PUBLICATION

Molecular characterisation and inductive expression of a fish protein arginine methyltransferase 1 gene in response to virus infection

Authors
Dong, C.W., Zhang, Y.B., Lu, A.J., Zhu, R., Zhang, F.T., Zhang, Q.Y., and Gui, J.F.
ID
ZDB-PUB-061031-3
Date
2007
Source
Fish & shellfish immunology   22(4): 380-393 (Journal)
Registered Authors
Keywords
Protein arginine methyltransferase 1, Paralichthys olivaceus, Scophthalmus maximus rhabdovirus virus (SMRV), Virus infection, Differential expression, Antiviral immune response
MeSH Terms
  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Cell Line
  • DNA Primers/chemistry
  • Embryo, Nonmammalian/cytology
  • Fish Diseases/enzymology
  • Fish Diseases/immunology*
  • Fish Diseases/virology
  • Flounder/genetics
  • Flounder/immunology*
  • Flounder/virology
  • Gene Expression Regulation, Enzymologic/immunology*
  • Molecular Sequence Data
  • Phylogeny
  • Protein-Arginine N-Methyltransferases/biosynthesis
  • Protein-Arginine N-Methyltransferases/chemistry
  • Protein-Arginine N-Methyltransferases/genetics*
  • Protein-Arginine N-Methyltransferases/immunology
  • RNA, Messenger
  • Reverse Transcriptase Polymerase Chain Reaction/veterinary
  • Rhabdoviridae/immunology
  • Rhabdoviridae Infections/enzymology
  • Rhabdoviridae Infections/immunology
  • Rhabdoviridae Infections/veterinary*
  • Sequence Alignment/veterinary
  • Sequence Homology, Amino Acid
  • Up-Regulation
PubMed
17055744 Full text @ Fish Shellfish Immunol.
Abstract
Protein arginine methyltransferase 1 (PRMT1) is currently thought as an effector to regulate interferon (IFN) signalling. Here Paralichthys olivaceus PRMT1 (PoPRMT1) gene was identified as a virally induced gene from UV-inactivated Scophthalmus maximus Rhabdovirus (SMRV)-infected flounder embryonic cells (FEC). PoPMRT1 encodes a 341-amino-acid protein that shares the conserved domains including post-I, motif I, II and III. Homology comparisons show that the putative PoPMRT1 protein is the closest to zebrafish PMRT1 and belongs to type I PRMT family (including PRMT1, PRMT2, PRMT3, PRMT4, PRMT6, PRMT8). Expression analyses revealed an extensive distribution of PoPMRT1 in all tested tissues of flounder. In vitro induction of PoPRMT1 was determined in UV-inactivated SMRV-infected FEC cells, and under the same conditions, flounder Mx was also transcriptionally up-regulated, indicating that an IFN response might be triggered. Additionally, live SMRV infection of flounders induced an increased expression of PoPRMT1 mRNA and protein significantly in spleen, and to a lesser extent in head kidney and intestine. Immunofluorescence analysis revealed a major cyptoplasmic distribution of PoPRMT1 in normal FEC but an obvious increase occurred in nucleus in response to UV-inactivated SMRV. This is the first report on in vitro and in vivo expression of fish PRMT1 by virus infection, suggesting that PoPRMT1 might be implicated in flounder antiviral immune response.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping