Spinal muscular atrophy (SMA) is the most common inherited cause of death in infants and young children. SMA is caused by the deletion or mutation in the survival of motor neuron 1 (SMN1) gene, leading to a deficiency of the ubiquitously expressed SMN protein. Currently, there is no effective treatment option available for SMA. Evidence from studies in humans and rodents suggests that increasing SMN protein levels in the central nervous system is sufficient to ameliorate the disease phenotype and prolong survival. To identify protective modifiers of SMN protein levels we performed a genome-wide RNAi screen. Genes we identified in this screen will allow us to investigate genetic modifiers and molecular pathways that regulate SMN protein levels. These targets and pathways should provide novel avenues for therapeutic development for the treatment of SMA.

Public Health Relevance

Spinal muscular atrophy (SMA) is a motor neuron disease and one of the leading inherited causes of infant mortality, affecting about 1 in 8000 live births. The disease is caused by deficiency of the survival motor neuron (SMN) protein and there is currently no effective treatment. The studies outlined in this proposal will identify genetic modifiers of SMN protein levels and define the molecular mechanisms regulating SMN protein stability in order to find new therapeutic targets for treating SMA.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS091575-03
Application #
9405053
Study Section
Cellular and Molecular Biology of Neurodegeneration Study Section (CMND)
Program Officer
Nuckolls, Glen H
Project Start
2016-04-01
Project End
2020-12-31
Budget Start
2018-01-01
Budget End
2018-12-31
Support Year
3
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Henry M. Jackson Fdn for the Adv Mil/Med
Department
Type
DUNS #
144676566
City
Bethesda
State
MD
Country
United States
Zip Code
20817