Identification of piRNA Expression Profiles in Vitiligo
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Published:2024-08
Issue:4
Volume:50
Page:1365-1375
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ISSN:1068-1620
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Container-title:Russian Journal of Bioorganic Chemistry
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language:en
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Short-container-title:Russ J Bioorg Chem
Author:
Xie Zhi,Wang Chen,Chen Xianfeng,Liang Yanping,Lan Lizhen,Hong Jiqiong,Qin Jinglin,Li Lili
Abstract
Abstract
Objective: Vitiligo is a systemic dermatological disorder characterized by skin depigmentation due to melanocyte damage and dysfunction. The treatment of vitiligo remains a challenging aspect in dermatological practice. PIWI-interacting RNAs (piRNAs), approximately 24–32 nucleotides in length, are crucial in the epigenetic regulation of developmental processes. However, research on piRNA expression profiling in vitiligo is limited. This study aimed to identify and characterize piRNAs in skin tissues from vitiligo patients and healthy controls. Methods: We compared and analyzed piRNA expression profiles of human vitiligo skin by RNA sequencing. Results and Discussion: Our findings revealed a pronounced preference for uridine (U) at the 5′ end of piRNAs, predominantly originating from repeat and other genomic regions. Notably, we detected 73 differentially expressed piRNAs between the patient and control groups, with 40 piRNAs upregulated and 33 downregulated in vitiligo patients. Bioinformatics analysis indicated that the genes responsible for piRNA production were more prevalent in metabolic processes and implicated in regulating the PI3K-Akt and AMPK signaling pathways. Conclusions: The elucidation of piRNA expression profiles enhances our understanding of their functional roles in the pathogenesis of vitiligo.
Publisher
Pleiades Publishing Ltd
Reference20 articles.
1. Frisoli, M.L., Essien, K., and Harris, J.E., Ann. Rev. Immunology, 2020, vol. 38, pp. 621–648. https://doi.org/10.1146/annurev-immunol-100919023531 2. Bergqvist, C. and Ezzedine, K., Dermatol. (Basel, Switzerland), 2020, vol. 236, pp. 571–592. https://doi.org/10.1159/000506103 3. Iwasaki, Y.W., Siomi, M.C., and Siomi, H., Ann. Rev. Biochem., 2015, vol. 84, pp. 405–433. https://doi.org/10.1146/annurev-biochem-060614034258 4. Chen, S., Ben, S., Xin, J., Li, S., Zheng, R., Wang, H.,Fan, L., Du, M., Zhang, Z., and Wang, M., J. Hematol.Oncol., 2021, vol. 14, p. 93. https://doi.org/10.1186/s13045-021-01104-3 5. Huang, X., Fejes Tóth, K., and Aravin, A.A., Trend. Genet.:TIG, 2017, vol. 33, pp. 882–894. https://doi.org/10.1016/j.tig.2017.09.002
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