Evidence map›Paper›PMID 42455861›Full record

ArticlePLoS biology2026

Peroxisomal import is circadian in glia and regulates sleep and lipid metabolism.

Anurag Das, Irma Magaly Rivas-Serna, Ankur Kumar, Lakpa Sherpa, Kerui Huang, Hia Kalita, Marlene Dorneich-Hayes, Ruiqi Liu, Vera C Mazurak, John P Vaughen and 1 more

Abstract read
In one paragraph

Article in PLoS biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Anurag DasDepartment of Genetics, Development, and Cell Biology, Iowa State University, Ames, Iowa, United States of America.ORCID https://orcid.org/0000-0002-2042-6207
Irma Magaly Rivas-SernaDepartment of Agriculture, Food, and Nutritional Science, University of Alberta, Edmonton, Canada.
Ankur KumarDepartment of Genetics, Development, and Cell Biology, Iowa State University, Ames, Iowa, United States of America.
Lakpa SherpaDepartment of Genetics, Development, and Cell Biology, Iowa State University, Ames, Iowa, United States of America.
Kerui HuangDepartment of Genetics, Development, and Cell Biology, Iowa State University, Ames, Iowa, United States of America.
Hia KalitaInterdepartmental MCDB PhD Program, Iowa State University, Ames, Iowa, United States of America.
Marlene Dorneich-HayesDepartment of Genetics, Development, and Cell Biology, Iowa State University, Ames, Iowa, United States of America.
Ruiqi LiuDepartment of Genetics, Development, and Cell Biology, Iowa State University, Ames, Iowa, United States of America.
Vera C MazurakDepartment of Agriculture, Food, and Nutritional Science, University of Alberta, Edmonton, Canada.
John P VaughenDepartment of Anatomy, University of California San Francisco, San Francisco, California, United States of America.
Hua BaiDepartment of Genetics, Development, and Cell Biology, Iowa State University, Ames, Iowa, United States of America.

Funding

Resource Project CoreU41HG000739 · NHGRI · HARVARD UNIVERSITY · PI PERRIMON, NORBERT · 2014 to 2022
$32.3M
Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI KEVIN R COOK · 2014 to 2026
$13.5M
National Metabolomics Data Repository - nextgen Metabolomics WorkbenchU2CDK119886 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SUBRAMANIAM, SHANKAR · 2018 to 2021
$12.7M
Biomedical Data Commons Workbench (BDCW)OT2OD030544 · OD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SUBRAMANIAM, SHANKAR · 2020 to 2024
$3.2M
Web Portal CoreU2CDK119889 · NIDDK · UNIVERSITY OF FLORIDA · PI CONLON, MICHAEL, GARRETT, TIMOTHY J · 2018 to 2021
$1.9M
Role of peroxisome-mitochondrion communication in tissue agingR01AG075156 · NIA · IOWA STATE UNIVERSITY · PI Hua Bai · 2023 to 2026
$1.2M
NHGRI NIH HHS U41 HG000739NIA NIH HHS R01 AG075156NIDDK NIH HHS U2C DK119886NIDDK NIH HHS U2C DK119889NIH HHS OT2 OD030544NIH HHS P40 OD018537
6 · The paper itself

Abstract

Peroxisomes are critical organelles that detoxify cellular waste while also catabolizing and anabolizing lipids. How peroxisomes coordinate protein import and support metabolic functions across complex tissues and timescales remains poorly understood in vivo. Using the Drosophila brain, we discover a striking enrichment of peroxisomes in the neuronal soma and the cortex glia that enwrap them. Unexpectedly, import of peroxisomal proteins into cortex glia, but not neurons, oscillated across time and peaked in the early morning. Rhythmic peroxisomal import in cortex glia autonomously required the circadian clock and Peroxin 5 (Pex5; peroxisomal biogenesis factor 5 homolog), with import persistently elevated in clock mutants. Notably, reducing Pex5 in cortex glia, but not neurons, caused hyperactivity and reduced total sleep. Moreover, brain lipid metabolism was dramatically altered upon Pex5 knockdown, with glia impacting sphingolipids and triacylglycerols, and neurons impacting phospholipids. The cell-type specificity of these Pex5 phenotypes highlights unique roles for peroxisomal import in both sleep and lipid metabolism in the brain.

Indexed as

Circadian RhythmLipid MetabolismNeurogliaPeroxisomesSleepAnimalsBrainCircadian ClocksDrosophila melanogasterDrosophila ProteinsNeuronsPeroxisome-Targeting Signal 1 ReceptorProtein TransportDrosophila ProteinsPeroxisome-Targeting Signal 1 Receptor

Identifiers

PMID42455861
PMCPMC13387613

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.