The amino-terminal region of the retinoblastoma gene product binds a novel nuclear matrix protein that co-localizes to centers for RNA processing

J Cell Biol. 1994 Nov;127(3):609-22. doi: 10.1083/jcb.127.3.609.

Abstract

The tumor suppressing capacity of the retinoblastoma protein (p110RB) is dependent on interactions made with cellular proteins through its carboxy-terminal domains. How the p110RB amino-terminal region contributes to this activity is unclear, though evidence now indicates it is important for both growth suppression and regulation of the full-length protein. We have used the yeast two-hybrid system to screen for cellular proteins which bind to the first 300 amino acids of p110RB. The only gene isolated from this screen encodes a novel 84-kD nuclear matrix protein that localizes to subnuclear regions associated with RNA processing. This protein, p84, requires a structurally defined domain in the amino terminus of p110RB for binding. Furthermore, both in vivo and in vitro experiments demonstrate that p84 binds preferentially to the functionally active, hypophosphorylated form of p110RB. Thus, the amino terminus of p110RB may function in part to facilitate the binding of growth promoting factors at subnuclear regions actively involved in RNA metabolism.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Antibodies, Monoclonal
  • Antigens, Nuclear
  • Autoantigens / metabolism
  • Base Sequence
  • Binding Sites
  • Blotting, Western
  • Cell Line
  • Chlorocebus aethiops
  • Cloning, Molecular
  • Escherichia coli
  • Gene Library
  • Genes, Retinoblastoma*
  • Mice
  • Mice, Inbred BALB C / immunology
  • Molecular Sequence Data
  • Molecular Weight
  • Nuclear Matrix / metabolism*
  • Nuclear Proteins / analysis
  • Nuclear Proteins / biosynthesis
  • Nuclear Proteins / metabolism*
  • RNA / metabolism
  • RNA Processing, Post-Transcriptional*
  • Recombinant Fusion Proteins / analysis
  • Recombinant Fusion Proteins / metabolism
  • Restriction Mapping
  • Retinoblastoma Protein / chemistry
  • Retinoblastoma Protein / metabolism*
  • Saccharomyces cerevisiae

Substances

  • Antibodies, Monoclonal
  • Antigens, Nuclear
  • Autoantigens
  • Nuclear Proteins
  • Recombinant Fusion Proteins
  • Retinoblastoma Protein
  • RNA

Associated data

  • GENBANK/L36529