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pmid:36171891

The regulatory network of potential transcription factors and MiRNAs of mitochondria-related genes for sarcopenia.

Wanrui Fu · Guzailinuer Kadeer · Yaqi He · Ying Feng

Frontiers in genetics · 2022 doi:10.3389/fgene.2022.975886

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complete

Experiment

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Data

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Analysis

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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title
The regulatory network of potential transcription factors and MiRNAs of mitochondria-related genes for sarcopenia.
doi
10.3389/fgene.2022.975886
pmid
36171891
authors array · 4 items
[0]
Wanrui Fu
[1]
Guzailinuer Kadeer
[2]
Yaqi He
[3]
Ying Feng
journal
Frontiers in genetics
year
2022
abstract
Background: Mitochondrial dysfunction is a significant contributor to sarcopenia, but the mechanism remains unclear. Methods: In the present study, we downloaded GSE117525 and GSE8479 datasets from Gene Expression Omnibus (GEO), then the weighted correlation network analysis (WGCNA) was used to construct scale-free co-expression networks respectively. The key genes of aging muscle were obtained by overlapping key modules of two networks. Receiver operating characteristic (ROC) curve was drawn to explore the diagnostic efficacy of key genes. Finally, a transcription factor-key gene network was constructed based on ChEA3 platform and hTFtarget database, and a miRNA-key gene network was constructed using starBase and the multimiR R package. Results: The most positively or negatively correlated modules of the two datasets were identified, and genes related to oxidative phosphorylation and mitochondrial ribosomal proteins were identified as key genes. The diagnostic values were confirmed with ROC curves by self-verification (GSE117525 and GSE8479) and external verification (GSE47881). Then, Yin Yang 1 (YY1) was identified as the most important transcription factor of the transcription factor-key gene network. In addition, miRNAs related to key genes were also predicted. Conclusion: The findings of the present study provide a novel insight into the pathological mechanism of sarcopenia.
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In the present study, we downloaded GSE117525 and GSE8479 datasets from Gene Expression Omnibus (GEO), then the weighted correlation network analysis (WGCNA) was used to construct scale-free co-expression networks respectively.
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In the present study, we downloaded GSE117525 and GSE8479 datasets from Gene Expression Omnibus (GEO), then the weighted correlation network analysis (WGCNA) was used to construct scale-free co-expression networks respectively.
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The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.
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Weighted gene co-expression network analysis identified 29 positively regulating and 160 negatively regulating genes, with the negatively regulating genes associated with mitochondrial respiration, oxidative phosphorylation, and related pathways.
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sections[13] "Identification of the shared pathways" paragraph 2
quote
Using the GO and KEGG enrichment analyses, we further explored the common regulatory pathways that 29 positively-regulating and 160 negatively-regulating genes screened by WGCNA respectively.
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sections[13] "Identification of the shared pathways" paragraph 2
quote
As for the negatively-regulating genes, the GO analysis showed that biological processes (BP) were enriched in cellular respiration, ATP metabolic process, mitochondrial electron transport, NADH to ubiquinone as well as fatty acid metabolic process, and cellular composition (CC) terms were enriched in mitochondrial matrix and NADH dehydrogenase complex, and molecular functions (MF) were enriched in electron transfer activity, and NADH dehydrogenase activity (Figure 2A).
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Weighted gene co-expression network analysis identified 29 positively regulating and 160 negatively regulating genes, with the negatively regulating genes associated with mitochondrial respiration, oxidative phosphorylation, and related pathways.
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Expression of protocadherin gamma in skeletal muscle tissue is associated with age and muscle weakness
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DERBY BBSRC RET Study: Impact of resistance exercise on human skeletal muscle gene expression
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GSM210352
[64]
GSM210353
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65
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null
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null
platform
2700
taxon
Homo sapiens
title
Resistance Exercise Reverses Aging in Human Skeletal Muscle
resolution_checked_at
2026-11-01T18:46:34Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
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[3]
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[4]
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state
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Network / pathway analysis
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quote
protein-protein interaction
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id
method-2
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null
specific
null
label
weighted correlation network analysis (WGCNA)
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evidence object · 3 fields
score
1
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quote
In the present study, we downloaded GSE117525 and GSE8479 datasets from Gene Expression Omnibus (GEO), then the weighted correlation network analysis (WGCNA) was used to construct scale-free co-expression networks respectively.
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method.reader_named_unmapped
capability object · 3 fields
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complete
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[7]
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[8]
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candidate
Automated Assays Laravel application and simulated adapters
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complete
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nothing:replicable_now
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pathway_enrich
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basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: ppi_network.
capability object · 4 fields
tier
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capability:computational_analysis
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owned
basis
The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here.
data object · 6 fields
tier
R1
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[0]
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resolved_accessions array · 3 items
[0]
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GSE47881
statements array · 1 item
[0]
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.
basis
The paper names GSE117525, GSE8479, GSE47881 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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pathway_enrich
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[1]
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run_analysis
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data:geo:GSE117525
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partial
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extraction_review
