Evidence map›Paper›PMID 31002474›Full record

ArticleDevelopmental neurobiology2019

Tao Negatively Regulates BMP Signaling During Neuromuscular Junction Development in Drosophila.

Stephen F Politano, Ryan R Salemme, James Ashley, Javier A López-Rivera, Toren A Bakula, Kathryn A Puhalla, John P Quinn, Madison J Juszczak, Lauren K Phillip, Robert A Carrillo and 1 more

Open access · greenAbstract read
In one paragraph

Article in Developmental neurobiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 35% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Dysregulation of BMP, Wnt, and Insulin Signaling in Fragile X Syndrome.Frontiers in cell and developmental biology · 2022
    Review
  3. Article
  4. 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

11 authors at 2 institutions in 1 country.

Stephen F PolitanoDepartment of Biology, John Carroll University, University Heights, Ohio, 44118.
Ryan R SalemmeDepartment of Biology, John Carroll University, University Heights, Ohio, 44118.
James AshleyMolecular Genetics and Cell Biology, University of Chicago, Chicago, Illinois, 60637.ORCID 0000-0002-6693-1014
Javier A López-RiveraDepartment of Biology, John Carroll University, University Heights, Ohio, 44118.
Toren A BakulaDepartment of Biology, John Carroll University, University Heights, Ohio, 44118.
Kathryn A PuhallaDepartment of Biology, John Carroll University, University Heights, Ohio, 44118.
John P QuinnDepartment of Biology, John Carroll University, University Heights, Ohio, 44118.
Madison J JuszczakDepartment of Biology, John Carroll University, University Heights, Ohio, 44118.
Lauren K PhillipDepartment of Biology, John Carroll University, University Heights, Ohio, 44118.
Robert A CarrilloMolecular Genetics and Cell Biology, University of Chicago, Chicago, Illinois, 60637.ORCID 0000-0002-2067-9861
Pamela J VanderzalmDepartment of Biology, John Carroll University, University Heights, Ohio, 44118.ORCID 0000-0001-9738-7843
John Carroll University · USUniversity of Chicago · US

Funding

Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Cale Whitworth · 2014 to 2026
$13.5M
Drosophila Transgenic RNAi Resource ProjectR01GM084947 · NIGMS · HARVARD MEDICAL SCHOOL · PI PERRIMON, NORBERT · 2008 to 2019
$9.8M
Interactions Between IgSF Proteins in Neural Circuit FormationK01NS102342 · NINDS · UNIVERSITY OF CHICAGO · PI CARRILLO, ROBERT ARNULFO · 2017 to 2019
$684k
NIGMS NIH HHS R01 GM084947NIH HHS P40 OD018537NINDS NIH HHS K01 NS102342ODCDC CDC HHS P40 OD018537
6 · The paper itself

Abstract

The coordinated growth and development of synapses is critical for all aspects of neural circuit function and mutations that disrupt these processes can result in various neurological defects. Several anterograde and retrograde signaling pathways, including the canonical Bone Morphogenic Protein (BMP) pathway, regulate synaptic development in vertebrates and invertebrates. At the Drosophila larval neuromuscular junction (NMJ), the retrograde BMP pathway is a part of the machinery that controls NMJ expansion concurrent with larval growth. We sought to determine whether the conserved Hippo pathway, critical for proportional growth in other tissues, also functions in NMJ development. We found that neuronal loss of the serine-threonine protein kinase Tao, a regulator of the Hippo signaling pathway, results in supernumerary boutons which contain a normal density of active zones. Tao is also required for proper synaptic function, as reduction of Tao results in NMJs with decreased evoked excitatory junctional potentials. Surprisingly, Tao function in NMJ growth is independent of the Hippo pathway. Instead, our experiments suggest that Tao negatively regulates BMP signaling as reduction of Tao leads to an increase in pMad levels in motor neuron nuclei and an increase in BMP target gene expression. Taken together, these results support a role for Tao as a novel inhibitor of BMP signaling in motor neurons during synaptic development and function.

Indexed as

AnimalsAnimals, Genetically ModifiedBone Morphogenetic ProteinsDrosophila melanogasterDrosophila ProteinsNeuromuscular JunctionNeuronal OutgrowthPresynaptic TerminalsProtein Serine-Threonine KinasesSignal TransductionSynaptic TransmissionBone Morphogenetic ProteinsDrosophila ProteinsProtein Serine-Threonine KinasesTao protein, DrosophilaBMP signalingHippo signalingNMJ developmentTao

Identifiers

PMID31002474
PMCPMC6848449
OpenAlexW2935931891

What OpenQuestion holds

Textmetadata
LicenceTDM
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.