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Teneurin-1 is expressed in interconnected regions of the developing brain and is processed in vivo

BACKGROUND: Teneurins are a unique family of transmembrane proteins conserved from C. elegans and D. melanogaster to mammals. In vertebrates there are four paralogs (teneurin-1 to -4), all of which are expressed prominently in the developing central nervous system. RESULTS: Analysis of teneurin-1 ex...

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Autores principales: Kenzelmann, Daniela, Chiquet-Ehrismann, Ruth, Leachman, Nathaniel T, Tucker, Richard P
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2289808/
https://www.ncbi.nlm.nih.gov/pubmed/18366734
http://dx.doi.org/10.1186/1471-213X-8-30
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author Kenzelmann, Daniela
Chiquet-Ehrismann, Ruth
Leachman, Nathaniel T
Tucker, Richard P
author_facet Kenzelmann, Daniela
Chiquet-Ehrismann, Ruth
Leachman, Nathaniel T
Tucker, Richard P
author_sort Kenzelmann, Daniela
collection PubMed
description BACKGROUND: Teneurins are a unique family of transmembrane proteins conserved from C. elegans and D. melanogaster to mammals. In vertebrates there are four paralogs (teneurin-1 to -4), all of which are expressed prominently in the developing central nervous system. RESULTS: Analysis of teneurin-1 expression in the developing chick brain by in situ hybridization and immunohistochemistry defined a unique, distinct expression pattern in interconnected regions of the brain. Moreover we found complementary patterns of teneurin-1 and-2 expression in many parts of the brain, including the retina, optic tectum, olfactory bulb, and cerebellum as well as in brain nuclei involved in processing of sensory information. Based on these expression patterns, we suspect a role for teneurins in neuronal connectivity. In contrast to the cell-surface staining of the antibody against the extracellular domain, an antibody recognizing the intracellular domain revealed nuclear staining in subpopulations of neurons and in undifferentiated mesenchyme. Western blot analysis of brain lysates showed the presence of N-terminal fragments of teneurin-1 containing the intracellular domain indicating that proteolytic processing occurs. Finally, the teneurin-1 intracellular domain was found to contain a nuclear localization signal, which is required for nuclear localization in transfected cells. CONCLUSION: Teneurin-1 and -2 are expressed by distinct interconnected populations of neurons in the developing central nervous system. Our data support the hypothesis that teneurins can be proteolytically processed leading to the release of the intracellular domain and its translocation to the nucleus.
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spelling pubmed-22898082008-04-08 Teneurin-1 is expressed in interconnected regions of the developing brain and is processed in vivo Kenzelmann, Daniela Chiquet-Ehrismann, Ruth Leachman, Nathaniel T Tucker, Richard P BMC Dev Biol Research Article BACKGROUND: Teneurins are a unique family of transmembrane proteins conserved from C. elegans and D. melanogaster to mammals. In vertebrates there are four paralogs (teneurin-1 to -4), all of which are expressed prominently in the developing central nervous system. RESULTS: Analysis of teneurin-1 expression in the developing chick brain by in situ hybridization and immunohistochemistry defined a unique, distinct expression pattern in interconnected regions of the brain. Moreover we found complementary patterns of teneurin-1 and-2 expression in many parts of the brain, including the retina, optic tectum, olfactory bulb, and cerebellum as well as in brain nuclei involved in processing of sensory information. Based on these expression patterns, we suspect a role for teneurins in neuronal connectivity. In contrast to the cell-surface staining of the antibody against the extracellular domain, an antibody recognizing the intracellular domain revealed nuclear staining in subpopulations of neurons and in undifferentiated mesenchyme. Western blot analysis of brain lysates showed the presence of N-terminal fragments of teneurin-1 containing the intracellular domain indicating that proteolytic processing occurs. Finally, the teneurin-1 intracellular domain was found to contain a nuclear localization signal, which is required for nuclear localization in transfected cells. CONCLUSION: Teneurin-1 and -2 are expressed by distinct interconnected populations of neurons in the developing central nervous system. Our data support the hypothesis that teneurins can be proteolytically processed leading to the release of the intracellular domain and its translocation to the nucleus. BioMed Central 2008-03-25 /pmc/articles/PMC2289808/ /pubmed/18366734 http://dx.doi.org/10.1186/1471-213X-8-30 Text en Copyright © 2008 Kenzelmann et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Kenzelmann, Daniela
Chiquet-Ehrismann, Ruth
Leachman, Nathaniel T
Tucker, Richard P
Teneurin-1 is expressed in interconnected regions of the developing brain and is processed in vivo
title Teneurin-1 is expressed in interconnected regions of the developing brain and is processed in vivo
title_full Teneurin-1 is expressed in interconnected regions of the developing brain and is processed in vivo
title_fullStr Teneurin-1 is expressed in interconnected regions of the developing brain and is processed in vivo
title_full_unstemmed Teneurin-1 is expressed in interconnected regions of the developing brain and is processed in vivo
title_short Teneurin-1 is expressed in interconnected regions of the developing brain and is processed in vivo
title_sort teneurin-1 is expressed in interconnected regions of the developing brain and is processed in vivo
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2289808/
https://www.ncbi.nlm.nih.gov/pubmed/18366734
http://dx.doi.org/10.1186/1471-213X-8-30
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