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pmid:28623929

The potential regulatory mechanisms of the gonadotropin-releasing hormone in gonadotropin transcriptions identified with bioinformatics analyses.

Wei Xiang · Baoyun Zhang · Fenglin Lv · Guangde Feng · Long Chen · Fang Yang · Ke Zhang · Chunyu Cao · Pingqing Wang · Mingxing Chu

Reproductive biology and endocrinology : RB&E · 2017 doi:10.1186/s12958-017-0264-3

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complete

Experiment

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Data

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:28623929
kind
science-record
content_hash
sha256:4ba0ec8405713c932529961a3300c5b7438f3b63bb17ddc81f5dfd2bbad3f711
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https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json
created_at
2026-11-01T15:40:26Z
updated_at
2026-11-01T21:59:25Z
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paper object · 10 fields
state
complete
title
The potential regulatory mechanisms of the gonadotropin-releasing hormone in gonadotropin transcriptions identified with bioinformatics analyses.
doi
10.1186/s12958-017-0264-3
pmid
28623929
authors array · 10 items
[0]
Wei Xiang
[1]
Baoyun Zhang
[2]
Fenglin Lv
[3]
Guangde Feng
[4]
Long Chen
[5]
Fang Yang
[6]
Ke Zhang
[7]
Chunyu Cao
[8]
Pingqing Wang
[9]
Mingxing Chu
journal
Reproductive biology and endocrinology : RB&E
year
2017
abstract
BACKGROUND: The regulation of gonadotropin synthesis and release by gonadotropin-releasing hormone (GnRH) plays an essential role in the neuroendocrine control of reproduction. However, the mechanisms underlying gonadotropin regulation by GnRH pulse frequency and amplitude are still ambiguous. This study aimed to explore the molecular mechanisms and biological pathways associated with gonadotropin synthesis by GnRH pulse frequencies and amplitudes. METHODS: Using GSE63251 datasets downloaded from the Gene Expression Omnibus (GEO), differentially expressed genes (DEGs) were screened by comparing the RNA expression from the GnRH pulse group, the GnRH tonic group and the control group. Pathway enrichment analyses of DEGs was performed, followed by protein-protein interaction (PPI) network construction. Furthermore, sub-network modules were constructed by ClusterONE and GO function and pathways analysed by DAVID. In addition, the relationship between the metabolic pathways and the GnRH pathway was verified in vitro. RESULTS: In total, 531 common DEGs were identified in GnRH groups, including 290 up-regulated and 241 down-regulated genes. DEGs predominantly enriched in 16 Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways, including 11 up-regulated pathways (signallingsignallingmetabolic pathways, signallingand GnRH signalling pathway) and 5 down-regulated pathways (type II diabetes mellitus). Moreover, FBJ osteosarcoma oncogene (FOS) and jun proto-oncogene (JUN) had higher connectivity degrees in the PPI network. Three modules in the PPI were identified with ClusterONE. The genes in module 1 were significantly enriched in five pathways, including signallingthe insulin resistance and GnRH signalling pathway. The genes in modules 2 and 3 were mainly enriched in metabolic pathways and steroid hormone biosynthesis, respectively. Finally, knockdown leptin receptor (LEPR) and insulin receptor (INSR) reversed the GnRH-modulated metabolic related-gene expression. CONCLUSIONS: The present study revealed the involvement of GnRH in the regulation of gonadotropin biosynthesis and metabolism in the maintenance of reproduction, achieved by bioinformatics analyses. This, indicates that the GnRH signalling pathway played a central linkings role in reproductive function and metabolic balance. In addition, the present study identified the difference response between GnRH pulse and GnRH tone, indicated that abnormal GnRH pulse and amplitude may cause disease, which may provide an improved understanding of the GnRH pathway and a new insight for disease diagnosis and treatment.
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Multiple testing was corrected using the Benjamini–Hochberg [20] procedure to obtain the adjusted P-value.
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sections[4] "Data preprocessing and differential expression analysis" paragraph 2
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Multiple testing was corrected using the Benjamini–Hochberg [20] procedure to obtain the adjusted P-value.
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The datasets used and/or analyzed during the current study available from the corresponding author on reasonable request.
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The datasets used and/or analyzed during the current study available from the corresponding author on reasonable request.
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Regulation of LbetaT2 gonadotrope gene expression by GnRH pulses
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F:5′- GCCGCATCTACATTGACGAC-3′
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[3]
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[5]
6.49E-09
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[1]
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11
[3]
9
[4]
3.60E-04
[5]
0.011371
[5] array · 6 items
[0]
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[3]
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[4]
4.01E-04
[5]
1.00E-03
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p53 signalling pathway
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8.34E-04
[5]
1.90E-03
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0.032455
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Pathways in cancer
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[3]
21
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0.003327
[5]
0.04242
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83
[3]
111
[4]
0.015105
[5]
0.008450594
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[0]
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[1]
Cytokine-cytokine receptor interaction
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19
[3]
11
[4]
0.033202668
[5]
0.048153254
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Adipocytokine signalling pathway
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[3]
8
[4]
0.034984
[5]
0.019396
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Prion diseases
[2]
5
[3]
6
[4]
0.037602
[5]
0.013348
[13] array · 6 items
[0]
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[1]
Viral myocarditis
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8
[3]
9
[4]
0.045733
[5]
0.038737
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11
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11
[4]
0.046921
[5]
0.045341
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ErbB signalling pathway
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7
[3]
9
[4]
0.048712
[5]
0.025918
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[0]
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[1]
Valine, leucine and isoleucine degradation
[2]
8
[3]
0.004814562
[4]
