Evidence map›Paper›PMID 22817841›Full record

ReviewTrends in endocrinology and metabolism: TEM2012

Transcriptional integration of mitochondrial biogenesis.

Richard C Scarpulla, Rick B Vega, Daniel P Kelly

Registry-linked trialAbstract readReview
In one paragraph

Review in Trends in endocrinology and metabolism: TEM, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01911091 (Identification of Novel Skeletal Muscle-derived Factors That Promote Lipid Oxidation in Both Skeletal Muscle and Adipose Tissue), which is not on this map. Cited by 464 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
464citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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.

NCT01911091 naactive not recruitingnot on this mapstarted 2013, after this paper: background citation

Identification of Novel Skeletal Muscle-derived Factors That Promote Lipid Oxidation in Both Skeletal Muscle and Adipose Tissue

TypeinterventionalSponsorAdventHealth Translational Research InstituteRan2013 to 2026Enrolled56ConditionsObesity, Disorder of Lipid Storage and Metabolism, Lipid Metabolism Disorders, Metabolic DisorderArmsExercise
3 · Its place in the literature

Who cites it

464 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Norepinephrine regulates hippocampal mitochondrial biogenesis via β2-adrenergic receptor signaling and PGC-1α.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Hyperlipidemia in membranous nephropathy.Clinical kidney journal · 2026
    Review
  19. Review
  20. Review

404 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

3 authors.

Richard C ScarpullaDepartment of Cell and Molecular Biology, Northwestern University Medical School, Chicago, IL 60611, USA.
Rick B Vega
Daniel P Kelly

Funding

REGULATION OF FATTY ACID OXIDATION DURING CARDIAC GROWTHR01HL058493 · NHLBI · WASHINGTON UNIVERSITY · PI KELLY, DANIEL PATRICK · 1998 to 2024
$10.6M
Molecular Control of Muscle Fuel MetabolismR01DK045416 · NIDDK · WASHINGTON UNIVERSITY · PI KELLY, DANIEL PATRICK · 1996 to 2020
$8.1M
TRANSCRIPTIONAL CONTROL BY NUCLEAR RESPIRATORY FACTORSR01GM032525 · NIGMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SCARPULLA, RICHARD · 1985 to 2012
$4.6M
A Genomic/Metabolomic Strategy to Characterize Cardiac Mitochondrial DysfunctionR01HL101189 · NHLBI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI KELLY, DANIEL PATRICK, MUOIO, DEBORAH M · 2010 to 2013
$2.9M
NHLBI NIH HHS R01 HL058493NHLBI NIH HHS R01 HL101189NIDDK NIH HHS R01 DK045416NIGMS NIH HHS R01 GM032525NIGMS NIH HHS R01 GM32525-28
6 · The paper itself

Abstract

Gene regulatory factors encoded by the nuclear genome are essential for mitochondrial biogenesis and function. Some of these factors act exclusively within the mitochondria to regulate the control of mitochondrial transcription, translation, and other functions. Others govern the expression of nuclear genes required for mitochondrial metabolism and organelle biogenesis. The peroxisome proliferator-activated receptor γ coactivator-1 (PGC-1) family of transcriptional coactivators play a major role in transducing and integrating physiological signals governing metabolism, differentiation, and cell growth to the transcriptional machinery controlling mitochondrial functional capacity. Thus, the PGC-1 coactivators serve as a central component of the transcriptional regulatory circuitry that coordinately controls the energy-generating functions of mitochondria in accordance with the metabolic demands imposed by changing physiological conditions, senescence, and disease.

Indexed as

AnimalsGene Expression RegulationHumansMitochondrial TurnoverPeroxisome Proliferator-Activated ReceptorsTranscription, GeneticPeroxisome Proliferator-Activated Receptors

Identifiers

PMID22817841
PMCPMC3580164

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Registered trials

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.