College of Animal Science and Technology, Yangzhou University, Yangzhou, 225009, China.
College of Animal Science and Technology, Yangzhou University, Yangzhou, 225009, China.
Fish Shellfish Immunol. 2022 Sep;128:300-306. doi: 10.1016/j.fsi.2022.07.070. Epub 2022 Jul 31.
Interferon-stimulated gene 15 (ISG15) regulates cellular life processes, including defense responses against infection by a variety of viral pathogens, by binding to target proteins. At present, various fish ISG15s have been identified, but the biological function of ISG15 in snakehead fish is still unclear. In this study, total RNA was extracted from snakehead fish cell line E11, ds cDNA was synthesized and purified using SMART technology, and the resulting cDNA library was screened by co-transforming yeast cells. The library titer was 4.28 × 10 CFU/mL. Using snakehead ISG15 as the bait protein, the recombinant bait vector pGBKT7-ISG15 was constructed and transformed into the yeast strain Y2HGold. The toxicity and self-activation activity of the bait vector were detected on the deficient medium, and the prey proteins interacting with ISG15 were screened. In total, 19 interacting proteins of ISG15 were identified, including mitotic checkpoint protein BUB3, hypothetical protein SnRVgp6, elongation factor 1-beta, 60S ribosomal protein L9, dual specificity protein phosphatase 5-like, eukaryotic translation initiation factor 3 subunit I and ferritin. A yeast spotting assay further probed the interaction between ISG15 and DUSP5. These results increase our understanding of the interaction network of snakehead ISG15 and will aid in exploring the underlying mechanisms of snakehead ISG15 functions in the future.
干扰素刺激基因 15(ISG15)通过与靶蛋白结合,调节细胞的生命过程,包括抵抗各种病毒病原体感染的防御反应。目前已经鉴定出多种鱼类的 ISG15,但 ISG15 在乌鳢中的生物学功能尚不清楚。本研究从乌鳢细胞系 E11 中提取总 RNA,采用 SMART 技术合成并纯化 ds cDNA,然后将其 cDNA 文库转化酵母细胞进行筛选。文库滴度为 4.28×10 CFU/mL。用乌鳢 ISG15 作为诱饵蛋白,构建了重组诱饵载体 pGBKT7-ISG15,并将其转化到酵母菌株 Y2HGold 中。在缺陷培养基上检测诱饵载体的毒性和自激活活性,并筛选与 ISG15 相互作用的猎物蛋白。共鉴定到 19 个与 ISG15 相互作用的蛋白,包括有丝分裂检查点蛋白 BUB3、假定蛋白 SnRVgp6、延伸因子 1-β、60S 核糖体蛋白 L9、双特异性蛋白磷酸酶 5 样、真核翻译起始因子 3 亚基 I 和铁蛋白。酵母点杂交实验进一步证实了 ISG15 与 DUSP5 之间的相互作用。这些结果增加了我们对乌鳢 ISG15 相互作用网络的认识,并有助于未来探索乌鳢 ISG15 功能的潜在机制。