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 language | English |
|---|---|
| Pages (from-to) | 711-722 |
| Number of pages | 12 |
| Journal | Neuron |
| Volume | 18 |
| Issue number | 5 |
| DOIs | |
| State | Published - May 1997 |
| Externally published | Yes |
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