Human Molecular Genetics, Vol 8, 2133-2143, Copyright © 1999 by Oxford University Press
I Miguel-Aliaga, E Culetto, DS Walker, HA Baylis, DB Sattelle and KE Davies
Spinal muscular atrophy (SMA) is a common disorder characterized by loss of
lower motor neurones of the spinal cord. The disease is caused by mutations
in the survival motor neurone ( SMN ) gene. SMN is ubiquitously expressed
and evolutionarily conserved, and its role in RNA processing has been well
established. However, these properties do not explain the observed
specificity of motor neurone death. To gain further insight into the
function of SMN, we have isolated and characterized the Caenorhabditis
elegans orthologue of the SMN gene ( CeSMN ). Here we show that CeSMN is
transmitted maternally as a predominantly nuclear factor, which remains
present in all the blastomeres throughout embryonic development and onwards
into adulthood. In adult nematodes, a CeSMN-green fluorescent protein
fusion protein is expressed in a number of cell types including the
germline. Both disruption of the endogenous CeSMN function and
overexpression of the gene result in a severe decrease in the number of
progeny and in locomotive defects. In addition, its transient knockdown
leads to sterility caused by a defect in germ cell maturation. The
expression pattern and functional properties so far observed for CeSMN,
together with its unusual behaviour in the germline, indicate that SMN may
be involved in specific gene expression events at these very early
developmental stages. We have also identified a deletion in the CeSMN
promoter region in egl-32. This mutant may become a useful genetic tool
with which to explore regulation of CeSMN and hence provide possible clues
for novel therapeutic strategies for SMA.
ARTICLES
The Caenorhabditis elegans orthologue of the human gene responsible for spinal muscular atrophy is a maternal product critical for germline maturation and embryonic viability
Department of Human Anatomy and Genetics, University of Oxford, South Parks Road, Oxford OX1 3QX, UK,
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