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

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.

Pubmed ID: 7525595 RIS Download

Mesh terms: Amino Acid Sequence | Animals | Antibodies, Monoclonal | Antigens, Nuclear | Autoantigens | Base Sequence | Binding Sites | Blotting, Western | Cell Line | Cercopithecus aethiops | Cloning, Molecular | Escherichia coli | Gene Library | Genes, Retinoblastoma | Mice | Mice, Inbred BALB C | Molecular Sequence Data | Molecular Weight | Nuclear Matrix | Nuclear Proteins | RNA | RNA Processing, Post-Transcriptional | Recombinant Fusion Proteins | Restriction Mapping | Retinoblastoma Protein | Saccharomyces cerevisiae

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