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ZIRC
ZFIN ID: ZDB-PUB-150422-9
Cloning, identification of the two cytokine receptor family B subunits CRFB1 and CRFB5 from grass carp (Ctenopharyngodon idella)
Chen, H., Liu, W., Wang, B., Mao, H., Sun, Z., Hou, Q., Mi, Y., Fan, L., Hu, C.
Date: 2015
Source: Fish & shellfish immunology 45(2): 211-20 (Journal)
Registered Authors:
Keywords: Antiviral signaling pathway, CRFB1 and CRFB5, Cytokine receptor family B, Teleost, Type I interferon
MeSH Terms:
  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Carps/genetics*
  • Carps/metabolism
  • Cloning, Molecular
  • DNA, Complementary/genetics
  • DNA, Complementary/metabolism
  • Fish Proteins/genetics*
  • Fish Proteins/metabolism
  • Molecular Sequence Data
  • Phylogeny
  • Protein Subunits/genetics
  • Protein Subunits/metabolism
  • RNA, Messenger/genetics
  • RNA, Messenger/metabolism
  • Real-Time Polymerase Chain Reaction/veterinary
  • Receptors, Interferon/genetics*
  • Receptors, Interferon/metabolism
  • Signal Transduction*
PubMed: 25891274 Full text @ Fish Shellfish Immunol.
ABSTRACT
Similar to the mammalian counterparts, fish type I interferon (IFN) performs its potential biological activities via binding to the corresponding receptor on target cell membrane. Fish type I IFN receptor, a kind of enzyme-linked receptor, consists of two subunits and belongs to the class II cytokine receptor family B (CRFB). In the present study, we cloned and identified two putative grass carp (Ctenopharyngodon idella) type I interferon receptor subunits (termed CiCRFB1 and CiCRFB5) by homology cloning techniques. Phylogenetic tree analysis suggested that CiCRFB1 and CiCRFB5 shared highly homology to Danio rerio CRFB1 and CRFB5 respectively. CiCRFB1 and CiCRFB5 were up-regulated after the stimulation with Grass Carp Hemorrhagic Virus (GCHV) and Polyinosinic-polycytidylic acid (Poly I:C), indicating that they are related to the intracellular antiviral activity. In order to know more about the roles of CiCRFB1 and CiCRFB5 in the process, the extracellular domains of CiCRFB1 (CiCRFB1-EC) and CiCRFB5 (CiCRFB5-EC), as well as grass carp type I IFN (CiIFN) were expressed in Escherichia coli BL21, and purified by affinity chromatography with the Ni-NTA His-Bind resin. Cross-linking reactions were employed to analyze the affinity of the ligand (CiIFN) with the two putative receptor subunits (CiCRFB1-EC and CiCRFB5-EC). The result suggested the formation of (CiCRFB5)2 homodimer was more easily than that of (CiCRFB1)2 under the induction of CiIFN in vitro. However, CiIFN was inclined to bind to (CiCRFB1)2 homodimer. Interestingly, although CiIFN seemed unable to facilitate the formation of (CiCRFB1 + CiCRFB5) heterodimer in the absence of DSS cross linker, however it can bind to the heterodimer in the presence of DSS. This indicated that the homodimer and the heterodimer were the potential receptor for CiIFN.
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