Decreased gene expression of calretinin and ryanodine receptor type 1 in tottering mice

Brain Res Bull. 2002 Oct 15;59(1):53-8. doi: 10.1016/s0361-9230(02)00841-9.

Abstract

Tottering mice are a spontaneously occurring animal model of human absence epilepsy. They carry a mutation in the P/Q-type calcium channel alpha1A subunit gene which is highly expressed by cerebellar Purkinje cells. In this study, we investigated the role of calretinin and ryanodine receptor type 1 (RyR1) gene expression in the cerebellum of tottering mice. Cerebellar tissue specimens from four experimental groups were processed for in situ hybridization histochemistry (ISHH): (1) wild-type (+/+); (2) heterozygous (tg/+) and two homozygous groups; either (3) without occurrence of an episode of paroxysmal dyskinesia (tg/tg-N); or (4) after an episode of paroxysmal dyskinesia (tg/tg-P) that lasted about 45 min on average. Quantitative analysis showed a statistically significant decrease (p = 0.0001, ANOVA) of calretinin gene expression at the level of the simple lobule of the cerebellum in both homozygous groups compared to the wild-type and heterozygous groups. RyR1 was decreased in the flocculus of the cerebellum in both the tg/tg-N and tg/tg-P groups compared to wild type (p = 0.0174, ANOVA). These results suggest that calretinin gene expression, as well as other genes involved in regulation of calcium homeostasis, such as RyR1, may play a role in the biochemical functional alterations present in tottering mice.

MeSH terms

  • Animals
  • Calbindin 2
  • Calcium / metabolism
  • Calcium Channels, P-Type / deficiency
  • Calcium Channels, P-Type / genetics
  • Calcium Signaling / genetics*
  • Cerebellum / metabolism*
  • Cerebellum / physiopathology
  • Chorea / genetics*
  • Chorea / metabolism
  • Chorea / physiopathology
  • Disease Models, Animal
  • Down-Regulation / genetics
  • Epilepsy, Absence / genetics*
  • Epilepsy, Absence / metabolism
  • Epilepsy, Absence / physiopathology
  • Female
  • Gene Expression Regulation / physiology*
  • Homeostasis / genetics
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Neurologic Mutants
  • Mutation / genetics
  • Purkinje Cells / metabolism
  • RNA, Messenger / metabolism
  • Ryanodine Receptor Calcium Release Channel / genetics
  • Ryanodine Receptor Calcium Release Channel / metabolism*
  • S100 Calcium Binding Protein G / genetics
  • S100 Calcium Binding Protein G / metabolism*

Substances

  • CALB2 protein, human
  • Calb2 protein, mouse
  • Calbindin 2
  • Calcium Channels, P-Type
  • RNA, Messenger
  • Ryanodine Receptor Calcium Release Channel
  • S100 Calcium Binding Protein G
  • Calcium