Evidence map›Paper›PMID 33647263›Full record

ReviewBiochemical pharmacology2021

The role of clock genes in sleep, stress and memory.

Youri G Bolsius, Matias D Zurbriggen, Jae Kyoung Kim, Martien J Kas, Peter Meerlo, Sara J Aton, Robbert Havekes

Open access · hybridAbstract readReview
In one paragraph

Review in Biochemical pharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
4.5field-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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 70 citations in OpenAlex.

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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

7 authors at 4 institutions in 4 countries.

Youri G BolsiusNeurobiology Expertise Group, Groningen Institute for Evolutionary Life Sciences (GELIFES), University of Groningen, Groningen, the Netherlands.
Matias D ZurbriggenInstitute of Synthetic Biology and CEPLAS, University of Düsseldorf, Düsseldorf, Germany.
Jae Kyoung KimDepartment of Mathematical Sciences, Korea Advanced Institute of Science and Technology, Daejeon, Republic of Korea.
Martien J KasNeurobiology Expertise Group, Groningen Institute for Evolutionary Life Sciences (GELIFES), University of Groningen, Groningen, the Netherlands.
Peter MeerloNeurobiology Expertise Group, Groningen Institute for Evolutionary Life Sciences (GELIFES), University of Groningen, Groningen, the Netherlands.
Sara J AtonMolecular, Cellular and Developmental Biology, University of Michigan, Ann Arbor, USA. Electronic address: saton@umich.edu.
Robbert HavekesNeurobiology Expertise Group, Groningen Institute for Evolutionary Life Sciences (GELIFES), University of Groningen, Groningen, the Netherlands. Electronic address: r.havekes@rug.nl.
University of Groningen · NLCluster of Excellence on Plant Sciences · DEKorea Advanced Institute of Science and Technology · KRUniversity of Michigan · US

Funding

Linking network activity and intracellular plasticity mechanisms during sleep-depDP2MH104119 · NIMH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ATON, SARA J · 2013 to 2013
$2.3M
Thalamocortical and corticocortical mechanisms for sleep-dependent visual learningR01NS104776 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ATON, SARA J · 2018 to 2022
$1.9M
Linking interneuron-mediated circuit regulation with sleep-dependent plasticity and memory storage in the hippocampusRF1NS118440 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ATON, SARA J · 2020 to 2020
$1.4M
Linking interneuron-mediated circuit regulation with sleep-dependent plasticity and memory storage in the hippocampusR01NS118440 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ATON, SARA J · 2023 to 2024
$880k
NIMH NIH HHS DP2 MH104119NINDS NIH HHS R01 NS104776NINDS NIH HHS R01 NS118440NINDS NIH HHS RF1 NS118440
6 · The paper itself

Abstract

Circadian clock genes serve as the molecular basis for animals' ~24-h internal timekeeping. Clock gene expression inside and outside of the mammalian brain's circadian pacemaker (i.e. the SCN) integrates temporal information into a wealth of physiological processes. Ample data suggests that in addition to canonical cellular timekeeping functions, clock proteins also interact with proteins involved in cellular processes not related to timekeeping, including protein regulation and the interaction with other signaling mechanisms not directly linked to the regulation of circadian rhythms. Indeed, recent data suggests that clock genes outside the SCN are involved in fundamental brain processes such as sleep/wakefulness, stress and memory. The role of clock genes in these brain processes are complex and divers, influencing many molecular pathways and phenotypes. In this review, we will discuss recent work on the involvement of clock genes in sleep, stress, and memory. Moreover, we raise the controversial possibility that these functions may be under certain circumstances independent of their circadian timekeeping function.

Indexed as

AnimalsCircadian ClocksCircadian RhythmCLOCK ProteinsHumansMemorySleepSleep DeprivationStress, PsychologicalCLOCK protein, humanCLOCK ProteinsBmal1Circadian rhythmClockClock genesCryptochrome1/2GlucocorticoidsLearningMemoryPeriod1/2SleepSleep deprivationSleep lossStressSynaptic plasticity

Identifiers

PMID33647263
PMCPMC9487905
OpenAlexW3134323687

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.