Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1999-4-1
pubmed:abstractText
Spinal muscular atrophy (SMA) is among the most common recessive autosomal diseases and is characterized by the loss of spinal motor neurons. A gene termed 'Survival of Motor Neurons' (SMN) has been identified as the SMA-determining gene. Recent work indicates the involvement of the SMN protein and its associated protein SIP1 in spliceosomal snRNP biogenesis. However, the function of SMN remains unknown. Here, we have studied the subcellular localization of SMN in the rat spinal cord and more generally in the central nervous system (CNS), by light fluorescence and electron microscopy. SMN immunoreactivity (IR) was found in the different regions of the spinal cord but also in various regions of the CNS such as the brainstem, cerebellum, thalamus, cortex and hippocampus. In most neurons, we observed a speckled labelling of the cytoplasm and a discontinuous staining of the nuclear envelope. For some neurons (e.g. brainstem nuclei, dentate gyrus, cortex: layer V) and, in particular in motoneurons, SMN-IR was also present as prominent nuclear dot-like-structures. In these nuclear dots, SMN colocalized with SIP1 and with fibrillarin, a marker of coiled bodies. Ultrastructural studies in the anterior horn of the spinal cord confirmed the presence of SMN in the coiled bodies and also revealed the protein at the external side of nuclear pores complexes, in association with polyribosomes, and in dendrites, associated with microtubules. These localizations suggest that, in addition to its involvement in the spliceosome biogenesis, the SMN protein could also play a part in nucleocytoplasmic and dendritic transport.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0953-816X
pubmed:author
pubmed:issnType
Print
pubmed:volume
11
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
293-304
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:9987032-Animals, pubmed-meshheading:9987032-Biological Transport, pubmed-meshheading:9987032-Cell Compartmentation, pubmed-meshheading:9987032-Cyclic AMP Response Element-Binding Protein, pubmed-meshheading:9987032-Cytoplasm, pubmed-meshheading:9987032-Dendrites, pubmed-meshheading:9987032-Fetus, pubmed-meshheading:9987032-Fluorescent Antibody Technique, pubmed-meshheading:9987032-Microscopy, Immunoelectron, pubmed-meshheading:9987032-Motor Neurons, pubmed-meshheading:9987032-Nerve Tissue Proteins, pubmed-meshheading:9987032-Nuclear Envelope, pubmed-meshheading:9987032-RNA-Binding Proteins, pubmed-meshheading:9987032-Rabbits, pubmed-meshheading:9987032-Rats, pubmed-meshheading:9987032-Rats, Sprague-Dawley, pubmed-meshheading:9987032-SMN Complex Proteins, pubmed-meshheading:9987032-Spinal Cord, pubmed-meshheading:9987032-Survival of Motor Neuron 1 Protein
pubmed:year
1999
pubmed:articleTitle
Subcellular distribution of survival motor neuron (SMN) protein: possible involvement in nucleocytoplasmic and dendritic transport.
pubmed:affiliation
Laboratoire de Biologie Cellulaire de la Synapse Normale et Pathologique (INSERM U497), Paris, France.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't