Identification of DDX1 as a JC virus transcriptional control region-binding protein

Microbiol Immunol. 2007;51(3):327-37. doi: 10.1111/j.1348-0421.2007.tb03915.x.

Abstract

To investigate the mechanism behind JC virus (JCV) cell specificity we performed electrophoretic mobility shift assays (EMSA) using probes derived from the JCV transcriptional control region (JCV-TCR). Using nuclear extracts from the JCV-susceptible neuroblastoma cell line IMR-32, EMSA revealed a 670 kDa JCV-TCR-binding protein complex designated as #3-bp. This complex could not be detected in nuclear extracts from non-susceptible cell lines. Using column chromatographic purifi-cation and microsequencing, we identified cleavage stimulation factor (CstF) as a component of #3-bp. However, as CstF is present in many cell types, we speculated that the IMR-32-specific component(s) of #3-bp bind CstF. We performed a yeast two-hybrid assay using CstF-77 as the bait against a HeLa cDNA-subtracted IMR-32 cDNA library. This analysis detected binding between CstF-77 and the RNA helicase DDX1. Subsequently, biotinylated DNA affinity precipitation and chromatin immunoprecipitation assays also confirmed that DDX1 binds specifically to JCV-TCR. Our findings indicate that an association between DDX1 and the JCV-TCR may play a significant role in JCV infection in IMR-32 cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • Cleavage Stimulation Factor / genetics
  • Cleavage Stimulation Factor / metabolism
  • DEAD-box RNA Helicases / genetics
  • DEAD-box RNA Helicases / metabolism*
  • Electrophoresis, Polyacrylamide Gel
  • HeLa Cells
  • Humans
  • JC Virus / genetics*
  • JC Virus / isolation & purification
  • Neuroblastoma / metabolism
  • Neuroblastoma / virology
  • Polyomavirus Infections / genetics
  • Polyomavirus Infections / metabolism
  • Polyomavirus Infections / virology
  • Protein Binding
  • Tumor Virus Infections / genetics
  • Tumor Virus Infections / metabolism
  • Tumor Virus Infections / virology

Substances

  • Cleavage Stimulation Factor
  • DDX1 protein, human
  • DEAD-box RNA Helicases