Bicaudal D1-dependent trafficking of human cytomegalovirus tegument protein pp150 in virus-infected cells

J Virol. 2010 Apr;84(7):3162-77. doi: 10.1128/JVI.01776-09. Epub 2010 Jan 20.

Abstract

Human cytomegalovirus (HCMV) virion assembly takes place in the nucleus and cytoplasm of infected cells. The HCMV virion tegument protein pp150 (ppUL32) is an essential protein of HCMV and has been suggested to play a role in the cytoplasmic phase of HCMV assembly. To further define its role in viral assembly and to identify host cell proteins that interact with pp150 during viral assembly, we utilized yeast two-hybrid analyses to detect an interaction between pp150 and Bicaudal D1 (BicD1), a protein thought to play a role in trafficking within the secretory pathway. BicD1 is known to interact with the dynein motor complex and the Rab6 GTPase. The interaction between pp150 and BicD1 was confirmed by coimmunoprecipitation and fluorescence resonance energy transfer. Depletion of BicD1 with short hairpin RNA (shRNA) caused decreased virus yield and a defect in trafficking of pp150 to the cytoplasmic viral assembly compartment (AC), without altering trafficking to the AC of another essential tegument protein, pp28, or the viral glycoprotein complex gM/gN. The C terminus of BicD1 has been previously shown to interact with the GTPase Rab6, suggesting a potential role for Rab6-mediated vesicular trafficking in HCMV assembly. Finally, overexpression of the N terminus of truncated BicD1 acts in a dominant-negative manner and leads to disruption of the AC and a decrease in the assembly of infectious virus. This phenotype was similar to that observed following overexpression of dynamitin (p50) and provided additional evidence that morphogenesis of the AC and virus assembly were dynein dependent.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adaptor Proteins, Signal Transducing / analysis
  • Adaptor Proteins, Signal Transducing / chemistry
  • Adaptor Proteins, Signal Transducing / physiology*
  • Animals
  • COS Cells
  • Cells, Cultured
  • Chlorocebus aethiops
  • Cytoskeletal Proteins / analysis
  • Cytoskeletal Proteins / chemistry
  • Cytoskeletal Proteins / physiology*
  • Dyneins / physiology
  • Fluorescence Resonance Energy Transfer
  • Humans
  • Microtubules / physiology
  • Phosphoproteins / analysis
  • Phosphoproteins / metabolism*
  • Protein Structure, Tertiary
  • Protein Transport
  • Two-Hybrid System Techniques
  • Viral Matrix Proteins / analysis
  • Viral Matrix Proteins / metabolism*
  • Virus Assembly

Substances

  • Adaptor Proteins, Signal Transducing
  • BICD1 protein, human
  • Cytoskeletal Proteins
  • Phosphoproteins
  • Viral Matrix Proteins
  • pp150 protein, Cytomegalovirus
  • Dyneins