Evidence map›Paper›PMID 21514156›Full record

ArticleCurrent biology : CB2011

NEMO kinase contributes to core period determination by slowing the pace of the Drosophila circadian oscillator.

Wangjie Yu, Jerry H Houl, Paul E Hardin

Open access · bronzeAbstract read
In one paragraph

Article in Current biology : CB, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

39 citing papers in PubMed, 59 citations in OpenAlex.

  1. Post-Translational Modifications in Animal Circadian Clocks.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  2. Alternative splicing ofProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  3. Alternative splicing ofbioRxiv : the preprint server for biology · 2024
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Decapentaplegic Acutely Defines the Connectivity of Central Pacemaker Neurons inThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  10. Article
  11. Article
  12. Wallenda-Nmo Axis Regulates Growth via Hippo Signaling.Frontiers in cell and developmental biology · 2021
    Article
  13. Review
  14. Review
  15. AMP-Activated Protein Kinase Regulates Circadian Rhythm by Affecting CLOCK inThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  16. CK1α Collaborates with DOUBLETIME to Regulate PERIOD Function in theThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  17. Article
  18. Review
  19. Review
  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

3 authors at 1 institution in 1 country.

Wangjie YuDepartment of Biology and The Center for Biological Clocks Research, Texas A&M University, College Station, TX 77845-3258, USA.
Jerry H Houl
Paul E Hardin
Texas A&M University · US

Funding

Regulation of Circadian TranscriptionR01NS052854 · NINDS · TEXAS A&M UNIVERSITY · PI HARDIN, PAUL E · 2006 to 2014
$2.7M
NINDS NIH HHS NS052854NINDS NIH HHS R01 NS052854
6 · The paper itself

Abstract

The Drosophila circadian oscillator is comprised of transcriptional feedback loops that are activated by CLOCK (CLK) and CYCLE (CYC) and repressed by PERIOD (PER) and TIMELESS (TIM) [1]. The timing of CLK-CYC activation and PER-TIM repression is regulated posttranslationally, in part through rhythmic phosphorylation of CLK, PER, and TIM [2-4]. Although kinases that control PER and TIM levels and subcellular localization have been identified [5-10], additional kinases are predicted to target PER, TIM, and/or CLK to promote time-specific transcriptional repression. We screened for kinases that alter circadian behavior via clock cell-directed RNA interference (RNAi) and identified the proline-directed kinase nemo (nmo) as a novel component of the circadian oscillator. Both nmo RNAi knockdown and a nmo hypomorphic mutant shorten circadian period, whereas nmo overexpression lengthens circadian period. CLK levels increase when nmo expression is knocked down in clock cells, whereas CLK levels decrease and PER and TIM accumulation are delayed when nmo is overexpressed in clock cells. These data suggest that nmo slows the pace of the circadian oscillator by altering CLK, PER, and TIM expression, thereby contributing to the generation of an ~24 hr circadian period.

Indexed as

AnimalsARNTL Transcription FactorsBiological ClocksCircadian RhythmCLOCK ProteinsDrosophilaDrosophila ProteinsGene Expression RegulationMitogen-Activated Protein KinasesPeriod Circadian ProteinsPhosphorylationRNA InterferenceARNTL Transcription FactorsClk protein, DrosophilaCLOCK Proteinscyc protein, DrosophilaDrosophila ProteinsMitogen-Activated Protein Kinasesnmo protein, DrosophilaPeriod Circadian ProteinsPER protein, Drosophilatim protein, Drosophila

Identifiers

PMID21514156
PMCPMC3090582
OpenAlexW2052531367

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.