Evidence map›Paper›PMID 33370580›Full record

ReviewCellular signalling2021

Translating around the clock: Multi-level regulation of post-transcriptional processes by the circadian clock.

Amber A Parnell, Aliza K De Nobrega, Lisa C Lyons

Open access · greenAbstract readReview
In one paragraph

Review in Cellular signalling, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

22 citing papers in PubMed, 35 citations in OpenAlex.

  1. Co-expression network analysis reveals repression ofbioRxiv : the preprint server for biology · 2026
    Article
  2. Review
  3. Hydantion indolinones as AANAT inhibitors.Bioorganic & medicinal chemistry letters · 2026
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Impact of Circadian ClockInternational journal of molecular sciences · 2024
    Article
  10. Review
  11. Article
  12. Circadian Regulation of Macrophages and Osteoclasts in Rheumatoid Arthritis.International journal of molecular sciences · 2023
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. 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 at 1 institution in 1 country.

Amber A ParnellDepartment of Biological Science, Program in Neuroscience, Florida State University, Tallahassee, FL 32306, USA.
Aliza K De NobregaDepartment of Biological Science, Program in Neuroscience, Florida State University, Tallahassee, FL 32306, USA.
Lisa C LyonsDepartment of Biological Science, Program in Neuroscience, Florida State University, Tallahassee, FL 32306, USA. Electronic address: lyons@bio.fsu.edu.
Florida State University · US

Funding

Mechanistic Studies on the Impact of Sleep Deprivation on Gene RegulationR01AG062398 · NIA · UNIVERSITY OF IOWA · PI ABEL, EDWIN TED G., LYONS, LISA CARLSON · 2019 to 2023
$3.8M
NIA NIH HHS R01 AG062398
6 · The paper itself

Abstract

The endogenous circadian clock functions to maintain optimal physiological health through the tissue specific coordination of gene expression and synchronization between tissues of metabolic processes throughout the 24 hour day. Individuals face numerous challenges to circadian function on a daily basis resulting in significant incidences of circadian disorders in the United States and worldwide. Dysfunction of the circadian clock has been implicated in numerous diseases including cancer, diabetes, obesity, cardiovascular and hepatic abnormalities, mood disorders and neurodegenerative diseases. The circadian clock regulates molecular, metabolic and physiological processes through rhythmic gene expression via transcriptional and post-transcriptional processes. Mounting evidence indicates that post-transcriptional regulation by the circadian clock plays a crucial role in maintaining tissue specific biological rhythms. Circadian regulation affecting RNA stability and localization through RNA processing, mRNA degradation, and RNA availability for translation can result in rhythmic protein synthesis, even when the mRNA transcripts themselves do not exhibit rhythms in abundance. The circadian clock also targets the initiation and elongation steps of translation through multiple pathways. In this review, the influence of the circadian clock across the levels of post-transcriptional, translation, and post-translational modifications are examined using examples from humans to cyanobacteria demonstrating the phylogenetic conservation of circadian regulation. Lastly, we briefly discuss chronotherapies and pharmacological treatments that target circadian function. Understanding the complexity and levels through which the circadian clock regulates molecular and physiological processes is important for future advancement of therapeutic outcomes.

Indexed as

AnimalsCircadian ClocksCLOCK ProteinsHumansMicroRNAsProtein Processing, Post-TranslationalRibosomesRNA, MessengerRNA Processing, Post-TranscriptionalRNA StabilityCLOCK ProteinsMicroRNAsRNA, MessengerBiological RhythmsCircadian clockPost-transcriptional modificationPost-translational modificationTranslation

Identifiers

PMID33370580
PMCPMC8054296
OpenAlexW3117525363

What OpenQuestion holds

Textmetadata
LicenceTDM
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.