Evidence map›Paper›PMID 22722938›Full record

ArticleThe Journal of biological chemistry2012

Dopamine transporter phosphorylation site threonine 53 regulates substrate reuptake and amphetamine-stimulated efflux.

James D Foster, Jae-Won Yang, Amy E Moritz, Sathyavathi Challasivakanaka, Margaret A Smith, Marion Holy, Kyle Wilebski, Harald H Sitte, Roxanne A Vaughan

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

65 citing papers in PubMed, 94 citations in OpenAlex.

  1. Article
  2. Article
  3. Hypocretin receptor 1 blockade early in abstinence prevents incubation of cocaine seeking and normalizes dopamine transmission.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  4. Transient Suppression of Dopamine Transporter Palmitoylation by Methamphetamine: Implications for Transport Regulation.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
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  19. Article
  20. Substance abuse and neurotransmission.Advances in pharmacology (San Diego, Calif.) · 2022
    Article

5 more citing papers are in PubMed but not listed here.

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 2 institutions in 2 countries.

James D FosterDepartment of Biochemistry and Molecular Biology, University of North Dakota School of Medicine and Health Sciences, Grand Forks, ND 58202-9037, USA.
Jae-Won Yang
Amy E Moritz
Sathyavathi Challasivakanaka
Margaret A Smith
Marion Holy
Kyle Wilebski
Harald H Sitte
Roxanne A Vaughan
University of North Dakota · USMedical University of Vienna · AT

Funding

WORKSHOPS AND EVALUATIONP20RR016471 · NCRR · UNIVERSITY OF NORTH DAKOTA · PI KELLER, CHRISTOPHER P · 2001 to 2011
$31.7M
TRPC1, CALCIUM AND PARKINSON'S DISEASEP20RR017699 · NCRR · UNIVERSITY OF NORTH DAKOTA · PI GHRIBI, OTHMAN · 2002 to 2011
$19.7M
Phosphorylation and Regulation of Dopamine TransportersR01DA013147 · NIDA · UNIVERSITY OF NORTH DAKOTA · PI VAUGHAN, ROXANNE A · 1999 to 2010
$2.5M
NCRR NIH HHS P20 RR016471NCRR NIH HHS P20 RR016741NCRR NIH HHS P20 RR017699NIDA NIH HHS R01 DA013147NIDA NIH HHS R01 DA13147
6 · The paper itself

Abstract

In the central nervous system, levels of extraneuronal dopamine are controlled primarily by the action of the dopamine transporter (DAT). Multiple signaling pathways regulate transport activity, substrate efflux, and other DAT functions through currently unknown mechanisms. DAT is phosphorylated by protein kinase C within a serine cluster at the distal end of the cytoplasmic N terminus, whereas recent work in model cells revealed proline-directed phosphorylation of rat DAT at membrane-proximal residue Thr(53). In this report, we use mass spectrometry and a newly developed phospho-specific antibody to positively identify DAT phosphorylation at Thr(53) in rodent striatal tissue and heterologous expression systems. Basal phosphorylation of Thr(53) occurred with a stoichiometry of ~50% and was strongly increased by phorbol esters and protein phosphatase inhibitors, demonstrating modulation of the site by signaling pathways that impact DAT activity. Mutations of Thr(53) to prevent phosphorylation led to reduced dopamine transport V(max) and total apparent loss of amphetamine-stimulated substrate efflux, supporting a major role for this residue in the transport kinetic mechanism.

Indexed as

Amino Acid SubstitutionAmphetamineAnimalsBiological Transport, ActiveCell Line, TumorDopamine AgentsDopamine Plasma Membrane Transport ProteinsMutation, MissensePhosphorylationRatsSignal TransductionSwineThreonineAmphetamineDopamine AgentsDopamine Plasma Membrane Transport ProteinsThreonine

Identifiers

PMID22722938
PMCPMC3436161
OpenAlexW1975102846

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.