The vibrator Mutation Causes Neurodegeneration via Reduced Expression of PITPα: Positional Complementation Cloning and Extragenic Suppression

Neuron - Tập 18 - Trang 711 - 1997
Roderick T Bronson1, Trevor L Hawkins2, Leonid Kruglyak3, Mary Pat Reeve2, Jennifer L Nemhauser3, Bruce A Hamilton3, Eric S Lander3,2, Edward M Rubin4, Anne W Kerrebrock3, Kenneth L Mueller3, Mark J Daly3, Victor van Berkel3, Desmond J Smith4
1Tufts University Schools of Medicine, Veterinary Medicine, Boston, Massachusetts 02111, and the Jackson Laboratory, 600 Main Street, Bar Harbor, Maine 04609, USA
2Department of Biology Massachusetts Institute of Technology Cambridge, Massachusetts 02139 USA
3Whitehead Institute for Biomedical Research, 9 Cambridge Center, Cambridge, Massachusetts 02142, USA
4Human Genome Center, Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, California 94720, USA

Tóm tắt

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.

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