Journals / Black Sea Journal of Agriculture / 2026 / Cilt: 8 Sayı: 4

Genome-Wide in silico Analysis and Identification of Bos taurus SOX Gene Family

Emre İlhan(ERZURUM TECHNICAL UNIVERSITY)0000-0002-8404-7900
Yusuf Ziya Güzey(Hatay Mustafa Kemal Üniversitesi)0000-0002-4900-6038
Pages
563–569
Publication Date
2025-07-15
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The findings of this research offer a valuable resource for gaining a deeper insight into the molecular foundation of the SOX gene family in Bos taurus.

📌 3 Key Takeaways

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Objective & Hypothesis:The SOX (SRY-box transcription factors) gene family is defined by the presence of the HMG-box (High-mobility group) domain, which was first discovered in the SRY (sex-determining region on the Y chromosome) gene located on the Y chromosome, and plays a vital role in the initiation of male sex determination.
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Key Findings & Data:A total of 15 SOX proteins were identified in the Bos taurus genome.
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Conclusion & Impact:The findings of this research offer a valuable resource for gaining a deeper insight into the molecular foundation of the SOX gene family in Bos taurus.
🔬Design:Araştırma Makalesi
📍Scope:Comprehensive Sample
⚙️Variables:Bos taurus · SOX gene · in silico

Abstract

The SOX (SRY-box transcription factors) gene family is defined by the presence of the HMG-box (High-mobility group) domain, which was first discovered in the SRY (sex-determining region on the Y chromosome) gene located on the Y chromosome, and plays a vital role in the initiation of male sex determination. The purpose of this study was to genome-wide identify and characterize SOX gene family members in silico in Bos taurus. A total of 15 SOX proteins were identified in the Bos taurus genome. These proteins weigh between 26.49 (Bt-SOX-14) and 93.35 (Bt-SOX-6) kDa and have theoretical isoelectric points ranging from 4.95-9.85. As a result of phylogenetic analyses, Bt-SOX proteins and SOX proteins of Mus musculus and Homo sapiens species were clustered in 7 main groups. Segmental duplication was also detected between Bt-SOX-14/Bt-SOX-21, Bt-SOX-5/Bt-SOX-6, Bt-SOX-9/Bt-SOX-10 and Bt-SOX-4/Bt-SOX-11 gene pairs. On the other hand, according to in silico gene expression, Bt-SOX genes exhibited different expression profiles in different tissues and were found to have the highest expression in brain and testicular tissues. This indicates that the majority of Bt-SOX genes have tissue-specific expression. The findings of this research offer a valuable resource for gaining a deeper insight into the molecular foundation of the SOX gene family in Bos taurus.

Özet

The SOX (SRY-box transcription factors) gene family is defined by the presence of the HMG-box (High-mobility group) domain, which was first discovered in the SRY (sex-determining region on the Y chromosome) gene located on the Y chromosome, and plays a vital role in the initiation of male sex determination. The purpose of this study was to genome-wide identify and characterize SOX gene family members in silico in Bos taurus. A total of 15 SOX proteins were identified in the Bos taurus genome. These proteins weigh between 26.49 (Bt-SOX-14) and 93.35 (Bt-SOX-6) kDa and have theoretical isoelectric points ranging from 4.95-9.85. As a result of phylogenetic analyses, Bt-SOX proteins and SOX proteins of Mus musculus and Homo sapiens species were clustered in 7 main groups. Segmental duplication was also detected between Bt-SOX-14/Bt-SOX-21, Bt-SOX-5/Bt-SOX-6, Bt-SOX-9/Bt-SOX-10 and Bt-SOX-4/Bt-SOX-11 gene pairs. On the other hand, according to in silico gene expression, Bt-SOX genes exhibited different expression profiles in different tissues and were found to have the highest expression in brain and testicular tissues. This indicates that the majority of Bt-SOX genes have tissue-specific expression. The findings of this research offer a valuable resource for gaining a deeper insight into the molecular foundation of the SOX gene family in Bos taurus.

