Evidence map›Paper›PMID 22009745›Full record

ArticleThe Journal of biological chemistry2011

Characterization of novel peroxisome proliferator-activated receptor γ coactivator-1α (PGC-1α) isoform in human liver.

Thomas K Felder, Selma M Soyal, Hannes Oberkofler, Penelope Hahne, Simon Auer, Richard Weiss, Gabriele Gadermaier, Karl Miller, Franz Krempler, Harald Esterbauer and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
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  5. Article
  6. Selective Activation of CNS and ReferenceInternational journal of molecular sciences · 2021
    Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Mitochondrial regulator PGC-1a-Modulating the modulator.Current opinion in endocrine and metabolic research · 2019
    Article
  13. Review
  14. Article
  15. Article
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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

11 authors at 4 institutions in 1 country.

Thomas K FelderDepartment of Laboratory Medicine, Paracelsus Medical University, 5020 Salzburg, Austria.
Selma M Soyal
Hannes Oberkofler
Penelope Hahne
Simon Auer
Richard Weiss
Gabriele Gadermaier
Karl Miller
Franz Krempler
Harald Esterbauer
Wolfgang Patsch
Paracelsus Medical University · ATUniversity of Salzburg · ATBarmherzige Schwestern Krankenhaus Wien · ATMedical University of Vienna · AT

Funding

Austrian Science Fund FWF P 19893
6 · The paper itself

Abstract

Peroxisome proliferator-activated receptor γ coactivator-1α (PGC-1α) is a transcriptional coactivator that contributes to the regulation of numerous transcriptional programs including the hepatic response to fasting. Mechanisms at transcriptional and post-transcriptional levels allow PGC-1α to support distinct biological pathways. Here we describe a novel human liver-specific PGC-1α transcript that results from alternative promoter usage and is induced by FOXO1 as well as glucocorticoids and cAMP-response element-binding protein signaling but is not present in other mammals. Hepatic tissue levels of novel and wild-type transcripts were similar but were only moderately associated (p < 0.003). Novel mRNA levels were associated with a polymorphism located in its promoter region, whereas wild-type transcript levels were not. Furthermore, hepatic PCK1 mRNA levels exhibited stronger associations with the novel than with the wild-type transcript levels. Except for a deletion of 127 amino acids at the N terminus, the protein, termed L-PGC-1α, is identical to PGC-1α. L-PGC-1α was localized in the nucleus and showed coactivation properties that overlap with those of PGC-1α. Collectively, our data support a role of L-PGC-1α in gluconeogenesis, but functional differences predicted from the altered structure suggest that L-PGC-1α may have arisen to adapt PGC-1α to more complex metabolic pathways in humans.

Indexed as

8-Bromo Cyclic Adenosine MonophosphateAnimalsBlotting, NorthernChromatin ImmunoprecipitationDexamethasoneFemaleGene ExpressionGenotypeHeat-Shock ProteinsHep G2 CellsHumansImmunoblottingIn Vitro TechniquesLiverMiceMicroscopy, Fluorescence8-Bromo Cyclic Adenosine MonophosphateDexamethasoneHeat-Shock ProteinsPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPPARGC1A protein, humanProtein IsoformsRNA, MessengerTranscription Factors

Identifiers

PMID22009745
PMCPMC3234813
OpenAlexW2073089207

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.