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Characterization and immune function of the interferon-β promoter stimulator-1 in the barbel chub, Squaliobarbus curriculus.

Abstract
To elucidate the immunity-protecting role of the interferon-β promoter stimulator-1 (ScIPS-1) in barbel chub Squaliobarbus curriculus, the full-length cDNA of ScIPS-1 was cloned and expression levels in response to stimulation were investigated. In addition, the function of ScIPS-1 and its domains were analyzed. The full-length cDNA of ScIPS-1 is 2524 bp and encodes 601 aa. The N-terminal caspase activation and recruitment domain, central proline-rich domain, C-terminal transmembrane domain, C2HC-zinc finger, and Cwf21 domains were identified. The mRNA level of ScIPS-1 was the highest in the kidney, whereas the highest protein level was observed in the liver. The ScIPS-1 expressions were significantly up-regulated after lipopolysaccharide and poly I:C treatment. The ScIPS-1 protein level was up-regulated at 12 h in the head kidney and was up-regulated at 12 h and then down-regulated from 12 to 48 h in the liver after grass carp reovirus (GCRV) infection. The CiIFN and CiMx transcription levels were significantly enhanced in pEGFP-C1-IPS-1 and pcDNA3.1-ΔCwf21 overexpressing cells after GCRV infection. The results indicate that ScIPS-1 may function in the immune response against pathogens and provide a basis for achieving resistance to diseases in fish breeding.
AuthorsXin Zhao, Tiaoyi Xiao, Shengzhen Jin, Jing'an Wang, Junya Wang, Hong Luo, Rui Li, Tong Sun, Jun Zou, Yaoguo Li
JournalDevelopmental and comparative immunology (Dev Comp Immunol) Vol. 104 Pg. 103571 (03 2020) ISSN: 1879-0089 [Electronic] United States
PMID31837379 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2019 Elsevier Ltd. All rights reserved.
Chemical References
  • Adaptor Proteins, Signal Transducing
  • Fish Proteins
  • Lipopolysaccharides
  • MAVS protein, human
  • Interferon-beta
Topics
  • Adaptor Proteins, Signal Transducing (genetics, metabolism)
  • Animals
  • Cells, Cultured
  • Cloning, Molecular
  • Cyprinidae (immunology)
  • Fish Proteins (genetics, metabolism)
  • Head Kidney (immunology, metabolism)
  • Humans
  • Immunity, Innate
  • Interferon-beta (genetics)
  • Lipopolysaccharides (immunology)
  • Reoviridae (physiology)
  • Reoviridae Infections (immunology)
  • Sequence Alignment
  • Up-Regulation

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