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TPM3 and TPM4 gene products segregate to the postsynaptic region of central nervous system synapses
Synaptic function in the central nervous system (CNS) is highly dependent on a dynamic actin cytoskeleton in both the pre- and the postsynaptic compartment. Remodelling of the actin cytoskeleton is controlled by tropomyosins, a family of actin-associated proteins which define distinct actin filament...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Landes Bioscience
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3337131/ https://www.ncbi.nlm.nih.gov/pubmed/22545181 http://dx.doi.org/10.4161/bioa.1.6.19336 |
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author | Guven, Kim Gunning, Peter Fath, Thomas |
author_facet | Guven, Kim Gunning, Peter Fath, Thomas |
author_sort | Guven, Kim |
collection | PubMed |
description | Synaptic function in the central nervous system (CNS) is highly dependent on a dynamic actin cytoskeleton in both the pre- and the postsynaptic compartment. Remodelling of the actin cytoskeleton is controlled by tropomyosins, a family of actin-associated proteins which define distinct actin filament populations. Here we show that TPM3 and TPM4 gene products localize to the postsynaptic region in mouse hippocampal neurons. Furthermore our data confirm previous findings of isoform segregation to the pre- and postsynaptic compartments at CNS synapses. These data provide fundamental insights in the formation of functionally distinct actin filament populations at the pre- and post-synapse. |
format | Online Article Text |
id | pubmed-3337131 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Landes Bioscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-33371312012-05-07 TPM3 and TPM4 gene products segregate to the postsynaptic region of central nervous system synapses Guven, Kim Gunning, Peter Fath, Thomas Bioarchitecture Short Communication Synaptic function in the central nervous system (CNS) is highly dependent on a dynamic actin cytoskeleton in both the pre- and the postsynaptic compartment. Remodelling of the actin cytoskeleton is controlled by tropomyosins, a family of actin-associated proteins which define distinct actin filament populations. Here we show that TPM3 and TPM4 gene products localize to the postsynaptic region in mouse hippocampal neurons. Furthermore our data confirm previous findings of isoform segregation to the pre- and postsynaptic compartments at CNS synapses. These data provide fundamental insights in the formation of functionally distinct actin filament populations at the pre- and post-synapse. Landes Bioscience 2011-11-01 /pmc/articles/PMC3337131/ /pubmed/22545181 http://dx.doi.org/10.4161/bioa.1.6.19336 Text en Copyright © 2011 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Short Communication Guven, Kim Gunning, Peter Fath, Thomas TPM3 and TPM4 gene products segregate to the postsynaptic region of central nervous system synapses |
title | TPM3 and TPM4 gene products segregate to the postsynaptic region of central nervous system synapses |
title_full | TPM3 and TPM4 gene products segregate to the postsynaptic region of central nervous system synapses |
title_fullStr | TPM3 and TPM4 gene products segregate to the postsynaptic region of central nervous system synapses |
title_full_unstemmed | TPM3 and TPM4 gene products segregate to the postsynaptic region of central nervous system synapses |
title_short | TPM3 and TPM4 gene products segregate to the postsynaptic region of central nervous system synapses |
title_sort | tpm3 and tpm4 gene products segregate to the postsynaptic region of central nervous system synapses |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3337131/ https://www.ncbi.nlm.nih.gov/pubmed/22545181 http://dx.doi.org/10.4161/bioa.1.6.19336 |
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