A nuclear protein derived from brain cells stimulates transcription of the human neurotropic virus promoter, JCVE, in vitro

J Biol Chem. 1990 Aug 15;265(23):13899-905.

Abstract

The 98-base pair enhancer/promoter sequence is critical for cell type-specific transcription of the human neurotropic viral promoter, JCVE, in glial cells. Transcriptionally active extracts were prepared from glial cells and used to identify cis- and trans-acting regulatory elements that are involved in the glial-specific activation of the JCVE promoter. Results indicate that multiple regulatory sequences within the 98-base pair repeat specifically bind to nuclear proteins present in glial cells and positively regulate viral early RNA synthesis. The central region of the repeat, designated domain-B, interacts with a 45-kDa nuclear protein present in brain cells. This brain-specific protein was purified by conventional and DNA affinity chromatography. Complementation of the highly purified protein with HeLa extract significantly increased JCVE promoter activity. Thus, association of the novel glial-origin transcription factor with its target sequence increases transcription of the JCVE promoter in a non-glial context.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Base Sequence
  • Brain / metabolism*
  • Cattle
  • Enhancer Elements, Genetic
  • HeLa Cells / metabolism
  • Humans
  • JC Virus / genetics*
  • Molecular Sequence Data
  • Neuroglia / metabolism
  • Nuclear Proteins / isolation & purification
  • Nuclear Proteins / metabolism*
  • Oligonucleotide Probes / chemical synthesis
  • Polyomavirus / genetics*
  • Promoter Regions, Genetic*
  • Transcription, Genetic*

Substances

  • Nuclear Proteins
  • Oligonucleotide Probes