Evidence map›Paper›PMID 23688429›Full record

ArticleBiochemical and biophysical research communications2013

A novel PGC-1α isoform in brain localizes to mitochondria and associates with PINK1 and VDAC.

Joungil Choi, Vera Venkatanaresh Kumar Batchu, Manfred Schubert, Rudolph J Castellani, James W Russell

Abstract read
In one paragraph

Article in Biochemical and biophysical research communications, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Cell-Specific Deletion of PGC-1α from Medium Spiny Neurons Causes Transcriptional Alterations and Age-Related Motor Impairment.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  7. Article
  8. Article
  9. Diabetes and Cognitive Impairment.Current diabetes reports · 2016
    Review
  10. Review
  11. Article
  12. Brain diabetic neurodegeneration segregates with low intrinsic aerobic capacity.Annals of clinical and translational neurology · 2014
    Article
  13. Article
  14. Article
  15. 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 3 institutions in 1 country.

Joungil ChoiDepartment of Neurology, University of Maryland, Baltimore, MD 21201, USA. jochoi@som.umaryland.edu
Vera Venkatanaresh Kumar Batchu
Manfred Schubert
Rudolph J Castellani
James W Russell
University of Maryland, Baltimore · USNational Institute of Neurological Disorders and Stroke · USVeterans Health Administration · US

Funding

Research BaseP30DK072488 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI MITCHELL, BRAXTON D, TAYLOR, SIMEON I. · 2005 to 2019
$17.3M
Gene Delivery To The Nervous SystemZIANS002997 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI SCHUBERT, MANFRED H · 2009 to 2019
$1.9M
SIRT1 Overexpression in Cellular Mitochondrial Metabolism and FunctionR21RR024888 · NCRR · UNIVERSITY OF MARYLAND BALTIMORE · PI RUSSELL, JAMES W · 2008 to 2009
$413k
NCRR NIH HHS R21 RR024888NCRR NIH HHS RR024888NIDDK NIH HHS P30 DK072488
6 · The paper itself

Abstract

Peroxisome proliferator-activated receptor-gamma co-activator 1α (PGC-1α) and PTEN-induced putative kinase 1 (PINK1) are powerful regulators of mitochondrial function. Here, we report that a previously unrecognized, novel 35 kDa PGC-1α isoform localizes to the mitochondrial inner membrane and matrix in brain as determined by protease protection and carbonate extraction assays, as well as by immunoelectron microscopy. Immunoelectron microscopy and import experiments in vitro revealed that 35 kDa PGC-1α colocalizes and interacts with the voltage-dependent anion channel (VDAC), and that its import depends on VDAC. Valinomycin treatment which depolarizes the membrane potential, abolished mitochondrial localization of the 35 kDa PGC-1α. Using blue native-PAGE, co-immunoprecipitation, and immunoelectron microscopy analyses, we found that the 35 kDa PGC-1α binds and colocalizes with PINK1 in brain mitochondria. This is the first report regarding mitochondrial localization of a novel 35 kDa PGC-1α isoform and its association with PINK1, suggesting possible regulatory roles for mitochondrial function in the brain.

Indexed as

AnimalsHippocampusMiceMice, KnockoutMitochondriaPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaProtein IsoformsProtein KinasesPTEN-Induced Putative KinaseTissue DistributionTrans-ActivatorsTranscription FactorsVoltage-Dependent Anion ChannelsPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPpargc1a protein, mouseProtein IsoformsProtein KinasesPTEN-Induced Putative KinaseTrans-ActivatorsTranscription FactorsVoltage-Dependent Anion Channels

Identifiers

PMID23688429
PMCPMC3733220
OpenAlexW1992987001

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.