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MiniMax-M3.1-Flash
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minimax
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minimax
read_at
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independence
single_reader
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method
verbatim
availability
verbatim
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5
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8320
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264
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id
extraction
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complete
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MiniMax-M3.1-Flash
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minimax
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[2]
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not_run
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null
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pmid:36171891
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paper
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pmid:36171891
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source:pmid:36171891
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manuscript
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PMID 36171891 full text
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data:geo:GSE117525
type
dataset
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GEO GSE117525
activities array · 3 items
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id
activity-reading-sci-2026-11-01
type
classification
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pmid:36171891
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paper
label
pmid:36171891
[1] object · 3 fields
id
source:pmid:36171891
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manuscript
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PMID 36171891 full text
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data:geo:GSE117525
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dataset
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GEO GSE117525
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agent:corpus-assay-engine
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activity-read-36171891
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extraction
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source:pmid:36171891
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agent:minimax-reader
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activity-resolve-GSE117525
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agent:corpus-assay-engine
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agent:corpus-assay-engine
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agent:minimax-reader
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343fb30756ba6ec3
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lineage object · 4 fields
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[3]
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[5]
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:36171891", "kind": "science-record", "revision": 4, "content_hash": "sha256:04d523ceb751841d19679d5a8077c98fe82c73a2179e4191148140549db7f44d", "created_at": "2026-11-01T18:15:27Z", "updated_at": "2026-11-01T22:07:39Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "The regulatory network of potential transcription factors and MiRNAs of mitochondria-related genes for sarcopenia.", "doi": "10.3389/fgene.2022.975886", "pmid": "36171891", "authors": ["Wanrui Fu", "Guzailinuer Kadeer", "Yaqi He", "Ying Feng"], "journal": "Frontiers in genetics", "year": 2022, "abstract": "Background: Mitochondrial dysfunction is a significant contributor to sarcopenia, but the mechanism remains unclear. Methods: In the present study, we downloaded GSE117525 and GSE8479 datasets from Gene Expression Omnibus (GEO), then the weighted correlation network analysis (WGCNA) was used to construct scale-free co-expression networks respectively. The key genes of aging muscle were obtained by overlapping key modules of two networks. Receiver operating characteristic (ROC) curve was drawn to explore the diagnostic efficacy of key genes. Finally, a transcription factor-key gene network was constructed based on ChEA3 platform and hTFtarget database, and a miRNA-key gene network was constructed using starBase and the multimiR R package. Results: The most positively or negatively correlated modules of the two datasets were identified, and genes related to oxidative phosphorylation and mitochondrial ribosomal proteins were identified as key genes. The diagnostic values were confirmed with ROC curves by self-verification (GSE117525 and GSE8479) and external verification (GSE47881). Then, Yin Yang 1 (YY1) was identified as the most important transcription factor of the transcription factor-key gene network. In addition, miRNAs related to key genes were also predicted. Conclusion: The findings of the present study provide a novel insight into the pathological mechanism of sarcopenia.", "claims": [{"id": "claim-method", "statement": "In the present study, we downloaded GSE117525 and GSE8479 datasets from Gene Expression Omnibus (GEO), then the weighted correlation network analysis (WGCNA) was used to construct scale-free co-expression networks respectively.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36171891", "locator": "sections[0] \"Abstract\" paragraph 2", "quote": "In the present study, we downloaded GSE117525 and GSE8479 datasets from Gene Expression Omnibus (GEO), then the weighted correlation network analysis (WGCNA) was used to construct scale-free co-expression networks respectively."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36171891", "locator": "sections[20] \"Data availability statement\" paragraph 2", "quote": "The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author."}], "state": "complete"}, {"id": "claim-target-result", "statement": "Weighted gene co-expression network analysis identified 29 positively regulating and 160 negatively regulating genes, with the negatively regulating genes associated with mitochondrial respiration, oxidative phosphorylation, and related pathways.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:36171891", "locator": "sections[13] \"Identification of the shared pathways\" paragraph 2", "quote": "Using the GO and KEGG enrichment analyses, we further explored the common regulatory pathways that 29 positively-regulating and 160 negatively-regulating genes screened by WGCNA respectively."}, {"asset": "source:pmid:36171891", "locator": "sections[13] \"Identification of the shared pathways\" paragraph 2", "quote": "As for the negatively-regulating genes, the GO analysis showed that biological processes (BP) were enriched in cellular respiration, ATP metabolic process, mitochondrial electron transport, NADH to ubiquinone as well as fatty acid metabolic process, and cellular composition (CC) terms were enriched in mitochondrial matrix and NADH dehydrogenase complex, and molecular functions (MF) were enriched in electron transfer activity, and NADH dehydrogenase activity (Figure 2A)."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "Weighted gene co-expression network analysis identified 29 positively regulating and 160 negatively regulating genes, with the negatively regulating genes associated with mitochondrial respiration, oxidative phosphorylation, and related pathways.", "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:36171891"], "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:GSE117525"], "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:GSE117525"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:36171891", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.3389/fgene.2022.975886", "sha256": 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