Evidence map›Paper›PMID 22042857›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2011

Cell-autonomous circadian clock of hepatocytes drives rhythms in transcription and polyamine synthesis.

Ann Atwood, Robert DeConde, Susanna S Wang, Todd C Mockler, Jamal S M Sabir, Trey Ideker, Steve A Kay

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

25 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
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  6. Review
  7. Article
  8. How the Intensity of Night Shift Work Affects Breast Cancer Risk.International journal of environmental research and public health · 2021
    Article
  9. Revealing the hidden reality of the mammalian 12-h ultradian rhythms.Cellular and molecular life sciences : CMLS · 2021
    Review
  10. Translational Regulation of Clock Genes BMAL1 and REV-ERBα by Polyamines.International journal of molecular sciences · 2021
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Circadian mRNA expression: insights from modeling and transcriptomics.Cellular and molecular life sciences : CMLS · 2016
    Review
  17. Article
  18. Review
  19. Article
  20. Article
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

7 authors at 3 institutions in 2 countries.

Ann AtwoodSection of Cell and Developmental Biology, Division of Biological Sciences, and the Center for Chronobiology, University of California at San Diego, La Jolla, CA 92093-0130, USA.
Robert DeConde
Susanna S Wang
Todd C Mockler
Jamal S M Sabir
Trey Ideker
Steve A Kay
University of California, San Diego · USDonald Danforth Plant Science Center · USKing Abdulaziz University · SA

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007198 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHI, NEIL C, INSEL, PAUL A · 1985 to 2024
$29.3M
GENETIC MECHANISMS AND REGULATIONT32GM007240 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HAMPTON, RANDOLPH Y. · 1985 to 2019
$23.8M
SYNTHETIC SYSTEMSP50GM085764 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI WINZELER, ELIZABETH A · 2010 to 2018
$23.3M
MOLECULAR ANALYSIS OF CIRCADIAN RHYTHMS IN SINGLE CELLSR01MH051573 · NIMH · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI KAY, STEVE A · 1994 to 2013
$4.9M
Role of Ror proteins in the mammalian circadian clockR01GM074868 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI KAY, STEVE A · 2006 to 2014
$3.2M
NIGMS NIH HHS GM07240NIGMS NIH HHS P50 GM085764NIGMS NIH HHS P50GM085764NIGMS NIH HHS R01 GM074868NIGMS NIH HHS T32 GM007198NIGMS NIH HHS T32 GM007240NIMH NIH HHS R01 MH051573
6 · The paper itself

Abstract

The circadian clock generates daily rhythms in mammalian liver processes, such as glucose and lipid homeostasis, xenobiotic metabolism, and regeneration. The mechanisms governing these rhythms are not well understood, particularly the distinct contributions of the cell-autonomous clock and central pacemaker to rhythmic liver physiology. Through microarray expression profiling in Met murine hepatocytes (MMH)-D3, we identified over 1,000 transcripts that exhibit circadian oscillations, demonstrating that the cell-autonomous clock can drive many rhythms, and that MMH-D3 is a valid circadian model system. The genes represented by these circadian transcripts displayed both cophasic and antiphasic organization within a protein-protein interaction network, suggesting the existence of competition for binding sites or partners by genes of disparate transcriptional phases. Multiple pathways displayed enrichment in MMH-D3 circadian transcripts, including the polyamine synthesis module of the glutathione metabolic pathway. The polyamine synthesis module, which is highly associated with cell proliferation and whose products are required for initiation of liver regeneration, includes enzymes whose transcripts exhibit circadian oscillations, such as ornithine decarboxylase and spermidine synthase. Metabolic profiling revealed that the enzymatic product of spermidine synthase, spermidine, cycles as well. Thus, the cell-autonomous hepatocyte clock can drive a significant amount of transcriptional rhythms and orchestrate physiologically relevant modules such as polyamine synthesis.

Indexed as

Circadian RhythmTranscription, GeneticAnimalsBiogenic PolyaminesHepatocytesMiceBiogenic Polyamines

Identifiers

PMID22042857
PMCPMC3215069
OpenAlexW2148900913

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.