Grass carp (Ctenopharyngodon idella) TNK1 modulates JAK-STAT signaling through phosphorylating STAT1

Dev Comp Immunol. 2021 Mar:116:103951. doi: 10.1016/j.dci.2020.103951. Epub 2020 Nov 27.

Abstract

TNK1 (thirty-eight-negative kinase 1) belongs to the ACK (Activated Cdc42 Kinases) family of intracellular non-receptor tyrosine kinases that usually acts as an important regulator in cytokine receptor-mediated intracellular signal transduction pathways. JAK-STAT signal pathway acts as a key point in cellular proliferation, differentiation and immunomodulatory. Mammalian TNK1 is involved in antiviral immunity and activation of growth factors. However, TNK1 has rarely been studied in fish. To evaluate the role of fish TNK1 in JAK-STAT pathway, we cloned the full-length cDNA sequence of grass carp (Ctenopharyngodon idella) TNK1 (CiTNK1). CiTNK1 protein consists of N-terminal Tyrkc (tyrosine kinase) domain, C-terminal SH3 (Src homology 3) domain and Pro-rich domain. Phylogenetic analysis showed that CiTNK1 has a closer relationship with Danio rerio TNK1. The expression and phosphorylation of CiTNK1 in grass carp tissues and cells was increased under poly(I:C) stimulation. Subcellular localization and co-immunoprecipitation indicated that CiTNK1 is targeted in the cytoplasm and interacts with grass carp STAT1 (CiSTAT1). Co-transfection of CiTNK1 and CiSTAT1 into cells facilitated the expression of IFN I. This is because that the presence of CiTNK1 enhanced the phosphorylation of CiSTAT1 and causes activation of CiSTAT1. Our results revealed that TNK1 can potentiate the phosphorylation of STAT1 and then regulates JAK-STAT pathway to trigger IFN I expression in fish.

Keywords: Fish; IFN I; JAK-STAT; Phosphorylation; TNK1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Carps / metabolism*
  • Cytoplasm / metabolism
  • Fish Proteins / genetics
  • Fish Proteins / metabolism
  • Gene Expression
  • Interferon Type I / genetics
  • Interferon Type I / metabolism
  • Janus Kinases / metabolism*
  • Phosphorylation
  • Phylogeny
  • Poly I-C / metabolism
  • Protein Binding
  • Protein-Tyrosine Kinases / genetics
  • Protein-Tyrosine Kinases / metabolism*
  • STAT1 Transcription Factor / metabolism*
  • Sequence Alignment
  • Signal Transduction

Substances

  • Fish Proteins
  • Interferon Type I
  • STAT1 Transcription Factor
  • Protein-Tyrosine Kinases
  • Janus Kinases
  • Poly I-C