期刊
CELL
卷 144, 期 1, 页码 106-118出版社
CELL PRESS
DOI: 10.1016/j.cell.2010.11.053
关键词
-
资金
- National Institutes of Health through National Institute of Neurological Disorders and Stroke [R37NS037116]
- Howard Hughes Medical Institute
- NINDS [R37NS037116, P01NS031249]
The Alzheimer's disease-linked gene presenilin is required for intramembrane proteolysis of amyloid-beta precursor protein, contributing to the pathogenesis of neurodegeneration that is characterized by loss of neuronal connections, but the role of Presenilin in establishing neuronal connections is less clear. Through a forward genetic screen in mice for recessive genes affecting motor neurons, we identified the Columbus allele, which disrupts motor axon projections from the spinal cord. We mapped this mutation to the Presenilin-1 gene. Motor neurons and commissural interneurons in Columbus mutants lacking Presenilin-1 acquire an inappropriate attraction to Netrin produced by the floor plate because of an accumulation of DCC receptor fragments within the membrane that are insensitive to Slit/Robo silencing. Our findings reveal that Presenilin-dependent DCC receptor processing coordinates the interplay between Netrin/DCC and Slit/Robo signaling. Thus, Presenilin is a key neural circuit builder that gates the spatiotemporal pattern of guidance signaling, thereby ensuring neural projections occur with high fidelity.
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