Evidence map›Paper›PMID 34006534›Full record

ArticleLife science alliance2021

Non-microtubule tubulin-based backbone and subordinate components of postsynaptic density lattices.

Tatsuo Suzuki, Nobuo Terada, Shigeki Higashiyama, Kiyokazu Kametani, Yoshinori Shirai, Mamoru Honda, Tsutomu Kai, Weidong Li, Katsuhiko Tabuchi

Open access · goldAbstract read
In one paragraph

Article in Life science alliance, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.1field-weighted citation impact, top 62% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
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 4 institutions in 2 countries.

Tatsuo SuzukiDepartment of Molecular and Cellular Physiology, Shinshu University Academic Assembly, Institute of Medicine, Shinshu University Academic Assembly, Matsumoto, Japan suzukit@shinshu-u.ac.jp.ORCID 0000-0002-3537-5940
Nobuo TeradaHealth Science Division, Department of Medical Sciences, Graduate School of Medicine, Science and Technology, Shinshu University, Matsumoto, Nagano, Japan.
Shigeki HigashiyamaDepartment of Cell Growth and Tumor Regulation, Proteo-Science Center, Ehime University, To-on, Ehime, Japan.
Kiyokazu KametaniDepartment of Veterinary Anatomy, Faculty of Veterinary Medicine, Rakuno Gakuen University, Ebetsu, Japan.
Yoshinori ShiraiDepartment of Molecular and Cellular Physiology, Shinshu University Academic Assembly, Institute of Medicine, Shinshu University Academic Assembly, Matsumoto, Japan.ORCID 0000-0002-3263-4986
Mamoru HondaBioscience Group, Center for Precision Medicine Supports, Pharmaceuticals and Life Sciences Division, Shimadzu Techno-Research, INC, Kyoto, Japan.
Tsutomu KaiBioscience Group, Center for Precision Medicine Supports, Pharmaceuticals and Life Sciences Division, Shimadzu Techno-Research, INC, Kyoto, Japan.
Weidong LiBio-X Institutes, Key Laboratory for the Genetics of Development and Neuropsychiatric Disorders (Ministry of Education), Shanghai Key Laboratory of Psychotic Disorders, and Brain Science and Technology Research Center, Shanghai Jiao Tong University, Shanghai, China.
Katsuhiko TabuchiDepartment of Molecular and Cellular Physiology, Shinshu University Academic Assembly, Institute of Medicine, Shinshu University Academic Assembly, Matsumoto, Japan.ORCID 0000-0002-1673-4637
Shinshu University · JPShimadzu (Japan) · JPEhime University · JPRakuno Gakuen University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A purification protocol was developed to identify and analyze the component proteins of a postsynaptic density (PSD) lattice, a core structure of the PSD of excitatory synapses in the central nervous system. "Enriched"- and "lean"-type PSD lattices were purified by synaptic plasma membrane treatment to identify the protein components by comprehensive shotgun mass spectrometry and group them into minimum essential cytoskeleton (MEC) and non-MEC components. Tubulin was found to be a major component of the MEC, with non-microtubule tubulin widely distributed on the purified PSD lattice. The presence of tubulin in and around PSDs was verified by post-embedding immunogold labeling EM of cerebral cortex. Non-MEC proteins included various typical scaffold/adaptor PSD proteins and other class PSD proteins. Thus, this study provides a new PSD lattice model consisting of non-microtubule tubulin-based backbone and various non-MEC proteins. Our findings suggest that tubulin is a key component constructing the backbone and that the associated components are essential for the versatile functions of the PSD.

Indexed as

AnimalsCell MembraneCerebral CortexCytoskeletonFemaleHippocampusMaleMass SpectrometryMembrane ProteinsMicrotubulesNerve Tissue ProteinsPost-Synaptic DensityRatsRats, WistarSynapsesSynaptic MembranesMembrane ProteinsNerve Tissue Proteinspostsynaptic density proteinsTubulin

Identifiers

PMID34006534
PMCPMC8326785
OpenAlexW3162899669

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.