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The vibrator mutation causes neurodegeneration via reduced expression of PITPα: Positional complementation cloning and extragenic suppression

  • Bruce A. Hamilton
  • , Desmond J. Smith
  • , Kenneth L. Mueller
  • , Anne W. Kerrebrock
  • , Roderick T. Bronson
  • , Victor Van Berkel
  • , Mark J. Daly
  • , Leonid Kruglyak
  • , Mary Pat Reeve
  • , Jennifer L. Nemhauser
  • , Trevor L. Hawkins
  • , Edward M. Rubin
  • , Eric S. Lander

Research output: Contribution to journalArticlepeer-review

181 Scopus citations

Abstract

The mouse vibrator mutation causes an early-onset progressive action tremor, degeneration of brain stem and spinal cord neurons, and juvenile death. We cloned the vibrator mutation using an in vivo positional complementation approach and complete resequencing of the resulting 76 kb critical region from vibrator and its parental chromosome. The mutation is an intracisternal A particle retroposon insertion in intron 4 of the phosphatidylinositol transfer protein α gene, causing a 5-fold reduction in RNA and protein levels. Expression of neurofilament light chain is also reduced in vibrator, suggesting one signaling pathway that may underlie vibrator pathology. The vibrator phenotype is suppressed in one intercross. We performed a complete genome scan and mapped a major suppressor locus (Mvb- 1) to proximal chromosome 19.

Original languageEnglish
Pages (from-to)711-722
Number of pages12
JournalNeuron
Volume18
Issue number5
DOIs
StatePublished - May 1997
Externally publishedYes

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