Evidence map›Paper›PMID 36977416›Full record

ArticleCurrent biology : CB2023

Behavioral circatidal rhythms require Bmal1 in Parhyale hawaiensis.

Erica R Kwiatkowski, Yisrael Schnytzer, Joshua J C Rosenthal, Patrick Emery

Abstract read
In one paragraph

Article in Current biology : CB, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
  2. Review
  3. Ballistic food approaches inbioRxiv : the preprint server for biology · 2026
    Article
  4. Revitalizing the "biology" in "chronobiology".Npj biological timing and sleep · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Coevolution ofiScience · 2025
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Editorial: Rising stars in chronobiology 2022.Frontiers in physiology · 2024
    Article
  16. Review
  17. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Erica R KwiatkowskiDepartment of Neurobiology, University of Massachusetts Chan Medical School, Worcester, MA 01605, USA.
Yisrael SchnytzerThe Leslie and Susan Gonda Multidisciplinary Brain Research Center, Bar-Ilan University, Ramat Gan 5290002, Israel; The Eugene Bell Center, The Marine Biological Laboratory, Woods Hole, MA 02543, USA.
Joshua J C RosenthalThe Eugene Bell Center, The Marine Biological Laboratory, Woods Hole, MA 02543, USA.
Patrick EmeryDepartment of Neurobiology, University of Massachusetts Chan Medical School, Worcester, MA 01605, USA. Electronic address: patrick.emery@umassmed.edu.

Funding

Molecular and neural mechanisms generating and synchronizing circadian rhythmsR35GM118087 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI EMERY, PATRICK · 2016 to 2020
$4.4M
NIGMS NIH HHS R35 GM118087
6 · The paper itself

Abstract

Organisms living in the intertidal zone are exposed to a particularly challenging environment. In addition to daily changes in light intensity and seasonal changes in photoperiod and weather patterns, they experience dramatic oscillations in environmental conditions due to the tides. To anticipate tides, and thus optimize their behavior and physiology, animals occupying intertidal ecological niches have acquired circatidal clocks. Although the existence of these clocks has long been known, their underlying molecular components have proven difficult to identify, in large part because of the lack of an intertidal model organism amenable to genetic manipulation. In particular, the relationship between the circatidal and circadian molecular clocks, and the possibility of shared genetic components, has been a long-standing question. Here, we introduce the genetically tractable crustacean Parhyale hawaiensis as a system for the study of circatidal rhythms. First, we show that P. hawaiensis exhibits robust 12.4-h rhythms of locomotion that can be entrained to an artificial tidal regimen and are temperature compensated. Using CRISPR-Cas9 genome editing, we then demonstrate that the core circadian clock gene Bmal1 is required for circatidal rhythms. Our results thus demonstrate that Bmal1 is a molecular link between circatidal and circadian clocks and establish P. hawaiensis as a powerful system to study the molecular mechanisms underlying circatidal rhythms and their entrainment.

Indexed as

AmphipodaCircadian ClocksAnimalsCircadian RhythmLocomotionPhotoperiodBMAL1circadian rhythmscircatidal rhythmsCRISPR-Cas9 mediated mutagenesisParhyale hawaiensis

Identifiers

PMID36977416
PMCPMC10205697

What Socratic holds

Textmetadata
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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 Socratic graph.