Severe acute respiratory syndrome coronavirus protein 7a interacts with hSGT

Biochem Biophys Res Commun. 2006 May 19;343(4):1201-8. doi: 10.1016/j.bbrc.2006.03.091. Epub 2006 Mar 24.

Abstract

Severe acute respiratory syndrome coronavirus (SARS-CoV) 7a is an accessory protein with no known homologues. In this study, we report the interaction of a SARS-CoV 7a and small glutamine-rich tetratricopeptide repeat-containing protein (SGT). SARS-CoV 7a and human SGT interaction was identified using a two-hybrid system screen and confirmed with interaction screens in cell culture and cellular co-localization studies. The SGT domain of interaction was mapped by deletion mutant analysis and results indicated that tetratricopeptide repeat 2 (aa 125-158) was essential for interaction. We also showed that 7a interacted with SARS-CoV structural proteins M (membrane) and E (envelope), which have been shown to be essential for virus-like particle formation. Taken together, our results coupled with data from studies of the interaction between SGT and HIV-1 vpu indicated that SGT could be involved in the life-cycle, possibly assembly of SARS-CoV.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Chlorocebus aethiops
  • Humans
  • Membrane Proteins / metabolism*
  • Molecular Chaperones
  • Molecular Sequence Data
  • Mutation
  • Protein Binding
  • Severe acute respiratory syndrome-related coronavirus*
  • Two-Hybrid System Techniques
  • Vero Cells
  • Viral Envelope Proteins / metabolism*
  • Viral Matrix Proteins / metabolism*
  • Viral Proteins / metabolism*
  • Viral Structural Proteins / metabolism*

Substances

  • Carrier Proteins
  • Membrane Proteins
  • Molecular Chaperones
  • SGTA protein, human
  • Viral Envelope Proteins
  • Viral Matrix Proteins
  • Viral Proteins
  • Viral Structural Proteins
  • sars7a protein, SARS virus

Associated data

  • GENBANK/AY847013