Identification of hub genes associated with spermatogenesis by bioinformatics analysis

Abstract Spermatogenesis is a complex process related to male infertility. Till now, the critical genes and specific mechanisms have not been elucidated clearly. Our objective was to determine the hub genes that play a crucial role in spermatogenesis by analyzing the differentially expressed genes (...

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Main Authors: Shuang Liu, Yan-chao Bian, Wan-lun Wang, Tong-Jia Liu, Ting Zhang, Yue Chang, Rui Xiao, Chuan-ling Zhang
Format: Article
Language:English
Published: Nature Portfolio 2023-10-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-023-45620-3
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author Shuang Liu
Yan-chao Bian
Wan-lun Wang
Tong-Jia Liu
Ting Zhang
Yue Chang
Rui Xiao
Chuan-ling Zhang
author_facet Shuang Liu
Yan-chao Bian
Wan-lun Wang
Tong-Jia Liu
Ting Zhang
Yue Chang
Rui Xiao
Chuan-ling Zhang
author_sort Shuang Liu
collection DOAJ
description Abstract Spermatogenesis is a complex process related to male infertility. Till now, the critical genes and specific mechanisms have not been elucidated clearly. Our objective was to determine the hub genes that play a crucial role in spermatogenesis by analyzing the differentially expressed genes (DEGs) present in non-obstructive azoospermia (NOA) compared to OA and normal samples using bioinformatics analysis. Four datasets, namely GSE45885, GSE45887, GSE9210 and GSE145467 were used. Functional enrichment analyses were performed on the DEGs. Hub genes were identified based on protein–protein interactions between DEGs. The expression of the hub genes was further examined in the testicular germ cell tumors from the TCGA by the GEPIA and validated by qRT-PCR in the testes of lipopolysaccharide-induced acute orchitis mice with impaired spermatogenesis. A total of 203 DEGs including 34 up-regulated and 169 down-regulated were identified. Functional enrichment analysis showed DEGs were mainly involved in microtubule motility, the process of cell growth and protein transport. PRM2, TEKT2, FSCN3, UBQLN3, SPATS1 and GTSF1L were identified and validated as hub genes for spermatogenesis. Three of them (PRM2, FSCN3 and TEKT2) were significantly down-regulated in the testicular germ cell tumors and their methylation levels were associated with the pathogenesis. In summary, the hub genes identified may be related to spermatogenesis and may act as potential therapeutic targets for NOA and testicular germ cell tumors.
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spelling doaj.art-73e1cadfbc304f1e93712a1278327d722023-10-29T12:20:07ZengNature PortfolioScientific Reports2045-23222023-10-0113111310.1038/s41598-023-45620-3Identification of hub genes associated with spermatogenesis by bioinformatics analysisShuang Liu0Yan-chao Bian1Wan-lun Wang2Tong-Jia Liu3Ting Zhang4Yue Chang5Rui Xiao6Chuan-ling Zhang7Inner Mongolia Key Laboratory of Molecular Pathology, Inner Mongolia Medical UniversityInner Mongolia Key Laboratory of Molecular Pathology, Inner Mongolia Medical UniversityInner Mongolia Key Laboratory of Molecular Pathology, Inner Mongolia Medical UniversityInner Mongolia Key Laboratory of Molecular Pathology, Inner Mongolia Medical UniversityInner Mongolia Key Laboratory of Molecular Pathology, Inner Mongolia Medical UniversityInner Mongolia Key Laboratory of Molecular Pathology, Inner Mongolia Medical UniversityInner Mongolia Key Laboratory of Molecular Pathology, Inner Mongolia Medical UniversityDepartment of Pharmacy, Inner Mongolia Medical UniversityAbstract Spermatogenesis is a complex process related to male infertility. Till now, the critical genes and specific mechanisms have not been elucidated clearly. Our objective was to determine the hub genes that play a crucial role in spermatogenesis by analyzing the differentially expressed genes (DEGs) present in non-obstructive azoospermia (NOA) compared to OA and normal samples using bioinformatics analysis. Four datasets, namely GSE45885, GSE45887, GSE9210 and GSE145467 were used. Functional enrichment analyses were performed on the DEGs. Hub genes were identified based on protein–protein interactions between DEGs. The expression of the hub genes was further examined in the testicular germ cell tumors from the TCGA by the GEPIA and validated by qRT-PCR in the testes of lipopolysaccharide-induced acute orchitis mice with impaired spermatogenesis. A total of 203 DEGs including 34 up-regulated and 169 down-regulated were identified. Functional enrichment analysis showed DEGs were mainly involved in microtubule motility, the process of cell growth and protein transport. PRM2, TEKT2, FSCN3, UBQLN3, SPATS1 and GTSF1L were identified and validated as hub genes for spermatogenesis. Three of them (PRM2, FSCN3 and TEKT2) were significantly down-regulated in the testicular germ cell tumors and their methylation levels were associated with the pathogenesis. In summary, the hub genes identified may be related to spermatogenesis and may act as potential therapeutic targets for NOA and testicular germ cell tumors.https://doi.org/10.1038/s41598-023-45620-3
spellingShingle Shuang Liu
Yan-chao Bian
Wan-lun Wang
Tong-Jia Liu
Ting Zhang
Yue Chang
Rui Xiao
Chuan-ling Zhang
Identification of hub genes associated with spermatogenesis by bioinformatics analysis
Scientific Reports
title Identification of hub genes associated with spermatogenesis by bioinformatics analysis
title_full Identification of hub genes associated with spermatogenesis by bioinformatics analysis
title_fullStr Identification of hub genes associated with spermatogenesis by bioinformatics analysis
title_full_unstemmed Identification of hub genes associated with spermatogenesis by bioinformatics analysis
title_short Identification of hub genes associated with spermatogenesis by bioinformatics analysis
title_sort identification of hub genes associated with spermatogenesis by bioinformatics analysis
url https://doi.org/10.1038/s41598-023-45620-3
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