Evidence map›Paper›PMID 39420030›Full record

ArticleScientific reports2024

Identification of shared gene expression programs activated in multiple modes of torpor across vertebrate clades.

Kurt Weir, Natasha Vega, Veronica F Busa, Ben Sajdak, Les Kallestad, Dana Merriman, Krzysztof Palczewski, Joseph Carroll, Seth Blackshaw

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

9 authors.

Kurt WeirDepartment of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Natasha VegaDepartment of Biology, Johns Hopkins University Krieger School of Arts and Sciences, Baltimore, MD, USA.
Veronica F BusaGerman Cancer Research Center (DKFZ), Heidelberg, Germany.
Ben SajdakCell Biology, Neurobiology and Anatomy, Medical College of Wisconsin, Milwaukee, WI, USA.
Les KallestadDepartment of Ophthalmology, Gavin Herbert Eye Institute, University of California Irvine, Irvine, CA, 92697, USA.
Dana MerrimanBiology, University of Wisconsin Oshkosh, Oshkosh, WI, USA.
Krzysztof PalczewskiDepartment of Ophthalmology, Gavin Herbert Eye Institute, University of California Irvine, Irvine, CA, 92697, USA.
Joseph CarrollCell Biology, Neurobiology and Anatomy, Medical College of Wisconsin, Milwaukee, WI, USA.
Seth BlackshawDepartment of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA. sblack@jhmi.edu.

Funding

Use of systems pharmacology to prevent rod and cone photoreceptor degenerationR24EY027283 · NEI · UNIVERSITY OF CALIFORNIA-IRVINE · PI PALCZEWSKI, KRZYSZTOF · 2017 to 2021
$7.9M
Developing Cone-Dominant Retinal Disease Models as a Resource for Translational Vision ResearchU24EY029891 · NEI · MEDICAL COLLEGE OF WISCONSIN · PI CARROLL, JOSEPH, DUNCAN, JACQUE LYNNE · 2018 to 2022
$6.6M
NEI UCI Center Core Grant for Vision ResearchP30EY034070 · NEI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Vladimir Jivkov Kefalov · 2022 to 2026
$3.7M
Development and function of hypothalamic Lhx6-positive neuronsR01MH126676 · NIMH · JOHNS HOPKINS UNIVERSITY · PI BLACKSHAW, SETH · 2021 to 2025
$2.0M
Identifying gene regulatory networks controlling photoreceptor specification by transcriptomic and epigenomic analysis of retinal development in cone-dominant retinaR21EY032281 · NEI · JOHNS HOPKINS UNIVERSITY · PI BLACKSHAW, SETH · 2021 to 2022
$444k
Comparative Single Cell Profiling of Retinal DevelopmentF31EY031942 · NEI · JOHNS HOPKINS UNIVERSITY · PI WEIR, KURT L · 2021 to 2022
$68k
NEI NIH HHS F31 EY031942NEI NIH HHS F31EY031942NEI NIH HHS P30 EY034070NEI NIH HHS R21 EY032281NEI NIH HHS R24 EY027283NEI NIH HHS R24EY027283NEI NIH HHS U24 EY029891NIMH NIH HHS R01 MH126676
6 · The paper itself

Abstract

Torpor encompasses diverse adaptations to extreme environmental stressors such as hibernation, aestivation, brumation, and daily torpor. Here we introduce StrokeofGenus, an analytic pipeline that identifies distinct transcriptomic states and shared gene expression patterns across studies, tissues, and species. We use StrokeofGenus to study multiple and diverse forms of torpor from publicly-available RNA-seq datasets that span eight species and two classes. We identify three transcriptionally distinct states during the cycle of heterothermia: euthermia, torpor, and interbout arousal. We also identify torpor-specific gene expression patterns that are shared both across tissues and between species with over three hundred million years of evolutionary divergence. We further demonstrate the general sharing of gene expression patterns in multiple forms of torpor, implying a common evolutionary origin for this process. Although here we apply StrokeofGenus to analysis of torpor, it can be used to interrogate any other complex physiological processes defined by transient transcriptomic states.

Indexed as

TorporTranscriptomeVertebratesAnimalsBiological EvolutionGene Expression ProfilingGene Expression RegulationHibernation

Identifiers

PMID39420030
PMCPMC11487170

What Socratic holds

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LicenceCC BY
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Registered trials

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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.