Cao Trang Thi Thuy, Nguyen Tuan Anh, Nguyen Minh Huy Cong, Ngo Trang Trang Thi Huyen, Dang Thao Thi Phuong
Department of Molecular and Environmental Biotechnology, Faculty of Biology and Biotechnology, University of Science, Ho Chi Minh City, Vietnam.
Department of Molecular and Environmental Biotechnology, Faculty of Biology and Biotechnology, University of Science, Ho Chi Minh City, Vietnam
Life Sci Alliance. 2025 Aug 18;8(11). doi: 10.26508/lsa.202503246. Print 2025 Nov.
Ubiquitin C-terminal hydrolase L1 (UCH-L1) is a protein in the ubiquitin-proteasome system involved in numerous cellular processes and implicated in various human diseases, including cancer, neurodegenerative diseases, and metabolic syndrome. However, its roles in development remain poorly understood. In this study, we used as a model to investigate the function of UCH-L1. The homolog of , , was specifically knocked down in the eye imaginal disk using RNA interference (RNAi). The results showed that loss of Uch function induced a rough eye phenotype characterized by abnormal ommatidia, including disorganized arrangement, variable sizes, and irregular orientations. In addition, Uch knockdown significantly affected cone cells, photoreceptor cells, and pigment cells. Remarkably, these defects were fully rescued when , a protease that releases the Spitz, the ligand of EGFR signaling, was co-knocked down. Taken together, these findings strongly demonstrated that Uch plays a crucial role in the development of various eye cell types and functions in coordination with rhomboid-1 in the EGFR signaling pathway.
泛素羧基末端水解酶L1(UCH-L1)是泛素-蛋白酶体系统中的一种蛋白质,参与众多细胞过程,并与多种人类疾病相关,包括癌症、神经退行性疾病和代谢综合征。然而,其在发育过程中的作用仍知之甚少。在本研究中,我们以[具体生物名称]作为模型来研究UCH-L1的功能。通过RNA干扰(RNAi)技术,在眼成虫盘特异性敲低了[具体生物名称]的同源物Uch。结果表明,Uch功能缺失诱导了粗糙眼表型,其特征为小眼异常,包括排列紊乱、大小不一和方向不规则。此外,Uch敲低显著影响了视锥细胞、感光细胞和色素细胞。值得注意的是,当与rhomboid-1(一种释放表皮生长因子受体(EGFR)信号配体Spitz的蛋白酶)共同敲低时,这些缺陷完全得到挽救。综上所述,这些发现有力地证明了Uch在多种[具体生物名称]眼细胞类型的发育中起关键作用,并在[具体生物名称]的EGFR信号通路中与rhomboid-1协同发挥作用。