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Differential Spatial Expression and Subcellular Localization of CtBP Family Members in Rodent Brain
C-terminal binding proteins (CtBPs) are well-characterized nuclear transcriptional co-regulators. In addition, cytoplasmic functions were discovered for these ubiquitously expressed proteins. These include the involvement of the isoform CtBP1-S/BARS50 in cellular membrane-trafficking processes and a...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3382178/ https://www.ncbi.nlm.nih.gov/pubmed/22745816 http://dx.doi.org/10.1371/journal.pone.0039710 |
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author | Hübler, Diana Rankovic, Marija Richter, Karin Lazarevic, Vesna Altrock, Wilko D. Fischer, Klaus-Dieter Gundelfinger, Eckart D. Fejtova, Anna |
author_facet | Hübler, Diana Rankovic, Marija Richter, Karin Lazarevic, Vesna Altrock, Wilko D. Fischer, Klaus-Dieter Gundelfinger, Eckart D. Fejtova, Anna |
author_sort | Hübler, Diana |
collection | PubMed |
description | C-terminal binding proteins (CtBPs) are well-characterized nuclear transcriptional co-regulators. In addition, cytoplasmic functions were discovered for these ubiquitously expressed proteins. These include the involvement of the isoform CtBP1-S/BARS50 in cellular membrane-trafficking processes and a role of the isoform RIBEYE as molecular scaffolds in ribbons, the presynaptic specializations of sensory synapses. CtBPs were suggested to regulate neuronal differentiation and they were implied in the control of gene expression during epileptogenesis. However, the expression patterns of CtBP family members in specific brain areas and their subcellular localizations in neurons in situ are largely unknown. Here, we performed comprehensive assessment of the expression of CtBP1 and CtBP2 in mouse brain at the microscopic and the ultra-structural levels using specific antibodies. We quantified and compared expression levels of both CtBPs in biochemically isolated brain fractions containing cellular nuclei or synaptic compartment. Our study demonstrates differential regional and subcellular expression patterns for the two CtBP family members in brain and reveals a previously unknown synaptic localization for CtBP2 in particular brain regions. Finally, we propose a mechanism of differential synapto-nuclear targeting of its splice variants CtBP2-S and CtBP2-L in neurons. |
format | Online Article Text |
id | pubmed-3382178 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33821782012-06-28 Differential Spatial Expression and Subcellular Localization of CtBP Family Members in Rodent Brain Hübler, Diana Rankovic, Marija Richter, Karin Lazarevic, Vesna Altrock, Wilko D. Fischer, Klaus-Dieter Gundelfinger, Eckart D. Fejtova, Anna PLoS One Research Article C-terminal binding proteins (CtBPs) are well-characterized nuclear transcriptional co-regulators. In addition, cytoplasmic functions were discovered for these ubiquitously expressed proteins. These include the involvement of the isoform CtBP1-S/BARS50 in cellular membrane-trafficking processes and a role of the isoform RIBEYE as molecular scaffolds in ribbons, the presynaptic specializations of sensory synapses. CtBPs were suggested to regulate neuronal differentiation and they were implied in the control of gene expression during epileptogenesis. However, the expression patterns of CtBP family members in specific brain areas and their subcellular localizations in neurons in situ are largely unknown. Here, we performed comprehensive assessment of the expression of CtBP1 and CtBP2 in mouse brain at the microscopic and the ultra-structural levels using specific antibodies. We quantified and compared expression levels of both CtBPs in biochemically isolated brain fractions containing cellular nuclei or synaptic compartment. Our study demonstrates differential regional and subcellular expression patterns for the two CtBP family members in brain and reveals a previously unknown synaptic localization for CtBP2 in particular brain regions. Finally, we propose a mechanism of differential synapto-nuclear targeting of its splice variants CtBP2-S and CtBP2-L in neurons. Public Library of Science 2012-06-22 /pmc/articles/PMC3382178/ /pubmed/22745816 http://dx.doi.org/10.1371/journal.pone.0039710 Text en This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Hübler, Diana Rankovic, Marija Richter, Karin Lazarevic, Vesna Altrock, Wilko D. Fischer, Klaus-Dieter Gundelfinger, Eckart D. Fejtova, Anna Differential Spatial Expression and Subcellular Localization of CtBP Family Members in Rodent Brain |
title | Differential Spatial Expression and Subcellular Localization of CtBP Family Members in Rodent Brain |
title_full | Differential Spatial Expression and Subcellular Localization of CtBP Family Members in Rodent Brain |
title_fullStr | Differential Spatial Expression and Subcellular Localization of CtBP Family Members in Rodent Brain |
title_full_unstemmed | Differential Spatial Expression and Subcellular Localization of CtBP Family Members in Rodent Brain |
title_short | Differential Spatial Expression and Subcellular Localization of CtBP Family Members in Rodent Brain |
title_sort | differential spatial expression and subcellular localization of ctbp family members in rodent brain |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3382178/ https://www.ncbi.nlm.nih.gov/pubmed/22745816 http://dx.doi.org/10.1371/journal.pone.0039710 |
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