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Nerve growth factor transcriptional control of c-fos promoter transfected in cultured spinal sensory neurons
High efficiency gene transfer (greater than 90%) in chicken dorsal root ganglion neurons has been obtained by DNA calcium phosphate co- precipitation, hence providing an important tool to study control of gene expression in primary neurons. Transfection with c-fos promoter sequences linked to the ch...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1992
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2289524/ https://www.ncbi.nlm.nih.gov/pubmed/1618900 |
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collection | PubMed |
description | High efficiency gene transfer (greater than 90%) in chicken dorsal root ganglion neurons has been obtained by DNA calcium phosphate co- precipitation, hence providing an important tool to study control of gene expression in primary neurons. Transfection with c-fos promoter sequences linked to the chloramphenicol acetyltransferase reporter gene showed that the serum responsive element functions as a strong transcriptional enhancer. Transcription from this element is developmentally regulated, and mediates the genetic response to nerve growth factor (NGF) in developing avian sensory neurons. Furthermore, NGF exerts a negative effect on transcription from the cyclic AMP responsive element, thereby supporting the involvement of tyrosine kinase activation by NGF in primary sensory neurons. |
format | Text |
id | pubmed-2289524 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1992 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-22895242008-05-01 Nerve growth factor transcriptional control of c-fos promoter transfected in cultured spinal sensory neurons J Cell Biol Articles High efficiency gene transfer (greater than 90%) in chicken dorsal root ganglion neurons has been obtained by DNA calcium phosphate co- precipitation, hence providing an important tool to study control of gene expression in primary neurons. Transfection with c-fos promoter sequences linked to the chloramphenicol acetyltransferase reporter gene showed that the serum responsive element functions as a strong transcriptional enhancer. Transcription from this element is developmentally regulated, and mediates the genetic response to nerve growth factor (NGF) in developing avian sensory neurons. Furthermore, NGF exerts a negative effect on transcription from the cyclic AMP responsive element, thereby supporting the involvement of tyrosine kinase activation by NGF in primary sensory neurons. The Rockefeller University Press 1992-07-01 /pmc/articles/PMC2289524/ /pubmed/1618900 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Articles Nerve growth factor transcriptional control of c-fos promoter transfected in cultured spinal sensory neurons |
title | Nerve growth factor transcriptional control of c-fos promoter transfected in cultured spinal sensory neurons |
title_full | Nerve growth factor transcriptional control of c-fos promoter transfected in cultured spinal sensory neurons |
title_fullStr | Nerve growth factor transcriptional control of c-fos promoter transfected in cultured spinal sensory neurons |
title_full_unstemmed | Nerve growth factor transcriptional control of c-fos promoter transfected in cultured spinal sensory neurons |
title_short | Nerve growth factor transcriptional control of c-fos promoter transfected in cultured spinal sensory neurons |
title_sort | nerve growth factor transcriptional control of c-fos promoter transfected in cultured spinal sensory neurons |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2289524/ https://www.ncbi.nlm.nih.gov/pubmed/1618900 |