Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Joshua Shing Shun, Shin, Grace Ji-eun, Millard, S Sean
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2015
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
_version_ 1782446424437293056
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
work_keys_str_mv AT lijoshuashingshun neuronalcelltypespecificalternativesplicingamechanismforspecifyingconnectionsinthebrain
AT shingracejieun neuronalcelltypespecificalternativesplicingamechanismforspecifyingconnectionsinthebrain
AT millardssean neuronalcelltypespecificalternativesplicingamechanismforspecifyingconnectionsinthebrain