Evidence map›Paper›PMID 30279480›Full record

ArticleScientific reports2018

Arc/Arg3.1 has an activity-regulated interaction with PICK1 that results in altered spatial dynamics.

Brandee M S S Goo, Bethany J Sanstrum, Diana Z Y Holden, Yi Yu, Nicholas G James

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. Nanoscale Spatial Organization of ARC High- and Low-Order Assemblies at Excitatory Synapses.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Arc ubiquitination regulates endoplasmic reticulum-mediated CaFrontiers in cellular neuroscience · 2023
    Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Palmitoylated Proteins in Dendritic Spine Remodeling.Frontiers in synaptic neuroscience · 2020
    Article
  14. 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

5 authors at 1 institution in 1 country.

Brandee M S S GooDepartment of Cell and Molecular Biology, John A. Burns School of Medicine, 651 Ilalo St., BSB 222, University of Hawaii, Honolulu, HI, 96813, USA.
Bethany J SanstrumDepartment of Cell and Molecular Biology, John A. Burns School of Medicine, 651 Ilalo St., BSB 222, University of Hawaii, Honolulu, HI, 96813, USA.
Diana Z Y HoldenDepartment of Cell and Molecular Biology, John A. Burns School of Medicine, 651 Ilalo St., BSB 222, University of Hawaii, Honolulu, HI, 96813, USA.
Yi Yu
Nicholas G JamesDepartment of Cell and Molecular Biology, John A. Burns School of Medicine, 651 Ilalo St., BSB 222, University of Hawaii, Honolulu, HI, 96813, USA. njames4@hawaii.edu.
University of Hawaiʻi at Mānoa · US

Funding

TRPA1 Physiology in Diabetes, Metabolic Syndrome, and MetabolismP20GM113134 · NIGMS · UNIVERSITY OF HAWAII AT MANOA · PI Michael A. Ortega · 2017 to 2026
$21.5M
Chromatin Expulsion by the DNA Replication Licensing Factor ORC4 during Asymmetric Cell Division in Meiosis and DifferentiationR01GM123048 · NIGMS · UNIVERSITY OF HAWAII AT MANOA · PI WARD, WILLIAM S · 2018 to 2021
$1.3M
NIGMS NIH HHS P20 GM113134NIGMS NIH HHS R01 GM123048U.S. Department of Health & Human Services | National Institutes of Health (NIH) 1R01GM123048
6 · The paper itself

Abstract

Activity-regulated cytoskeleton-associated protein (Arc; also known as Arg3.1) is an immediate early gene product that is transcribed in dendritic spines and, to date, has been best characterized as a positive regulator of AMPAR endocytosis during long-term depression (LTD) through interaction with endocytic proteins. Here, we show that protein interacting with C terminal kinase 1 (PICK1), a protein known to bind to the GluA2 subunit of AMPARs and associated with AMPAR trafficking, was pulled-down from brain homogenates and synaptosomes when using Arc as immobilized bait. Fluctuation and FLIM-FRET-Phasor analysis revealed direct interaction between these proteins when co-expressed that was increased under depolarizing conditions in live cells. At the plasma membrane, Arc-mCherry oligomerization was found to be concentration dependent. Additionally, co-expression of Arc-mCherry and EGFP-PICK1 followed by depolarizing conditions resulted in significant increases in the number and size of puncta containing both proteins. Furthermore, we identified the Arc binding region to be the first 126 amino acids of the PICK1 BAR domain. Overall, our data support a novel interaction and model where PICK1 mediates Arc regulation of AMPARs particularly under depolarizing conditions.

Indexed as

Protein Interaction MappingAnimalsBrain ChemistryCell Cycle ProteinsCytoskeletal ProteinsDendritic CellsMiceNerve Tissue ProteinsProtein BindingProtein TransportReceptors, Glutamateactivity regulated cytoskeletal-associated proteinCell Cycle ProteinsCytoskeletal ProteinsNerve Tissue ProteinsPrkcabp protein, mouseReceptors, Glutamate

Identifiers

PMID30279480
PMCPMC6168463
OpenAlexW2893074578

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.