Description:
<jats:title>Abstract</jats:title><jats:p>The Purkinje cell (PC) degeneration (<jats:italic>pcd</jats:italic>) phenotype results from mutation in <jats:italic>nna1</jats:italic> gene and is associated with the degeneration and death of PCs during the postnatal life. Although the <jats:italic>pcd</jats:italic> mutation is a model of the ataxic mouse, it shares clinical and pathological characteristics of inherited human spinocerebellar ataxias. PC degeneration in <jats:italic>pcd</jats:italic> mice provides a useful neuronal system to study nuclear mechanisms involved in DNA damage‐dependent neurodegeneration, particularly the contribution of nucleoli and Cajal bodies (CBs). Both nuclear structures are engaged in housekeeping functions for neuronal survival, the biogenesis of ribosomes and the maturation of snRNPs and snoRNPs required for pre‐mRNA and pre‐rRNA processing, respectively. In this study, we use ultrastructural analysis, <jats:italic>in situ</jats:italic> transcription assay and molecular markers for DNA damage, nucleoli and CB components to demonstrate that PC degeneration involves the progressive accumulation of nuclear DNA damage associated with disruption of nucleoli and CBs, disassembly of polyribosomes into monoribosomes, ribophagy and shut down of nucleolar and extranucleolar transcription. Microarray analysis reveals that four genes encoding repressors of nucleolar rRNA synthesis (p53, Rb, PTEN and SNF2) are upregulated in the cerebellum of <jats:italic>pcd</jats:italic> mice. Collectively, these data support that nucleolar and CB alterations are hallmarks of DNA damage‐induced neurodegeneration.</jats:p>