexW1902263434

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.