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Systematic identification of chicken type I, II and III interferon-stimulated genes

Authors
  • Dai, Manman1
  • Xie, Tingting1, 2
  • Liao, Ming1
  • Zhang, Xiquan1, 2
  • Feng, Min1
  • 1 South China Agricultural University, Guangzhou, China , Guangzhou (China)
  • 2 Ministry of Agriculture, Guangzhou, Guangdong, China , Guangzhou (China)
Type
Published Article
Journal
Veterinary Research
Publisher
BioMed Central
Publication Date
May 24, 2020
Volume
51
Issue
1
Identifiers
DOI: 10.1186/s13567-020-00793-x
Source
Springer Nature
License
Green

Abstract

Interferon-stimulated genes (ISGs) play an important role in antiviral innate immune responses. Although many ISGs have been identified in mammals, researchers commonly recognize that many more ISGs are yet to be discovered. Current information is still very limited particularly for the systematic identification of type III ISGs. Similarly, current research on ISGs in birds is still in its infancy. The aim of this study was to systematically identify chicken type I (IFN-α), II (IFN-γ) and III (IFN-λ) ISGs and analyze their respective response elements. RNA sequencing (RNA-Seq) was employed to identify those genes with up-regulated expression following chicken IFN-α, IFN-γ and IFN-λ treatment. Two hundred and five type I ISGs, 299 type II ISGs, and 421 type III ISGs were identified in the chicken. We further searched for IFN-stimulated response elements (ISRE) and gamma-activated sequences (GAS) elements in the promoters region of ISGs. The GAS elements were common in the promoter of type II ISGs and were even detected in type I and III ISGs. However, ISRE were not commonly found in the promoters of chicken ISGs. Furthermore, we demonstrated that ISRE in chicken cells were significantly activated by IFN-α or IFN-λ treatment, and expectedly, that GAS elements were also significantly activated by IFN-γ treatment. Interestingly, we also found that GAS elements were significantly activated by IFN-λ. Our study provides a systematic library of ISGs in the chicken together with preliminary information about the transcriptional regulation of the identified ISGs.

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