4.7 Article

Screening of genes encoding proteins that interact with ISG15: Probing a cDNA library from a snakehead fish cell line using a yeast two-hybrid system

Journal

FISH & SHELLFISH IMMUNOLOGY
Volume 128, Issue -, Pages 300-306

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.fsi.2022.07.070

Keywords

ISG 15; cDNA library; Snakehead fish cell line; Yeast two -hybrid system

Funding

  1. National Natural Science Foundation of China [32002420]
  2. Natural Science Foundation of Jiangsu Province [BK20190916]
  3. Jiangsu Agriculture Science and Technology Innovation Found [CX(21)3162]
  4. China postdoctoral Science Foundation [2021M702761]
  5. 'Blue Project' of Yangzhou University

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This study investigates the interaction between snakehead ISG15 and other proteins using a yeast expression system, and identifies multiple interacting proteins. These results are important for further exploration of the function and mechanism of snakehead ISG15.
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 x 109 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 inter-action 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.

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