Clinical and gonadal transcriptome analysis of 38,XX disorder of sex development pigs
© The Author(s) 2024. Published by Oxford University Press on behalf of Society for the Study of Reproduction. All rights reserved. For permissions, please e-mail: journals.permissionsoup.com..
Pigs serve as a robust animal model for the study of human diseases, notably in the context of disorders of sex development (DSD). This study aims to investigate the phenotypic characteristics and molecular mechanisms underlying the reproductive and developmental abnormalities of 38,XX ovotestis-DSD (OT-DSD) and 38,XX testis-DSD (T-DSD) in pigs. Clinical and transcriptome sequencing analyses were performed on DSD and normal female pigs. Cytogenetic and SRY analyses confirmed that OT/T-DSD pigs exhibited a 38,XX karyotype and lacked the SRY gene. The DSD pigs had higher levels of follicle-stimulating hormone, luteinizing hormone, and progesterone, but lower testosterone levels when compared with normal male pigs. The reproductive organs of OT/T-DSD pigs exhibit abnormal development, displaying both male and female characteristics, with an absence of germ cells in the seminiferous tubules. Sex determination and development-related differentially-expressed genes (DEGs) shared between DSD pigs were identified in the gonads, including WT1, DKK1, CTNNB1, WTN9B, SHOC, PTPN11, NRG1 and NXK3-1. DKK1 is proposed as a candidate gene for investigating the regulatory mechanisms underlying gonadal phenotypic differences between OT-DSD and T-DSD pigs. Consequently, our findings provide insights into the molecular pathogenesis of DSD pigs and present an animal model for studying into DSD in humans.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2024 |
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Erschienen: |
2024 |
Enthalten in: |
Zur Gesamtaufnahme - year:2024 |
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Enthalten in: |
Biology of reproduction - (2024) vom: 26. März |
Sprache: |
Englisch |
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Beteiligte Personen: |
Wu, Jinhua [VerfasserIn] |
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Links: |
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Themen: |
Cytogenetic |
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Anmerkungen: |
Date Revised 26.03.2024 published: Print-Electronic Citation Status Publisher |
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doi: |
10.1093/biolre/ioae046 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM370213319 |
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520 | |a Pigs serve as a robust animal model for the study of human diseases, notably in the context of disorders of sex development (DSD). This study aims to investigate the phenotypic characteristics and molecular mechanisms underlying the reproductive and developmental abnormalities of 38,XX ovotestis-DSD (OT-DSD) and 38,XX testis-DSD (T-DSD) in pigs. Clinical and transcriptome sequencing analyses were performed on DSD and normal female pigs. Cytogenetic and SRY analyses confirmed that OT/T-DSD pigs exhibited a 38,XX karyotype and lacked the SRY gene. The DSD pigs had higher levels of follicle-stimulating hormone, luteinizing hormone, and progesterone, but lower testosterone levels when compared with normal male pigs. The reproductive organs of OT/T-DSD pigs exhibit abnormal development, displaying both male and female characteristics, with an absence of germ cells in the seminiferous tubules. Sex determination and development-related differentially-expressed genes (DEGs) shared between DSD pigs were identified in the gonads, including WT1, DKK1, CTNNB1, WTN9B, SHOC, PTPN11, NRG1 and NXK3-1. DKK1 is proposed as a candidate gene for investigating the regulatory mechanisms underlying gonadal phenotypic differences between OT-DSD and T-DSD pigs. Consequently, our findings provide insights into the molecular pathogenesis of DSD pigs and present an animal model for studying into DSD in humans | ||
650 | 4 | |a Journal Article | |
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650 | 4 | |a cytogenetic | |
650 | 4 | |a mRNA transcriptome | |
650 | 4 | |a phenotype | |
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700 | 1 | |a Zhou, Yi |e verfasserin |4 aut | |
700 | 1 | |a Zhao, Haiquan |e verfasserin |4 aut | |
700 | 1 | |a Yu, Hui |e verfasserin |4 aut | |
700 | 1 | |a Zhong, Bingzhou |e verfasserin |4 aut | |
700 | 1 | |a Yu, Congying |e verfasserin |4 aut | |
700 | 1 | |a Wang, Haoming |e verfasserin |4 aut | |
700 | 1 | |a Yang, Yin |e verfasserin |4 aut | |
700 | 1 | |a Li, Hua |e verfasserin |4 aut | |
700 | 1 | |a Li, Yugu |e verfasserin |4 aut | |
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