Evidence map›Paper›PMID 31258021›Full record

ArticleJournal of biological rhythms2019

Phosphorylation of CRY1 Serine 71 Alters Voluntary Activity but Not Circadian Rhythms In Vivo.

Megan Vaughan, Sabine D Jordan, Drew Duglan, Alanna B Chan, Megan Afetian, Katja A Lamia

Open access · greenAbstract read
In one paragraph

Article in Journal of biological rhythms, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 41% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Vulnerability to helpless behavior is regulated by the circadian clock component CRYPTOCHROME in the mouse nucleus accumbens.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  9. 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

6 authors at 1 institution in 1 country.

Megan VaughanDepartment of Molecular Medicine, Scripps Research, La Jolla, California, USA.ORCID 0000-0002-8289-0638
Sabine D JordanDepartment of Molecular Medicine, Scripps Research, La Jolla, California, USA.
Drew DuglanDepartment of Molecular Medicine, Scripps Research, La Jolla, California, USA.
Alanna B ChanDepartment of Molecular Medicine, Scripps Research, La Jolla, California, USA.ORCID 0000-0003-1239-9349
Megan AfetianDepartment of Molecular Medicine, Scripps Research, La Jolla, California, USA.
Katja A LamiaDepartment of Molecular Medicine, Scripps Research, La Jolla, California, USA.ORCID 0000-0001-9533-0499
Scripps Institution of Oceanography · US

Funding

Circadian molecular regulation of the xenobiotic responseR01DK097164 · NIDDK · SCRIPPS RESEARCH INSTITUTE, THE · PI LAMIA, KATJA A · 2013 to 2017
$2.1M
Regulation of exercise physiology by mammalian cryptochromesR01DK112927 · NIDDK · SCRIPPS RESEARCH INSTITUTE, THE · PI LAMIA, KATJA A · 2018 to 2021
$1.7M
Circadian Repressors Cry1 and Cry2 Modulate Nuclear Hormone Receptor FunctionK01DK090188 · NIDDK · SCRIPPS RESEARCH INSTITUTE, THE · PI LAMIA, KATJA A · 2011 to 2013
$446k
NIDDK NIH HHS K01 DK090188NIDDK NIH HHS R01 DK097164NIDDK NIH HHS R01 DK112927
6 · The paper itself

Abstract

Circadian clocks allow organisms to anticipate repetitive changes in their environment such as food availability, temperature, and predation. While they most clearly manifest at the behavioral level, driving sleep-wake cycles, for example, they also provide critical temporal regulation at the level of individual tissues. Circadian clocks within organs act to ensure that each tissue is functioning in a coordinated manner to anticipate the needs of the organism as a whole but also allow for adaptation of organs to their local environment. One critical aspect of this environment is energy availability, which is communicated at the cellular level via changes in metabolites such as ATP, calcium, and NADH. AMP-activated protein kinase (AMPK) is both sensitive to fluctuations in secondary metabolites and capable of resetting the circadian clock via destabilization of the core clock components CRY and PER. Phosphorylation of serine 71 of CRY1 by AMPK destabilizes CRY1 by decreasing its interaction with binding partner PER2, thus enabling greater association with the SCF complex substrate adaptor FBXL3. Here, we describe a transgenic mouse harboring germline mutation of CRY1 serine 71 to alanine. Unexpectedly, this mutation does not affect the steady-state level of CRY1 protein in mouse livers or quadriceps. We also did not detect changes in either behavioral or molecular circadian rhythms, but female

Indexed as

Behavior, AnimalCircadian RhythmAnimalsCryptochromesFemaleMaleMicePhosphorylationSerineCry1 protein, mouseCryptochromesSerineAMPKcircadianCRY1cryptochromeperiodvoluntary activity

Identifiers

PMID31258021
PMCPMC6813908
OpenAlexW2955179733

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.