Evidence map›Paper›PMID 32460660›Full record

ArticleJournal of biological rhythms2020

Reduced VIP Expression Affects Circadian Clock Function in VIP-IRES-CRE Mice (JAX 010908).

Deborah A M Joye, Kayla E Rohr, Danielle Keller, Thomas Inda, Adam Telega, Harshida Pancholi, Vania Carmona-Alcocer, Jennifer A Evans

Open access · greenAbstract read
In one paragraph

Article in Journal of biological rhythms, 2020. 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
1.5field-weighted citation impact, top 21% 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

17 citing papers in PubMed, 24 citations in OpenAlex.

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  8. GABAergic/Glycinergic and Glutamatergic Neurons Mediate Distinct Neurodevelopmental Phenotypes ofThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
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  11. SIK3-HDAC4 in the suprachiasmatic nucleus regulates the timing of arousal at the dark onset and circadian period in mice.Proceedings of the National Academy of Sciences of the United States of America · 2023
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  14. Cell-Type-Specific Circadian Bioluminescence Rhythms inJournal of biological rhythms · 2022
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  15. Review
  16. Female fertility does not requireFrontiers in endocrinology · 2022
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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

8 authors at 1 institution in 1 country.

Deborah A M JoyeDepartment of Biomedical Sciences, Marquette University, Milwaukee, Wisconsin.
Kayla E RohrDepartment of Biomedical Sciences, Marquette University, Milwaukee, Wisconsin.
Danielle KellerDepartment of Biomedical Sciences, Marquette University, Milwaukee, Wisconsin.
Thomas IndaDepartment of Biomedical Sciences, Marquette University, Milwaukee, Wisconsin.
Adam TelegaDepartment of Biomedical Sciences, Marquette University, Milwaukee, Wisconsin.
Harshida PancholiDepartment of Biomedical Sciences, Marquette University, Milwaukee, Wisconsin.
Vania Carmona-AlcocerDepartment of Biomedical Sciences, Marquette University, Milwaukee, Wisconsin.
Jennifer A EvansDepartment of Biomedical Sciences, Marquette University, Milwaukee, Wisconsin.ORCID 0000-0002-6220-0273
Marquette University · US

Funding

Inhibitory feedback mechanisms that couple circadian clock neurons in mammalsR01NS091234 · NINDS · MARQUETTE UNIVERSITY · PI EVANS, JENNIFER ANNE · 2015 to 2019
$1.7M
NINDS NIH HHS R01 NS091234
6 · The paper itself

Abstract

Circadian rhythms are programmed by the suprachiasmatic nucleus (SCN), which relies on neuropeptide signaling to maintain daily timekeeping. Vasoactive intestinal polypeptide (VIP) is critical for SCN function, but the precise role of VIP neurons in SCN circuits is not fully established. To interrogate their contribution to SCN circuits, VIP neurons can be manipulated specifically using the DNA-editing enzyme Cre recombinase. Although the Cre transgene is assumed to be inert by itself, we find that VIP expression is reduced in both heterozygous and homozygous adult VIP-IRES-Cre mice (JAX 010908). Compared with wild-type mice, homozygous VIP-Cre mice display faster reentrainment and shorter free-running period but do not become arrhythmic in constant darkness. Consistent with this phenotype, homozygous VIP-Cre mice display intact SCN PER2::LUC rhythms, albeit with altered period and network organization. We present evidence that the ability to sustain molecular rhythms in the VIP-Cre SCN is not due to residual VIP signaling; rather, arginine vasopressin signaling helps to sustain SCN function at both intracellular and intercellular levels in this model. This work establishes that the VIP-IRES-Cre transgene interferes with VIP expression but that loss of VIP can be mitigated by other neuropeptide signals to help sustain SCN function. Our findings have implications for studies employing this transgenic model and provide novel insight into neuropeptide signals that sustain daily timekeeping in the master clock.

Indexed as

Circadian ClocksAnimalsCircadian RhythmFemaleIntegrasesMaleMiceNeuronsNeuropeptidesPeriod Circadian ProteinsSignal TransductionSuprachiasmatic NucleusVasoactive Intestinal PeptideCre recombinaseIntegrasesNeuropeptidesPeriod Circadian ProteinsVasoactive Intestinal Peptidearginine vasopressincircadiancre transgeneneuropeptidessuprachiasmatic nucleusvasoactive intestinal polypeptideVIP-IRES-CRE mice (JAX 010908)

Identifiers

PMID32460660
PMCPMC9235543
OpenAlexW3029222739

What OpenQuestion holds

Textmetadata
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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.