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Cite This Article

İlhan, E., Güzey, Y. Z. (2025). Genome-Wide in silico Analysis and Identification of Bos taurus SOX Gene Family. Black Sea Journal of Agriculture, Cilt: 8 Sayı: 4, 563–569. https://doi.org/10.47115/bsagriculture.1719387

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References (16)

  1. Abdullah M, Saif-ur Rehman M, Nawaz-ul Rehman MS, AlKahtane AA, Al-Hazani TM, Hassan F, Rehman S. 2023. Genome-wide identification, evolutionary and mutational analysis of the buffalo SOX gene family. Animals, 13: 2246. https://doi.org/10.3390/ani13142246
  2. Akinyemi MO, Finucan J, Grytsay A, Osaiyuwu OH, Adegbaju MS, Ogunade IM, Thomas BN, Peters SO, Morenikeji OB. 2022. Molecular evolution and inheritance pattern of SOX gene family among Bovidae. Genes, 13: 1783. https://doi.org/10.3390/genes13101783
  3. Anonymous. 2025. World population projected to reach 9.8 billion in 2050, and 11.2 billion in 2100. URL: https://www.un.org/en/desa/world-population-projected-reach-98-billion-2050-and-112-billion-2100 (accessed date: July 13, 2025).
  4. Bailey TL, Williams N, Misleh C, Li WW. 2006. MEME: discovering and analyzing DNA and protein sequence motifs. Nucleic Acids Res, 34(Web Server issue): W369-373. https://doi.org/10.1093/nar/gkl198
  5. Crooks GE, Hon G, Chandonia JM, Brenner SE. 2004. WebLogo: a sequence logo generator. Genome Res, 14(6): 1188-1190.
  6. Fu Y, Khan MF, Wang Y, Parveen S, Sultana M, Liu Q, Shafique L. 2024. In silico analysis: molecular characterization and evolutionary study of CLCN gene family in buffalo. Genes, 15: 1163. https://doi.org/10.3390/genes15091163
  7. Guo AY, Zhu QH, Chen X, Luo JC. 2007. GSDS: a gene structure display server. Yi Chuan (Hereditas), 29(8): 1023-1026.
  8. Haseeb A, Lefebvre V. 2019. The SOX transcription factors—SOX8, SOX9 and SOX10—share a bi-partite transactivation mechanism. Nucleic Acids Res, 47: 6917-6931.
  9. Ilhan E, Büyük B, Inal B. 2018. Transcriptome-scale characterization of salt responsive bean TCP transcription factors. Gene, 642: 64-73. https://doi.org/10.1016/j.gene.2017.11.021
  10. Jiang L, Bi D, Ding H, Wu X, Zhu R, Zeng J, Yang X, Kan X. 2019. Systematic identification and evolution analysis of SOX genes in Coturnix japonica based on comparative genomics. Genes, 10: 314. https://doi.org/10.3390/genes10040314
  11. Quevillon E, Silventoinen V, Pillai S, Harte N, Mulder N, Apweiler R, Lopez R. 2005. InterProScan: protein domains identifier. Nucleic Acids Res, 33(Web Server issue): W116-120. https://doi.org/10.1093/nar/gki442
  12. Rexroad C, Vallet J, Matukumalli LK, Reecy J, Bickhart D, Blackburn H, Boggess M, Cheng H, Clutter A, Cockett N, Ernst C, Fulton JE, Liu J, Lunney J, Neigbergs H, Purcell C, Smith TPL, Sonstegard T, Taylor J, Telugu B, Van Eenennaam A, Van Tassell CP, Wells K. 2019. Genome to phenome: improving animal health, production, and well-being – a new USDA blueprint for animal genome research 2018–2027. Front Genet, 10: 1-29. https://doi.org/10.3389/fgene.2019.00327
  13. Smits P, Li P, Mandel J, Zhang Z, Deng JM, Behringer RR, de Crombrugghe B, Lefebvre V. 2001. The transcription factors L-SOX5 and SOX6 are essential for cartilage formation. Dev Cell, 1: 277-290.
  14. Voorrips RE. 2002. MapChart: software for the graphical presentation of linkage maps and QTLs. J Hered, 93(1): 77-78. https://doi.org/10.1093/jhered/93.1.77
  15. Yang Z, Gu S, Wang X, Li W, Tang Z, Xu C. 2008. Molecular evolution of the CPP-like gene family in plants: insights from comparative genomics of Arabidopsis and rice. J Mol Evol, 67(3): 266-277. https://doi.org/10.1007/s00239-008-9143-z
  16. Zhang S, Chen X, Wang M, Zhang W, Pan J, Qin Q, Zhong L, Shao J, Sun M, Jiang H, Bian W. 2018. Genome-wide identification, phylogeny and expressional profile of the SOX gene family in channel catfish (Ictalurus punctatus). Comp Biochem Physiol Part D Genomics Proteomics, 28: 17-26. https://doi.org/10.1016/j.cbd.2018.03.001