Evidence map›Paper›PMID 19289463›Full record

ArticleThe Journal of biological chemistry2009

14-3-3zeta contributes to tyrosine hydroxylase activity in MN9D cells: localization of dopamine regulatory proteins to mitochondria.

Jian Wang, Haiyan Lou, Courtney J Pedersen, Amanda D Smith, Ruth G Perez

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

51 citing papers in PubMed, 78 citations in OpenAlex.

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  10. "Janus-Faced" α-Synuclein: Role in Parkinson's Disease.Frontiers in cell and developmental biology · 2021
    Review
  11. Article
  12. NT5DC2 affects the phosphorylation of tyrosine hydroxylase regulating its catalytic activity.Journal of neural transmission (Vienna, Austria : 1996) · 2020
    Article
  13. Review
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  19. An energetic view of stress: Focus on mitochondria.Frontiers in neuroendocrinology · 2018
    Review
  20. 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

5 authors at 2 institutions in 2 countries.

Jian WangDepartments of Neurology and Pharmacology & Chemical Biology.
Haiyan Lou
Courtney J Pedersen
Amanda D Smith
Ruth G Perez
University of Pittsburgh · USInstitute for Neurodegenerative Disorders · US

Funding

a-Synuclein and Dopamine: Implications of ParkinsonismR01NS042094 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI PEREZ, RUTH G · 2002 to 2010
$2.0M
Cell-based assays for neuroprotection in parkinsonismR21NS045336 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI PEREZ, RUTH G · 2003 to 2004
$283k
NINDS NIH HHS NS42094NINDS NIH HHS R01 NS042094NINDS NIH HHS R21 NS045336
6 · The paper itself

Abstract

The 14-3-3 proteins stimulate the activation of tyrosine hydroxylase (TH), the rate-limiting catecholamine biosynthetic enzyme. To explore if particular endogenous 14-3-3 isoforms specifically affected TH activity and dopamine synthesis, we utilized rodent nigrostriatal tissues and midbrain-derived MN9D dopaminergic cells. Extracts from ventral midbrain and MN9D cells contained similar pools of 14-3-3 mRNAs, with 14-3-3zeta being relatively abundant in both. Protein levels of 14-3-3zeta were also abundant. [(32)P]Orthophosphate labeling of MN9D cells, followed by co-immunoprecipitation with pan-TH and pan-14-3-3 antibodies brought down similar amounts of phosphorylated TH in each, confirming that 14-3-3-bound phosphorylated TH in our cells. Co-immunoprecipitation of striatal tissues with a pan-TH antibody precipitated 14-3-3zeta but not another potential TH regulatory isoform, 14-3-3eta. In whole cell extracts from MN9D cells after 14-3-3 small interfering RNA treatments, we found that 14-3-3zeta knockdown significantly reduced TH activity and dopamine synthesis whereas knockdown of 14-3-3eta had no effect. 14-3-3zeta was found co-localized on mitochondria with TH, and its knockdown by small interfering RNA reduced TH phosphorylation and TH activity in the mitochondrial pool. Together the data support a role for 14-3-3zeta as an endogenous activator of TH in midbrain dopaminergic neurons and furthermore, identify mitochondria as a potential novel site for dopamine synthesis, with implications for Parkinson disease.

Indexed as

14-3-3 ProteinsAnimalsCell LineDihydroxyphenylalanineDopamineGene Expression RegulationImmunoprecipitationMesencephalonMiceMitochondriaNeuronsPhosphorylationProtein IsoformsProtein TransportRatsRNA, Messenger14-3-3 ProteinsDihydroxyphenylalanineDopamineProtein IsoformsRNA, MessengerRNA, Small InterferingTyrosine 3-Monooxygenase

Identifiers

PMID19289463
PMCPMC2682849
OpenAlexW1981605166

What OpenQuestion holds

Textmetadata
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.