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Neuronal cell-type-specific alternative splicing: A mechanism for specifying connections in the brain?
Alternative splicing (AS) allows a single gene to generate multiple protein isoforms. It has been hypothesized that AS plays a role in brain wiring by increasing the number of cell recognition molecules necessary for forming connections between neurons. Many studies have characterized isoform expres...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4973604/ https://www.ncbi.nlm.nih.gov/pubmed/27606331 http://dx.doi.org/10.1080/23262133.2015.1122699 |
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author | Li, Joshua Shing Shun Shin, Grace Ji-eun Millard, S Sean |
author_facet | Li, Joshua Shing Shun Shin, Grace Ji-eun Millard, S Sean |
author_sort | Li, Joshua Shing Shun |
collection | PubMed |
description | Alternative splicing (AS) allows a single gene to generate multiple protein isoforms. It has been hypothesized that AS plays a role in brain wiring by increasing the number of cell recognition molecules necessary for forming connections between neurons. Many studies have characterized isoform expression patterns of various genes in the brain, but very few have addressed whether specific isoforms play a functional role in neuronal wiring. In our recent work, we reported the cell-type-specific AS of the cell recognition molecule Dscam2. Exclusive expression of Dscam2 isoforms allows tightly associated neurons to signal repulsion selectively within the same cell-types, without interfering with one another. We show that preventing cell-specific isoform expression in 2 closely associated neurons disrupts their axon terminal morphology. We propose that the requirement for isoform specificity extends to synapses and discuss experiments that can test this directly. Factors that regulate Dscam2 cell-type-specific AS likely regulate the splicing of many genes involved in neurodevelopment. These regulators of alternative splicing may act broadly to control many genes involved in the development of specific neuron types. Identifying these factors is a key step in understanding how AS contributes to the brain connectome. |
format | Online Article Text |
id | pubmed-4973604 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-49736042016-12-15 Neuronal cell-type-specific alternative splicing: A mechanism for specifying connections in the brain? Li, Joshua Shing Shun Shin, Grace Ji-eun Millard, S Sean Neurogenesis (Austin) Commentary Alternative splicing (AS) allows a single gene to generate multiple protein isoforms. It has been hypothesized that AS plays a role in brain wiring by increasing the number of cell recognition molecules necessary for forming connections between neurons. Many studies have characterized isoform expression patterns of various genes in the brain, but very few have addressed whether specific isoforms play a functional role in neuronal wiring. In our recent work, we reported the cell-type-specific AS of the cell recognition molecule Dscam2. Exclusive expression of Dscam2 isoforms allows tightly associated neurons to signal repulsion selectively within the same cell-types, without interfering with one another. We show that preventing cell-specific isoform expression in 2 closely associated neurons disrupts their axon terminal morphology. We propose that the requirement for isoform specificity extends to synapses and discuss experiments that can test this directly. Factors that regulate Dscam2 cell-type-specific AS likely regulate the splicing of many genes involved in neurodevelopment. These regulators of alternative splicing may act broadly to control many genes involved in the development of specific neuron types. Identifying these factors is a key step in understanding how AS contributes to the brain connectome. Taylor & Francis 2015-12-15 /pmc/articles/PMC4973604/ /pubmed/27606331 http://dx.doi.org/10.1080/23262133.2015.1122699 Text en © 2015 The Author(s). Published with license by Taylor & Francis http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted. |
spellingShingle | Commentary Li, Joshua Shing Shun Shin, Grace Ji-eun Millard, S Sean Neuronal cell-type-specific alternative splicing: A mechanism for specifying connections in the brain? |
title | Neuronal cell-type-specific alternative splicing: A mechanism for specifying connections in the brain? |
title_full | Neuronal cell-type-specific alternative splicing: A mechanism for specifying connections in the brain? |
title_fullStr | Neuronal cell-type-specific alternative splicing: A mechanism for specifying connections in the brain? |
title_full_unstemmed | Neuronal cell-type-specific alternative splicing: A mechanism for specifying connections in the brain? |
title_short | Neuronal cell-type-specific alternative splicing: A mechanism for specifying connections in the brain? |
title_sort | neuronal cell-type-specific alternative splicing: a mechanism for specifying connections in the brain? |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4973604/ https://www.ncbi.nlm.nih.gov/pubmed/27606331 http://dx.doi.org/10.1080/23262133.2015.1122699 |
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