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pmid:35341046

Relationship between circadian genes and memory impairment caused by sleep deprivation.

Peng Ke · Chengjie Zheng · Feng Liu · LinJie Wu · Yijie Tang · Yanqin Wu · Dongdong Lv · Huangli Chen · Lin Qian · Xiaodan Wu · Kai Zeng

PeerJ · 2022 doi:10.7717/peerj.13165

Paper

complete

Experiment

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Data

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title
Relationship between circadian genes and memory impairment caused by sleep deprivation.
doi
10.7717/peerj.13165
pmid
35341046
authors array · 11 items
[0]
Peng Ke
[1]
Chengjie Zheng
[2]
Feng Liu
[3]
LinJie Wu
[4]
Yijie Tang
[5]
Yanqin Wu
[6]
Dongdong Lv
[7]
Huangli Chen
[8]
Lin Qian
[9]
Xiaodan Wu
[10]
Kai Zeng
journal
PeerJ
year
2022
abstract
Background: Sleep deprivation (SD)-induced cognitive impairment is highly prevalent worldwide and has attracted widespread attention. The temporal and spatial oscillations of circadian genes are severely disturbed after SD, leading to a progressive loss of their physiological rhythms, which in turn affects memory function. However, there is a lack of research on the role of circadian genes and memory function after SD. Therefore, the present study aims to investigate the relationship between circadian genes and memory function and provide potential therapeutic insights into the mechanism of SD-induced memory impairment. Methods: Gene expression profiles of GSE33302 and GSE9442 from the Gene Expression Omnibus (GEO) were applied to identify differentially expressed genes (DEGs). Subsequently, both datasets were subjected to Gene Set Enrichment Analysis (GSEA) to determine the overall gene changes in the hippocampus and brain after SD. A Gene Oncology (GO) analysis and Protein-Protein Interaction (PPI) analysis were employed to explore the genes related to circadian rhythm, with their relationship and importance determined through a correlation analysis and a receiver operating characteristic curve (ROC), respectively. The water maze experiments detected behavioral changes related to memory function in SD rats. The expression of circadian genes in several critical organs such as the brain, heart, liver, and lungs and their correlation with memory function was investigated using several microarrays. Finally, changes in the hippocampal immune environment after SD were analyzed using the CIBERSORT in R software. Results: The quality of the two datasets was very good. After SD, changes were seen primarily in genes related to memory impairment and immune function. Genes related to circadian rhythm were highly correlated with engagement in muscle structure development and circadian rhythm. Seven circadian genes showed their potential therapeutic value in SD. Water maze experiments confirmed that SD exacerbates memory impairment-related behaviors, including prolonged escape latencies and reduced numbers of rats crossing the platform. The expression of circadian genes was verified, while some genes were also significant in the heart, liver, and lungs. All seven circadian genes were also associated with memory markers in SD. The contents of four immune cells in the hippocampal immune environment changed after SD. Seven circadian genes were related to multiple immune cells. Conclusions: In the present study, we found that SD leads to memory impairment accompanied by changes in circadian rhythm-related genes. Seven circadian genes play crucial roles in memory impairment after SD. Naïve B cells and follicular helper T cells are closely related to SD. These findings provide new insights into the treatment of memory impairment caused by SD.
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sections[8] "Correlation of circadian rhythm-related genes with their diagnostic value" paragraph 2
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In the R software, a Pearson correlation analysis revealed the relationship among the circadian rhythm-related genes.
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In the present study, we found that SD leads to memory impairment accompanied by changes in circadian rhythm-related genes.
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In the present study, we found that SD leads to memory impairment accompanied by changes in circadian rhythm-related genes.
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group_sizes
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group_sizes_basis
null
platform
1261
taxon
Mus musculus
title
Molecular correlates of sleep deprivation in the brain of three inbred mouse strains in an around-the-clock experiment
resolution_checked_at
2026-11-01T18:06:44Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
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note
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sample_count
555
group_sizes
null
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null
platform
6244
taxon
Homo sapiens
title
Exploring gene expression biomarker candidates for neurobehavioral impairment from total sleep deprivation
resolution_checked_at
2026-11-01T18:06:44Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
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analysis object · 4 fields
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complete
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[0] object · 10 fields
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method-1
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correlation_analysis
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pearson
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Correlation analysis
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pearson_r
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parameters object · 0 fields
data_shapes array · 1 item
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paired_numeric_columns
evidence object · 3 fields
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1
