In vivo viability of postmitotic Purkinje neurons requires pRb family member function

Mol Cell Neurosci. 1995 Apr;6(2):153-67. doi: 10.1006/mcne.1995.1014.

Abstract

The product of the retinoblastoma susceptibility gene, pRb, is known to be an important regulator of cell division. Disrupted central nervous system development in RB null mice suggests a critical function for pRb in the proliferative arrest and initiation of terminal differentiation of certain neurons. Previously, we have shown that SV40 T-ag expression targeted to Purkinje neurons in transgenic mice causes cell-specific death. Here we describe that T-ag expression induces DNA synthesis and results in DNA fragmentation in Purkinje neurons. Characterization of transgenic mouse lines expressing mutant T-ags demonstrate that the pRb binding domain of T-ag is required for induction of Purkinje cell loss. These findings indicate that a pRb function is required well beyond the completion of Purkinje neuron differentiation and provide a link between cell cycle regulation and neurodegeneration in vivo.

Publication types

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

MeSH terms

  • Animals
  • Antigens, Polyomavirus Transforming / genetics
  • Apoptosis / genetics
  • Base Sequence
  • Blotting, Northern
  • Cell Cycle / genetics
  • Cell Division / physiology
  • Cell Survival / genetics
  • Cerebellum / pathology
  • DNA / biosynthesis
  • DNA Damage
  • Genes, Retinoblastoma / physiology*
  • Immunohistochemistry
  • Mice
  • Mice, Transgenic
  • Molecular Sequence Data
  • Purkinje Cells / cytology
  • Purkinje Cells / physiology*

Substances

  • Antigens, Polyomavirus Transforming
  • DNA