Evidence map›Paper›PMID 19805059›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2009

Glucocorticoid regulation of the circadian clock modulates glucose homeostasis.

Alex Y -L So, Teresita U Bernal, Marlisa L Pillsbury, Keith R Yamamoto, Brian J Feldman

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 215 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
215citing papers in PubMed, 1 pooled it
6.6field-weighted citation impact, top 2% 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

215 citing papers in PubMed, 1 synthesis or guideline pooled it, 437 citations in OpenAlex.

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  12. The sleep-wake history contributes to rhythmic BMAL1 chromatin binding in the cerebral cortex but not in the liver.Proceedings of the National Academy of Sciences of the United States of America · 2025
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155 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

5 authors at 1 institution in 1 country.

Alex Y -L SoDepartment of Pediatrics, University of California, 513 Parnassus Drive, San Francisco, CA 94143, USA.
Teresita U Bernal
Marlisa L Pillsbury
Keith R Yamamoto
Brian J Feldman
University of California, San Francisco · US

Funding

Maximizing Opportunities for Research Excellence - Evaluation Training SupplementR25GM056847 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI DUNCAN, D'ANNE S., SELLO, JASON K · 1998 to 2023
$14.1M
GENE REGULATION BY STEROID RECEPTOR PROTEINSR01CA020535 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI YAMAMOTO, KEITH ROBERT · 1985 to 2018
$8.9M
The Role of Glucocorticoids in Cell Fate DeterminationK08DK073697 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI FELDMAN, BRIAN J · 2006 to 2010
$652k
GENE REGULATION BY STEROID RECEPTOR PROTEINSR37CA020535 · NCI · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI YAMAMOTO, KEITH ROBERT · 1990 to 1998
–
NCI NIH HHS CA 20535NCI NIH HHS R01 CA020535NCI NIH HHS R37 CA020535NIDDK NIH HHS DK 73697NIDDK NIH HHS K08 DK073697NIGMS NIH HHS GM 56847NIGMS NIH HHS R25 GM056847
6 · The paper itself

Abstract

Circadian clock genes are regulated by glucocorticoids; however, whether this regulation is a direct or secondary effect and the physiological consequences of this regulation were unknown. Here, we identified glucocorticoid response elements (GREs) at multiple clock genes and showed that 3 were directly regulated by the glucocorticoid receptor. We determined that a GRE within the core clock gene Per2 was continuously occupied during rhythmic expression and essential for glucocorticoid regulation of that gene in vivo. We further demonstrated that mice with a genomic deletion spanning this GRE expressed elevated leptin levels and were protected from glucose intolerance and insulin resistance on glucocorticoid treatment but not from muscle wasting. We conclude that Per2 is an integral component of a particular glucocorticoid regulatory pathway and that glucocorticoid regulation of the peripheral clock is selectively required for some actions of glucocorticoids.

Indexed as

AnimalsCell Cycle ProteinsCircadian RhythmGene Expression RegulationGlucocorticoidsGlucoseHomeostasisLeptinMesenchymal Stem CellsMiceNuclear ProteinsPeriod Circadian ProteinsPolymerase Chain ReactionTranscription FactorsTranscription, GeneticBhlhb3 protein, mouseCell Cycle ProteinsGlucocorticoidsGlucoseLeptinNuclear ProteinsPer2 protein, mousePeriod Circadian ProteinsTranscription Factors

Identifiers

PMID19805059
PMCPMC2757402
OpenAlexW1998522501

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.