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quote
In the R software, a Pearson correlation analysis revealed the relationship among the circadian rhythm-related genes.
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method-2
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parameters object · 0 fields
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evidence object · 3 fields
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0.7
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medium
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Protein-Protein Interaction
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gaps array · 0 items
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complete
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[0] object · 6 fields
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data object · 6 fields
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true
accessions array · 7 items
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GSE33302
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GSE9442
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GSE98582
[3]
GSE42323
[4]
GSE92913
[5]
GSE42324
[6]
GSE34424
resolved_accessions array · 7 items
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GSE33302
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GSE9442
[2]
GSE98582
[3]
GSE42323
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GSE92913
[5]
GSE42324
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GSE34424
statements array · 1 item
[0]
The raw data are available in the Supplementary Files.
basis
The paper names GSE33302, GSE9442, GSE98582, GSE42323, GSE92913, GSE42324, GSE34424 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
can_run object · 3 fields
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pearson_r
assets array · 2 items
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source:pmid:35341046
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data:geo:GSE33302
steps array · 1 item
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run_analysis
must_build object · 5 fields
dsl_operations array · 0 items
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readers array · 0 items
capabilities array · 0 items
data_gaps array · 1 item
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data:geo:GSE33302
gaps array · 0 items
review object · 5 fields
state
partial
machine_critique object · 5 fields
kind
extraction_review
reader object · 5 fields
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MiniMax-M3.1-Flash
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minimax
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2026-11-01T17:39:38Z
independence
single_reader
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stages array · 1 item
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execution object · 5 fields
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gaps array · 1 item
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provenance object · 7 fields
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pmid:35341046
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paper
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pmid:35341046
[1] object · 3 fields
id
source:pmid:35341046
type
manuscript
label
PMID 35341046 full text
[2] object · 3 fields
id
data:geo:GSE33302
type
dataset
label
GEO GSE33302
activities array · 3 items
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pmid:35341046
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source:pmid:35341046
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PMID 35341046 full text
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data:geo:GSE33302
type
dataset
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GEO GSE33302
agent
agent:corpus-assay-engine
[1] object · 4 fields
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activity-read-35341046
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used array · 1 item
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agent:minimax-reader
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id
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used array · 1 item
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agent:corpus-assay-engine
agents array · 2 items
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agent:corpus-assay-engine
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dsl_catalogue_fingerprint
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lineage object · 4 fields
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gaps array · 18 items
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asset:data:geo:GSE33302 licence not read
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asset:data:geo:GSE33302 not downloaded
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asset:data:geo:GSE34424 licence not read
[3]
asset:data:geo:GSE34424 not downloaded
[4]
asset:data:geo:GSE42323 licence not read
[5]
asset:data:geo:GSE42323 not downloaded
[6]
asset:data:geo:GSE42324 licence not read
[7]
asset:data:geo:GSE42324 not downloaded
[8]
asset:data:geo:GSE92913 licence not read
[9]
asset:data:geo:GSE92913 not downloaded
[10]
asset:data:geo:GSE9442 licence not read
[11]
asset:data:geo:GSE9442 not downloaded
[12]
asset:data:geo:GSE98582 licence not read
[13]
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execution.not_run
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review.human_critique
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review.machine_critique
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assay_lexicon
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evidence array · 4 items
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ral changes related to memory function in SD rats. The expression of circadian genes in severa
[1]
nged escape latencies and reduced numbers of rats crossing the platform. The expression of cir
[2]
rinciple of minimum sample size (n = 5). The rats were acclimated to the environment for two weeks.
