AbstractThe survival motor neuron (SMN) protein forms cytoplasmic granules when overexpressed. We report here that SMN co-localizes with TIA-1/R and G3BP, protein assemblers of stress granules (SGs), and that SMN is co-immunoprecipitated with TIA-1/R, suggesting that SMN granules are SGs. Formation of SMN granules precedes accumulation of TIA-1/R, indicating that SMN serves as a facilitator of SG formation. However, the exon 7 skipping product, SMNΔ7, is largely retained in the nucleus and forms nuclear granules, indicating that exon 7 is critical for SG formation. Our findings reveal a novel SMN function and possible SG involvement in the pathogenesis of spinal muscular atrophy
AbstractBackground: The survival of motor neurons (SMN) protein is the protein product of the spinal...
International audienceSpinal muscular atrophy is a neuromuscular disease resulting from mutations in...
Spinal muscular atrophy is an autosomal recessive genetic disease that results from the loss and/or ...
AbstractThe survival motor neuron (SMN) protein forms cytoplasmic granules when overexpressed. We re...
Survival motor neuron (SMN) is an essential and ubiquitously expressed protein that participates in ...
Survival motor neuron (SMN) is an essential and ubiquitously expressed protein that participates in ...
Survival motor neuron (SMN) is an essential and ubiquitously expressed protein that participates in ...
Childhood spinal muscular atrophy (SMA) is caused by a reduction in survival motor neuron (SMN) prot...
Proximal spinal muscular atrophy (SMA) is a neurodegenerative disorder caused by deficiency of the u...
AbstractHomozygous mutations of the telomeric survival motor neurone gene (SMN1) cause spinal muscul...
The cell nucleus contains two closely related structures, Cajal bodies (CBs) and gems. CBs are the f...
AbstractHomozygous mutations of the telomeric survival motor neurone gene (SMN1) cause spinal muscul...
International audienceSpinal muscular atrophy (SMA) is caused by reduced levels of the survival of m...
International audienceSpinal muscular atrophy (SMA) is caused by reduced levels of the survival of m...
International audienceSpinal muscular atrophy (SMA) is caused by reduced levels of the survival of m...
AbstractBackground: The survival of motor neurons (SMN) protein is the protein product of the spinal...
International audienceSpinal muscular atrophy is a neuromuscular disease resulting from mutations in...
Spinal muscular atrophy is an autosomal recessive genetic disease that results from the loss and/or ...
AbstractThe survival motor neuron (SMN) protein forms cytoplasmic granules when overexpressed. We re...
Survival motor neuron (SMN) is an essential and ubiquitously expressed protein that participates in ...
Survival motor neuron (SMN) is an essential and ubiquitously expressed protein that participates in ...
Survival motor neuron (SMN) is an essential and ubiquitously expressed protein that participates in ...
Childhood spinal muscular atrophy (SMA) is caused by a reduction in survival motor neuron (SMN) prot...
Proximal spinal muscular atrophy (SMA) is a neurodegenerative disorder caused by deficiency of the u...
AbstractHomozygous mutations of the telomeric survival motor neurone gene (SMN1) cause spinal muscul...
The cell nucleus contains two closely related structures, Cajal bodies (CBs) and gems. CBs are the f...
AbstractHomozygous mutations of the telomeric survival motor neurone gene (SMN1) cause spinal muscul...
International audienceSpinal muscular atrophy (SMA) is caused by reduced levels of the survival of m...
International audienceSpinal muscular atrophy (SMA) is caused by reduced levels of the survival of m...
International audienceSpinal muscular atrophy (SMA) is caused by reduced levels of the survival of m...
AbstractBackground: The survival of motor neurons (SMN) protein is the protein product of the spinal...
International audienceSpinal muscular atrophy is a neuromuscular disease resulting from mutations in...
Spinal muscular atrophy is an autosomal recessive genetic disease that results from the loss and/or ...