Evidence map›Paper›PMID 30355484›Full record

ArticleCell reports2018

Microtubule Acetylation Is Required for Mechanosensation in Drosophila.

Connie Yan, Fei Wang, Yun Peng, Claire R Williams, Brian Jenkins, Jill Wildonger, Hyeon-Jin Kim, Jonathan B Perr, Joshua C Vaughan, Megan E Kern and 7 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.1field-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

43 citing papers in PubMed, 75 citations in OpenAlex.

  1. Review
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  7. Review
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  9. Article
  10. Tubulin Acetylation and the Cellular Mechanosensing and Stress Response.Results and problems in cell differentiation · 2025
    Review
  11. Article
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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

17 authors at 4 institutions in 1 country.

Connie YanDepartment of Biology, University of Washington, Seattle, WA 98195, USA.
Fei WangDepartment of Neurobiology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Yun PengDepartment of Biology, University of Washington, Seattle, WA 98195, USA.
Claire R WilliamsDepartment of Biology, University of Washington, Seattle, WA 98195, USA.
Brian JenkinsDepartment of Biochemistry, University of Wisconsin-Madison, Madison, WI 53706, USA.
Jill WildongerDepartment of Biochemistry, University of Wisconsin-Madison, Madison, WI 53706, USA.
Hyeon-Jin KimDepartment of Chemistry, University of Washington, Seattle, WA 98195, USA.
Jonathan B PerrDepartment of Chemistry, University of Washington, Seattle, WA 98195, USA.
Joshua C VaughanDepartment of Chemistry, University of Washington, Seattle, WA 98195, USA; Department of Physiology and Biophysics, University of Washington, Seattle, WA 98195, USA.
Megan E KernDepartment of Physics & Astronomy, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-3280, USA.
Michael R FalvoDepartment of Physics & Astronomy, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-3280, USA.
E Timothy O'BrienDepartment of Physics & Astronomy, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-3280, USA.
Richard SuperfineDepartment of Applied and Physical Sciences, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-3280, USA.
John C TuthillDepartment of Physiology and Biophysics, University of Washington, Seattle, WA 98195, USA.
Yang XiangDepartment of Neurobiology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Stephen L RogersDepartment of Biology, Integrative Program for Biological and Genome Sciences, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-3280, USA; Lineberger Comprehensive Cancer Center, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-3280, USA. Electronic address: srogers@bio.unc.edu.
Jay Z ParrishDepartment of Biology, University of Washington, Seattle, WA 98195, USA. Electronic address: jzp2@uw.edu.
University of Washington · USUniversity of North Carolina at Chapel Hill · USUniversity of Massachusetts Chan Medical School · USUniversity of Wisconsin–Madison · US

Funding

INTERACTIVE GRAPHICS FOR MOLECULAR STUDIES &MICROSCOPYP41EB002025 · NIBIB · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SUPERFINE, RICHARD · 2003 to 2019
$16.9M
Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Annette L. Parks · 2014 to 2026
$13.5M
MOLECULAR AND CELLULAR BIOPHYSICS TRAINING PROGRAMT32GM008570 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KUHLMAN, BRIAN A, SLEP, KEVIN C · 1995 to 2022
$5.1M
Structural and functional coupling of epidermis to somatosensory neurons in DrosophilaR01NS076614 · NINDS · UNIVERSITY OF WASHINGTON · PI BAUTISTA, DIANA MICHELE, PARRISH, JAY Z · 2011 to 2023
$4.2M
Spatially Resolved Transcriptomics Enabled by Ultrabright Pdot Probes for Interrogation of Complex TissuesR01MH115767 · NIMH · UNIVERSITY OF WASHINGTON · PI CHIU, DANIEL T, VAUGHAN, JOSHUA · 2017 to 2021
$3.7M
Molecular Mechanisms of nociceptor sensitizationR01NS089787 · NINDS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI XIANG, YANG · 2015 to 2019
$1.8M
Cellular and molecular mechanisms underlying neuronal activity-controlled regeneration specificityR21NS107924 · NINDS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI XIANG, YANG · 2018 to 2019
$481k
Multi-scale analysis and modeling of acetylation effects on neuronal microtubulesR21NS101553 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI GARDNER, MELISSA, WILDONGER, JILL C · 2017 to 2018
$422k
NIBIB NIH HHS P41 EB002025NIGMS NIH HHS T32 GM008570NIH HHS P40 OD018537NIMH NIH HHS R01 MH115767NINDS NIH HHS R01 NS076614NINDS NIH HHS R01 NS089787NINDS NIH HHS R21 NS101553NINDS NIH HHS R21 NS107924
6 · The paper itself

Abstract

At the cellular level, α-tubulin acetylation alters the structure of microtubules to render them mechanically resistant to compressive forces. How this biochemical property of microtubule acetylation relates to mechanosensation remains unknown, although prior studies have shown that microtubule acetylation influences touch perception. Here, we identify the major Drosophila α-tubulin acetylase (dTAT) and show that it plays key roles in several forms of mechanosensation. dTAT is highly expressed in the larval peripheral nervous system (PNS), but it is largely dispensable for neuronal morphogenesis. Mutation of the acetylase gene or the K40 acetylation site in α-tubulin impairs mechanical sensitivity in sensory neurons and behavioral responses to gentle touch, harsh touch, gravity, and vibration stimuli, but not noxious thermal stimulus. Finally, we show that dTAT is required for mechanically induced activation of NOMPC, a microtubule-associated transient receptor potential channel, and functions to maintain integrity of the microtubule cytoskeleton in response to mechanical stimulation.

Indexed as

Mechanotransduction, CellularAcetylationAcetyltransferasesAnimalsCells, CulturedDendritesDrosophila melanogasterDrosophila ProteinsLarvaMicrotubulesMorphogenesisPeripheral Nervous SystemTransient Receptor Potential ChannelsAcetyltransferasesalpha-tubulin acetylaseDrosophila ProteinsNOMPC protein, DrosophilaTransient Receptor Potential ChannelsDrosophilamechanosensationmicrotubule acetylationsomatosensory neuronTRP channel

Identifiers

PMID30355484
PMCPMC6248335
OpenAlexW2791455737

What OpenQuestion holds

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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.