Molecular characterization and functional analysis of duck CCCH-type zinc finger antiviral protein (ZAP)

• Published in: Biochemical and biophysical research communications 2021-07, Vol.561, p.52-58
• Main Authors: Zhang, Rongrong, He, Yan, Zhu, Xinyu, Wen, Guoyuan, Luo, Qingping, Zhang, Tengfei, Lu, Qin, Liu, Shudan, Xiao, Shaobo, Fang, Liurong, Shao, Huabin
• Format: Article
• Language: English
• Subjects: DTMUV; Duck; Interferon-β; ZAP
• ISSN: 0006-291X; 1090-2104
• DOI: 10.1016/j.bbrc.2021.05.019

This is the first study to clone duck CCCH-type zinc finger antiviral protein (duZAP) from Jingjiang duck (Anas platyrhynchos). Full-length duZAP cDNA was 2154 bp and encoded a 717-amino acid polypeptide containing four highly conserved CCCH-type finger motifs, a WWE domain and a poly (ADP-ribose) polymerase (PARP) domain. duZAP was expressed in multiple duck tissues, with the highest mRNA expression in the spleen. Overexpression of duZAP in duck embryo fibroblast cells (DEFs) led to activation of the transcription factors IRF1 and NF-κB, and induction of IFN-β. Analysis of deletion mutants revealed that both the WWE and PARP domains of duZAP were essential for activating the IFN-β promoter. Knockdown of duZAP in DEFs significantly reduced poly (I:C)- and duck Tembusu virus (DTMUV)-induced IFN-β activation. Our findings further the understanding of the role of duZAP in the duck innate immune response. •DuZAP is expressed in various tissues of ducklings.•DuZAP activated IRF1 and NF-κB, as well as induced IFN-β expression.•The WWE and PARP domains of duZAP are essential for IFN-β promoter activation.