Repressor element-1 silencing transcription/neuron-restrictive silencer factor is required for neural sodium channel expression during development of Xenopus
Author
dc.contributor.author
Armisen Yáñez, Ricardo
Author
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Fuentes, Rómulo
Author
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Olguín, Patricio
Author
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Cabrejos, María E.
Author
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Kukuljan Padilla, Manuel
Admission date
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2019-01-29T17:51:49Z
Available date
dc.date.available
2019-01-29T17:51:49Z
Publication date
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2002
Cita de ítem
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Journal of Neuroscience, Volumen 22, Issue 19, 2018, Pages 8347-8351
Identifier
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02706474
Identifier
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https://repositorio.uchile.cl/handle/2250/163579
Abstract
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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 domina
Repressor element-1 silencing transcription/neuron-restrictive silencer factor is required for neural sodium channel expression during development of Xenopus