Evidence map›Paper›PMID 32896721›Full record

ArticleRedox biology2020

PER1 interaction with GPX1 regulates metabolic homeostasis under oxidative stress.

Qi Sun, Yunxia Yang, Zhongqiu Wang, Xiao Yang, Yan Gao, Yang Zhao, Wenhao Ge, Junhao Liu, Xi Xu, Wei Guan and 4 more

Open access · goldAbstract read
In one paragraph

Article in Redox biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

27 citing papers in PubMed, 47 citations in OpenAlex.

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  12. Helicobacter Pylori-Enhanced hnRNPA2B1 Coordinates with PABPC1 to Promote Non-mAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
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  20. The PRMT6/PARP1/CRL4B Complex Regulates the Circadian Clock and Promotes Breast Tumorigenesis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    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

14 authors at 4 institutions in 1 country.

Qi SunCenter for Molecular Metabolism, Nanjing University of Science & Technology, Nanjing, 210094, China; Key Laboratory of Cardiovascular and Cerebrovascular Diseases, Bengbu Medical College, Bengbu, 233030, China.
Yunxia YangCenter for Molecular Metabolism, Nanjing University of Science & Technology, Nanjing, 210094, China.
Zhongqiu WangAffiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, 210029, China.
Xiao YangCenter for Molecular Metabolism, Nanjing University of Science & Technology, Nanjing, 210094, China.
Yan GaoCenter for Molecular Metabolism, Nanjing University of Science & Technology, Nanjing, 210094, China.
Yang ZhaoCenter for Molecular Metabolism, Nanjing University of Science & Technology, Nanjing, 210094, China.
Wenhao GeCenter for Molecular Metabolism, Nanjing University of Science & Technology, Nanjing, 210094, China.
Junhao LiuCenter for Molecular Metabolism, Nanjing University of Science & Technology, Nanjing, 210094, China.
Xi XuCenter for Molecular Metabolism, Nanjing University of Science & Technology, Nanjing, 210094, China.
Wei GuanThe Second Hospital of Nanjing, Nanjing Medical University, Nanjing, 210003, China.
Dan WengCenter for Molecular Metabolism, Nanjing University of Science & Technology, Nanjing, 210094, China.
Shiming WangCenter for Molecular Metabolism, Nanjing University of Science & Technology, Nanjing, 210094, China.
Junsong WangCenter for Molecular Metabolism, Nanjing University of Science & Technology, Nanjing, 210094, China.
Jianfa ZhangCenter for Molecular Metabolism, Nanjing University of Science & Technology, Nanjing, 210094, China. Electronic address: jfzhang@mail.njust.edu.cn.
Nanjing University of Science and Technology · CNBengbu Medical College · CNNanjing University of Chinese Medicine · CNSecond Affiliated Hospital of Nanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolism serves mammalian feeding and active behavior, and is controlled by circadian clock. The molecular mechanism by which clock factors regulate metabolic homeostasis under oxidative stress is unclear. Here, we have characterized that the daily oxygen consumption rhythm was deregulated in Per1 deficient mice. Per1 deficiency impaired daily mitochondrial dynamics and deregulated cellular GPx-related ROS fluctuations in the peripheral organs. We identified that PER1 enhanced GPx activity through PER1/GPX1 interaction in cytoplasm, consequently improving the oxidative phosphorylation efficiency of mitochondria. Per1 expression was specifically elevated in the fasting peripheral organs for protecting mitochondrial from oxidation stress. These observations reveal that Per1-driven mitochondrial dynamics is a critical effector mechanism for the regulation of mitochondrial function in response to oxidation stress.

Indexed as

Circadian ClocksOxidative StressPeriod Circadian ProteinsAnimalsCircadian RhythmGlutathione PeroxidaseGlutathione Peroxidase GPX1HomeostasisMiceTranscription FactorsGlutathione PeroxidaseGlutathione Peroxidase GPX1Gpx1 protein, mousePer1 protein, mousePeriod Circadian ProteinsTranscription FactorsGPX1Metabolic rhythmOxidation stressPER1ROS

Identifiers

PMID32896721
PMCPMC7484554
OpenAlexW3080507493

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.