Evidence map›Paper›PMID 32354999›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

Mutation of a PER2 phosphodegron perturbs the circadian phosphoswitch.

Shusaku Masuda, Rajesh Narasimamurthy, Hikari Yoshitane, Jae Kyoung Kim, Yoshitaka Fukada, David M Virshup

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 4% 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

49 citing papers in PubMed, 1 synthesis or guideline pooled it, 77 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Oligomerization of PER2 as a dynamic mode of regulation of the mammalian circadian clock.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  7. Review
  8. Review
  9. Post-Translational Modifications in Animal Circadian Clocks.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  10. Article
  11. Review
  12. Review
  13. PERspectives on circadian cell biology.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. Phosphorylation of DNA-binding domains of CLOCK-BMAL1 complex for PER-dependent inhibition in circadian clock of mammalian cells.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  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

6 authors at 4 institutions in 4 countries.

Shusaku MasudaDepartment of Biological Sciences, School of Science, The University of Tokyo, 113-0033 Bunkyo-ku, Tokyo, Japan.ORCID 0000-0003-1701-6685
Rajesh NarasimamurthyProgramme in Cancer and Stem Cell Biology, Duke-NUS Medical School, 169857 Singapore.ORCID 0000-0003-4224-3791
Hikari YoshitaneDepartment of Biological Sciences, School of Science, The University of Tokyo, 113-0033 Bunkyo-ku, Tokyo, Japan.ORCID 0000-0001-6319-3354
Jae Kyoung KimDepartment of Mathematical Sciences, Korea Advanced Institute of Science and Technology, 34141 Daejeon, Korea.ORCID 0000-0001-7842-2172
Yoshitaka FukadaDepartment of Biological Sciences, School of Science, The University of Tokyo, 113-0033 Bunkyo-ku, Tokyo, Japan; sfukada@mail.ecc.u-tokyo.ac.jp David.Virshup@duke-nus.edu.sg.
David M VirshupProgramme in Cancer and Stem Cell Biology, Duke-NUS Medical School, 169857 Singapore; sfukada@mail.ecc.u-tokyo.ac.jp David.Virshup@duke-nus.edu.sg.ORCID 0000-0001-6976-850X
The University of Tokyo · JPDuke Medical Center · USDuke-NUS Medical School · SGKorea Advanced Institute of Science and Technology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Casein kinase 1 (CK1) plays a central role in regulating the period of the circadian clock. In mammals, PER2 protein abundance is regulated by CK1-mediated phosphorylation and proteasomal degradation. On the other hand, recent studies have questioned whether the degradation of the core circadian machinery is a critical step in clock regulation. Prior cell-based studies found that CK1 phosphorylation of PER2 at Ser478 recruits the ubiquitin E3 ligase β-TrCP, leading to PER2 degradation. Creation of this phosphodegron is regulated by a phosphoswitch that is also implicated in temperature compensation. However, in vivo evidence that this phosphodegron influences circadian period is lacking. Here, we generated and analyzed PER2-Ser478Ala knock-in mice. The mice showed longer circadian period in behavioral analysis. Molecularly, mutant PER2 protein accumulated in both the nucleus and cytoplasm of the mouse liver, while

Indexed as

MutationAnimalsBehavior, Animalbeta-Transducin Repeat-Containing ProteinsCasein Kinase ICell NucleusCircadian ClocksCircadian RhythmFemaleGene Expression RegulationLiverMaleMiceMice, Inbred C57BLMice, KnockoutModels, Animalbeta-Transducin Repeat-Containing ProteinsCasein Kinase IPer2 protein, mousePeriod Circadian ProteinsRNA, MessengerUbiquitin-Protein Ligasescircadian clockknock-in mousePeriod2phosphorylationtemperature compensation

Identifiers

PMID32354999
PMCPMC7245125
OpenAlexW3022723204

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.