Evidence map›Paper›PMID 20352049›Full record

ArticlePloS one2010

Differential expression of the circadian clock in maternal and embryonic tissues of mice.

Hamid Dolatshad, Andrew J Cary, Fred C Davis

Abstract read
In one paragraph

Article in PloS one, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
–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.

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

35 citing papers in PubMed.

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  18. Involvement of posttranscriptional regulation ofProceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  19. Review
  20. The circadian coordination of cell biology.The Journal of cell biology · 2016
    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

3 authors.

Hamid DolatshadDepartment of Biology, Northeastern University, Boston, Massachusetts, United States of America.
Andrew J Cary
Fred C Davis

Funding

SCN Output SignalsR01MH068796 · NIMH · NORTHEASTERN UNIVERSITY · PI DAVIS, FREDERICK C. · 2004 to 2007
$1.1M
NIMH NIH HHS 1 R01 MH068796NIMH NIH HHS R01 MH068796
6 · The paper itself

Abstract

backgroundMolecular feedback loops involving transcription and translation and several key genes are at the core of circadian regulatory cycles affecting cellular pathways and metabolism. These cycles are active in most adult animal cells but little is known about their expression or influence during development. METHODOLOGY/PRINCIPAL

findingsTo determine if circadian cycles are active during mammalian development we measured the expression of key circadian genes during embryogenesis in mice using quantitative real-time RT-PCR. All of the genes examined were expressed in whole embryos beginning at the earliest age examined, embryonic day 10. In contrast to adult tissues, circadian variation was absent for all genes at all of the embryonic ages examined in either whole embryos or individual tissues. Using a bioluminescent fusion protein that tracks translation of the circadian gene, per2, we also analyzed protein levels. Similar to mRNA, a protein rhythm was observed in adult tissue but not in embryonic tissues collected in-vivo. In contrast, when tissues were placed in culture for the continuous assay of bioluminescence, rhythms were observed in embryonic (E18) tissues. We found that placing embryonic tissues in culture set the timing (phase) of these rhythms, suggesting the importance of a synchronizing signal for the expression of circadian cycles in developing tissues. CONCLUSIONS/SIGNIFICANCE: These results show that embryonic tissues express key circadian genes and have the capacity to express active circadian regulatory cycles. In vivo, circadian cycles are not expressed in embryonic tissues as they are in adult tissues. Individual cells might express oscillations, but are not synchronized until later in development.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsCircadian RhythmDevelopmental BiologyFemaleKidneyLiverMaleMiceMice, Inbred C57BLMyocardiumOscillometryReverse Transcriptase Polymerase Chain ReactionTime FactorsTissue Distribution

Identifiers

PMID20352049
PMCPMC2844431

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LicenceCC BY
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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.