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The Journal of Neuroscience, October 1, 2002, 22(19):8347-8351
BRIEF COMMUNICATION
Repressor Element-1 Silencing Transcription/Neuron-Restrictive
Silencer Factor Is Required for Neural Sodium Channel Expression
during Development of Xenopus
Ricardo
Armisén*,
Rómulo
Fuentes*,
Patricio
Olguín,
María E.
Cabrejos, and
Manuel
Kukuljan
Programa de Fisiología y Biofísica, Instituto de
Ciencias Biomédicas, Facultad de Medicina, Universidad de Chile,
Independencia 1027, Santiago, Chile
The ability of neurons to fire rapid action potential relies on the
expression of voltage-gated sodium channels; the onset of the
transcription of genes that encode these channels occurs during early
neuronal development. The factors that direct and regulate the specific
expression of ion channels are not well understood. Repressor element-1
silencing transcription/neuron-restrictive silencer factor
(REST/NRSF) is a transcriptional regulator characterized as a repressor
of the expression of NaV1.2, the gene encoding the voltage-gated sodium channel most abundantly expressed in the CNS,
as well as of the expression of numerous other neuronal genes. In
mammals, REST/NRSF is expressed mostly in non-neural cell types and
immature neurons, and it is downregulated on neural maturation. To
understand the mechanisms that govern sodium channel gene transcription
and to explore the role of REST/NRSF in vivo, we
inhibited REST/NRSF action in developing Xenopus
laevis embryos by means of a dominant negative protein
or antisense oligonucleotides. Contrary to what was expected, these
maneuvers result in the decrease of the expression of the
NaV1.2 gene, as well as of other neuronal genes in the
primary spinal neurons and cranial ganglia, without overt perturbation
of neurogenesis. These results, together with the demonstration of
robust REST/NRSF expression in primary spinal neurons, suggest that
REST/NRSF is required for the acquisition of the differentiated
functional neuronal phenotype during early development. Furthermore,
they suggest that REST/NRSF may be used to activate or repress
transcription of neuronal genes in distinct cellular and developmental contexts.
Key words:
primary spinal neurons; neuronal differentiation; repressor element silencer of transcription; dominant negative; antisense oligonucleotides; sodium channels
*
R.A. and R.F. contributed equally to this work.
Copyright © 2002 Society for Neuroscience 0270-6474/02/22198347-05$05.00/0
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