Evidence map›Paper›PMID 31897425›Full record

ArticleScience advances2019

ATAT1-enriched vesicles promote microtubule acetylation via axonal transport.

Aviel Even, Giovanni Morelli, Loïc Broix, Chiara Scaramuzzino, Silvia Turchetto, Ivan Gladwyn-Ng, Romain Le Bail, Michal Shilian, Stephen Freeman, Maria M Magiera and 10 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

41 citing papers in PubMed, 71 citations in OpenAlex.

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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

20 authors at 6 institutions in 4 countries.

Aviel EvenLaboratory for Neurodegenerative Diseases and Personalized Medicine, Department of Cell Research and Immunology, The George S. Wise Faculty for Life Sciences, Sagol School of Neurosciences, Tel Aviv University, Ramat Aviv 69978, Israel.ORCID 0000-0003-0534-4462
Giovanni MorelliGIGA-Stem Cells and GIGA-Neurosciences, Interdisciplinary Cluster for Applied Genoproteomics (GIGA-R), University of Liège, CHU Sart Tilman, Liège 4000, Belgium.ORCID 0000-0002-4002-9049
Loïc BroixGIGA-Stem Cells and GIGA-Neurosciences, Interdisciplinary Cluster for Applied Genoproteomics (GIGA-R), University of Liège, CHU Sart Tilman, Liège 4000, Belgium.ORCID 0000-0002-8231-370X
Chiara ScaramuzzinoGrenoble Institut des Neurosciences, GIN, Univ. Grenoble Alpes, F-38000 Grenoble, France.ORCID 0000-0001-9454-8701
Silvia TurchettoGIGA-Stem Cells and GIGA-Neurosciences, Interdisciplinary Cluster for Applied Genoproteomics (GIGA-R), University of Liège, CHU Sart Tilman, Liège 4000, Belgium.
Ivan Gladwyn-NgGIGA-Stem Cells and GIGA-Neurosciences, Interdisciplinary Cluster for Applied Genoproteomics (GIGA-R), University of Liège, CHU Sart Tilman, Liège 4000, Belgium.
Romain Le BailGIGA-Stem Cells and GIGA-Neurosciences, Interdisciplinary Cluster for Applied Genoproteomics (GIGA-R), University of Liège, CHU Sart Tilman, Liège 4000, Belgium.ORCID 0000-0002-2690-4214
Michal ShilianLaboratory for Neurodegenerative Diseases and Personalized Medicine, Department of Cell Research and Immunology, The George S. Wise Faculty for Life Sciences, Sagol School of Neurosciences, Tel Aviv University, Ramat Aviv 69978, Israel.ORCID 0000-0002-1486-2598
Stephen FreemanGIGA-Stem Cells and GIGA-Neurosciences, Interdisciplinary Cluster for Applied Genoproteomics (GIGA-R), University of Liège, CHU Sart Tilman, Liège 4000, Belgium.
Maria M MagieraInstitut Curie, PSL Research University, CNRS UMR 3348, F-91405 Orsay, France.ORCID 0000-0003-4847-3053
A S JijumonInstitut Curie, PSL Research University, CNRS UMR 3348, F-91405 Orsay, France.ORCID 0000-0001-8522-3438
Nathalie KrusyGIGA-Stem Cells and GIGA-Neurosciences, Interdisciplinary Cluster for Applied Genoproteomics (GIGA-R), University of Liège, CHU Sart Tilman, Liège 4000, Belgium.
Brigitte MalgrangeGIGA-Stem Cells and GIGA-Neurosciences, Interdisciplinary Cluster for Applied Genoproteomics (GIGA-R), University of Liège, CHU Sart Tilman, Liège 4000, Belgium.ORCID 0000-0002-8957-2528
Bert BroneBIOMED Research Institute, University of Hasselt, Hasselt 3500, Belgium.ORCID 0000-0002-4851-9480
Paula DietrichDepartment of Physiology, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Ioannis DragatsisDepartment of Physiology, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Carsten JankeInstitut Curie, PSL Research University, CNRS UMR 3348, F-91405 Orsay, France.ORCID 0000-0001-7053-2000
Frédéric SaudouGrenoble Institut des Neurosciences, GIN, Univ. Grenoble Alpes, F-38000 Grenoble, France.ORCID 0000-0001-6107-1046
Miguel WeilLaboratory for Neurodegenerative Diseases and Personalized Medicine, Department of Cell Research and Immunology, The George S. Wise Faculty for Life Sciences, Sagol School of Neurosciences, Tel Aviv University, Ramat Aviv 69978, Israel.ORCID 0000-0001-5721-653X
Laurent NguyenGIGA-Stem Cells and GIGA-Neurosciences, Interdisciplinary Cluster for Applied Genoproteomics (GIGA-R), University of Liège, CHU Sart Tilman, Liège 4000, Belgium.ORCID 0000-0002-8560-3008
University of Liège · BETel Aviv University · ILUniversité Paris-Sud · FRInserm · FRUniversity of Tennessee Health Science Center · USHasselt University · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microtubules are polymerized dimers of α- and β-tubulin that underlie a broad range of cellular activities. Acetylation of α-tubulin by the acetyltransferase ATAT1 modulates microtubule dynamics and functions in neurons. However, it remains unclear how this enzyme acetylates microtubules over long distances in axons. Here, we show that loss of ATAT1 impairs axonal transport in neurons in vivo, and cell-free motility assays confirm a requirement of α-tubulin acetylation for proper bidirectional vesicular transport. Moreover, we demonstrate that the main cellular pool of ATAT1 is transported at the cytosolic side of neuronal vesicles that are moving along axons. Together, our data suggest that axonal transport of ATAT1-enriched vesicles is the predominant driver of α-tubulin acetylation in axons.

Indexed as

AcetylationAcetyltransferasesAnimalsAxonal TransportDrosophila melanogasterFemaleHEK293 CellsHeLa CellsHumansInduced Pluripotent Stem CellsLarvaLocomotionMaleMiceMice, KnockoutMicrotubule ProteinsAcetyltransferasesATAT1 protein, humanATAT1 protein, mouseMicrotubule ProteinsTubulin

Identifiers

PMID31897425
PMCPMC6920029
OpenAlexW2994724123

What OpenQuestion holds

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LicenceCC BY-NC
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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.