[3]
in both groups moved, ate, and drank freely in the rat SD chamber with the SD apparatus. In the sle
order_basis
paper_text_order:1368
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In the R software, a Pearson correlation analysis revealed the relationship among the circadian rhythm-related genes.
order_basis
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:35341046", "kind": "science-record", "revision": 4, "content_hash": "sha256:95b7c4744149521982d890c47a1e6803cf28e8e310946cc73410939a1bf8a39a", "created_at": "2026-11-01T18:14:08Z", "updated_at": "2026-11-01T22:06:10Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Relationship between circadian genes and memory impairment caused by sleep deprivation.", "doi": "10.7717/peerj.13165", "pmid": "35341046", "authors": ["Peng Ke", "Chengjie Zheng", "Feng Liu", "LinJie Wu", "Yijie Tang", "Yanqin Wu", "Dongdong Lv", "Huangli Chen", "Lin Qian", "Xiaodan Wu", "Kai Zeng"], "journal": "PeerJ", "year": 2022, "abstract": "Background: Sleep deprivation (SD)-induced cognitive impairment is highly prevalent worldwide and has attracted widespread attention. The temporal and spatial oscillations of circadian genes are severely disturbed after SD, leading to a progressive loss of their physiological rhythms, which in turn affects memory function. However, there is a lack of research on the role of circadian genes and memory function after SD. Therefore, the present study aims to investigate the relationship between circadian genes and memory function and provide potential therapeutic insights into the mechanism of SD-induced memory impairment.\nMethods: Gene expression profiles of GSE33302 and GSE9442 from the Gene Expression Omnibus (GEO) were applied to identify differentially expressed genes (DEGs). Subsequently, both datasets were subjected to Gene Set Enrichment Analysis (GSEA) to determine the overall gene changes in the hippocampus and brain after SD. A Gene Oncology (GO) analysis and Protein-Protein Interaction (PPI) analysis were employed to explore the genes related to circadian rhythm, with their relationship and importance determined through a correlation analysis and a receiver operating characteristic curve (ROC), respectively. The water maze experiments detected behavioral changes related to memory function in SD rats. The expression of circadian genes in several critical organs such as the brain, heart, liver, and lungs and their correlation with memory function was investigated using several microarrays. Finally, changes in the hippocampal immune environment after SD were analyzed using the CIBERSORT in R software.\nResults: The quality of the two datasets was very good. After SD, changes were seen primarily in genes related to memory impairment and immune function. Genes related to circadian rhythm were highly correlated with engagement in muscle structure development and circadian rhythm. Seven circadian genes showed their potential therapeutic value in SD. Water maze experiments confirmed that SD exacerbates memory impairment-related behaviors, including prolonged escape latencies and reduced numbers of rats crossing the platform. The expression of circadian genes was verified, while some genes were also significant in the heart, liver, and lungs. All seven circadian genes were also associated with memory markers in SD. The contents of four immune cells in the hippocampal immune environment changed after SD. Seven circadian genes were related to multiple immune cells.\nConclusions: In the present study, we found that SD leads to memory impairment accompanied by changes in circadian rhythm-related genes. Seven circadian genes play crucial roles in memory impairment after SD. Naïve B cells and follicular helper T cells are closely related to SD. These findings provide new insights into the treatment of memory impairment caused by SD.", "claims": [{"id": "claim-method", "statement": "In the R software, a Pearson correlation analysis revealed the relationship among the circadian rhythm-related genes.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35341046", "locator": "sections[8] \"Correlation of circadian rhythm-related genes with their diagnostic value\" paragraph 2", "quote": "In the R software, a Pearson correlation analysis revealed the relationship among the circadian rhythm-related genes."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The raw data are available in the Supplementary Files.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35341046", "locator": "sections[32] \"Data Availability\" paragraph 2", "quote": "The raw data are available in the Supplementary Files."}], "state": "complete"}, {"id": "claim-target-result", "statement": "In the present study, we found that SD leads to memory impairment accompanied by changes in circadian rhythm-related genes.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:35341046", "locator": "sections[0] \"Abstract\" paragraph 4", "quote": "In the present study, we found that SD leads to memory impairment accompanied by changes in circadian rhythm-related genes."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "In the present study, we found that SD leads to memory impairment accompanied by changes in circadian rhythm-related genes.", "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:35341046"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE33302"], "outputs": ["the source data with its repository provenance"], "instruments": [], "reagents": []}, {"id": "run_analysis", "order": 3, "name": "Run the published analysis", "kind": "analysis", "state": "complete", "blocked_on": null, "description": "Apply the paper's statistical method to the resolved series and compare the result with the published target.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE33302"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:35341046", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.7717/peerj.13165", "sha256": 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