Molecular Cloning and Functional Characterization of Mouse Innate Immune Sensor RIG-I
- Authors: Tangjie Zhang 1, Sarkar S.N.2, Zhu J.1,2
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Affiliations:
- College Veterinary Medicine, Yangzhou University
- School of Medicine, University of Pittsburgh
- Issue: Vol 53, No 4 (2019)
- Pages: 325-329
- Section: Article
- URL: https://journal-vniispk.ru/0095-4527/article/view/174115
- DOI: https://doi.org/10.3103/S0095452719040121
- ID: 174115
Cite item
Abstract
Innate immunity functions as the first line against infection, which is mediated by series of innate immune receptors. RIG-I like receptors (RLR) recognize the cytosolic nucleic acids mainly from viruses, trigger the type I interferon (IFN) production, and thus play essential roles in the anti-viral immunity. Here we cloned the mouse RIG-I (mRIG-I) cDNA into the pENTR vector using the TOPO cloning technology, and transferred the FLAG tagged mRIG-I gene from pENTR vector to destination pLenti viral vector. The expression of mRIG-I in transfected cells was detected by immunoblotting using anti-FLAG and anti-RIG-I antibodies. The transfected mRIG-I was active capable of inducing downstream IFN stimulated gene (ISG) gene transcription as well as protein expression.
Keywords
About the authors
Tangjie Zhang
College Veterinary Medicine, Yangzhou University
Author for correspondence.
Email: slx@yzu.edu.cn
China, Yangzhou, 225009
Saumendra N. Sarkar
School of Medicine, University of Pittsburgh
Email: slx@yzu.edu.cn
United States, Pittsburgh, 15232
Jianzhong Zhu
College Veterinary Medicine, Yangzhou University; School of Medicine, University of Pittsburgh
Email: slx@yzu.edu.cn
China, Yangzhou, 225009; Pittsburgh, 15232
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