6
[5]
0.049249252
[18] array · 6 items
[0]
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[1]
Oocyte meiosis
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13
[3]
0.006667
[4]
12
[5]
0.03641
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[0]
mmu04914
[1]
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[2]
10
[3]
0.016259
[4]
10
[5]
0.031867499
[20] array · 6 items
[0]
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[2]
7
[3]
0.024595
[4]
8
[5]
0.012683147
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The enriched KEGG pathway of DEGs which exist in pulse GnRH group while not exist in tonic GnRH group
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Pathway enrichment analysis
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Table 3
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The enriched KEGG pathway of DEGs which exist in pulse GnRH group while not exist in tonic GnRH group
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[1]
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[3]
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[3]
0.047944857
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[1]
Calcium signalling pathway
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[3]
0.048934483
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PPI network construction and hub gene identification
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caption
The hub proteins in protein–protein interaction network (top 10)
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[3]
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Functional module analysis
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Enriched pathways of DEGs in sub-network
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6
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section[15]/table-wrap[1]#Tab5
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Multiple testing was corrected using the Benjamini–Hochberg [20] procedure to obtain the adjusted P-value.
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Automated Assays Laravel application and simulated adapters
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basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: anova.
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GSE63251
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The datasets used and/or analyzed during the current study available from the corresponding author on reasonable request.
basis
The paper names GSE63251 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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hormone biosynthesis, respectively. Finally, knockdown leptin receptor (LEPR) and insulin receptor
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:28623929", "kind": "science-record", "revision": 7, "content_hash": "sha256:4ba0ec8405713c932529961a3300c5b7438f3b63bb17ddc81f5dfd2bbad3f711", "created_at": "2026-11-01T15:40:26Z", "updated_at": "2026-11-01T21:59:25Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "The potential regulatory mechanisms of the gonadotropin-releasing hormone in gonadotropin transcriptions identified with bioinformatics analyses.", "doi": "10.1186/s12958-017-0264-3", "pmid": "28623929", "authors": ["Wei Xiang", "Baoyun Zhang", "Fenglin Lv", "Guangde Feng", "Long Chen", "Fang Yang", "Ke Zhang", "Chunyu Cao", "Pingqing Wang", "Mingxing Chu"], "journal": "Reproductive biology and endocrinology : RB&E", "year": 2017, "abstract": "BACKGROUND: The regulation of gonadotropin synthesis and release by gonadotropin-releasing hormone (GnRH) plays an essential role in the neuroendocrine control of reproduction. However, the mechanisms underlying gonadotropin regulation by GnRH pulse frequency and amplitude are still ambiguous. This study aimed to explore the molecular mechanisms and biological pathways associated with gonadotropin synthesis by GnRH pulse frequencies and amplitudes.\nMETHODS: Using GSE63251 datasets downloaded from the Gene Expression Omnibus (GEO), differentially expressed genes (DEGs) were screened by comparing the RNA expression from the GnRH pulse group, the GnRH tonic group and the control group. Pathway enrichment analyses of DEGs was performed, followed by protein-protein interaction (PPI) network construction. Furthermore, sub-network modules were constructed by ClusterONE and GO function and pathways analysed by DAVID. In addition, the relationship between the metabolic pathways and the GnRH pathway was verified in vitro.\nRESULTS: In total, 531 common DEGs were identified in GnRH groups, including 290 up-regulated and 241 down-regulated genes. DEGs predominantly enriched in 16 Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways, including 11 up-regulated pathways (signallingsignallingmetabolic pathways, signallingand GnRH signalling pathway) and 5 down-regulated pathways (type II diabetes mellitus). Moreover, FBJ osteosarcoma oncogene (FOS) and jun proto-oncogene (JUN) had higher connectivity degrees in the PPI network. Three modules in the PPI were identified with ClusterONE. The genes in module 1 were significantly enriched in five pathways, including signallingthe insulin resistance and GnRH signalling pathway. The genes in modules 2 and 3 were mainly enriched in metabolic pathways and steroid hormone biosynthesis, respectively. Finally, knockdown leptin receptor (LEPR) and insulin receptor (INSR) reversed the GnRH-modulated metabolic related-gene expression.\nCONCLUSIONS: The present study revealed the involvement of GnRH in the regulation of gonadotropin biosynthesis and metabolism in the maintenance of reproduction, achieved by bioinformatics analyses. This, indicates that the GnRH signalling pathway played a central linkings role in reproductive function and metabolic balance. In addition, the present study identified the difference response between GnRH pulse and GnRH tone, indicated that abnormal GnRH pulse and amplitude may cause disease, which may provide an improved understanding of the GnRH pathway and a new insight for disease diagnosis and treatment.", "claims": [{"id": "claim-method", "statement": "Multiple testing was corrected using the Benjamini–Hochberg [20] procedure to obtain the adjusted P-value.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:28623929", "locator": "sections[4] \"Data preprocessing and differential expression analysis\" paragraph 2", "quote": "Multiple testing was corrected using the Benjamini–Hochberg [20] procedure to obtain the adjusted P-value."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets used and/or analyzed during the current study available from the corresponding author on reasonable request.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:28623929", "locator": "sections[20] \"ack\" paragraph 1", "quote": "The datasets used and/or analyzed during the current study available from the corresponding author on reasonable request."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": null, "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:28623929"], "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. 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