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Dscam1 in Pancrustacean Immunity: Current Status and a Look to the Future
The Down syndrome cell adhesion molecule 1 (Dscam1) gene is an extraordinary example of diversity: by combining alternatively spliced exons, thousands of isoforms can be produced from just one gene. So far, such diversity in this gene has only been found in insects and crustaceans, and its essential...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5465998/ https://www.ncbi.nlm.nih.gov/pubmed/28649249 http://dx.doi.org/10.3389/fimmu.2017.00662 |
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author | Armitage, Sophie A. O. Kurtz, Joachim Brites, Daniela Dong, Yuemei Du Pasquier, Louis Wang, Han-Ching |
author_facet | Armitage, Sophie A. O. Kurtz, Joachim Brites, Daniela Dong, Yuemei Du Pasquier, Louis Wang, Han-Ching |
author_sort | Armitage, Sophie A. O. |
collection | PubMed |
description | The Down syndrome cell adhesion molecule 1 (Dscam1) gene is an extraordinary example of diversity: by combining alternatively spliced exons, thousands of isoforms can be produced from just one gene. So far, such diversity in this gene has only been found in insects and crustaceans, and its essential part in neural wiring has been well-characterized for Drosophila melanogaster. Ten years ago evidence from D. melanogaster showed that the Dscam1 gene is involved in insect immune defense and work on Anopheles gambiae indicated that it is a hypervariable immune receptor. These exciting findings showed that via processes of somatic diversification insects have the possibility to produce unexpected immune molecule diversity, and it was hypothesized that Dscam1 could provide the mechanistic underpinnings of specific immune responses. Since these first publications the quest to understand the function of this gene has uncovered fascinating insights from insects and crustaceans. However, we are still far from a complete understanding of how Dscam1 functions in relation to parasites and pathogens and its full relevance for the immune system. In this Hypothesis and Theory article, we first briefly introduce Dscam1 and what we know so far about how it might function in immunity. By focusing on seven questions, we then share our sometimes contrasting thoughts on what the evidence tells us so far, what essential experiments remain to be done, and the future prospects, with the aim to provide a multiangled view on what this fascinating gene has to do with immune defense. |
format | Online Article Text |
id | pubmed-5465998 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54659982017-06-23 Dscam1 in Pancrustacean Immunity: Current Status and a Look to the Future Armitage, Sophie A. O. Kurtz, Joachim Brites, Daniela Dong, Yuemei Du Pasquier, Louis Wang, Han-Ching Front Immunol Immunology The Down syndrome cell adhesion molecule 1 (Dscam1) gene is an extraordinary example of diversity: by combining alternatively spliced exons, thousands of isoforms can be produced from just one gene. So far, such diversity in this gene has only been found in insects and crustaceans, and its essential part in neural wiring has been well-characterized for Drosophila melanogaster. Ten years ago evidence from D. melanogaster showed that the Dscam1 gene is involved in insect immune defense and work on Anopheles gambiae indicated that it is a hypervariable immune receptor. These exciting findings showed that via processes of somatic diversification insects have the possibility to produce unexpected immune molecule diversity, and it was hypothesized that Dscam1 could provide the mechanistic underpinnings of specific immune responses. Since these first publications the quest to understand the function of this gene has uncovered fascinating insights from insects and crustaceans. However, we are still far from a complete understanding of how Dscam1 functions in relation to parasites and pathogens and its full relevance for the immune system. In this Hypothesis and Theory article, we first briefly introduce Dscam1 and what we know so far about how it might function in immunity. By focusing on seven questions, we then share our sometimes contrasting thoughts on what the evidence tells us so far, what essential experiments remain to be done, and the future prospects, with the aim to provide a multiangled view on what this fascinating gene has to do with immune defense. Frontiers Media S.A. 2017-06-09 /pmc/articles/PMC5465998/ /pubmed/28649249 http://dx.doi.org/10.3389/fimmu.2017.00662 Text en Copyright © 2017 Armitage, Kurtz, Brites, Dong, Du Pasquier and Wang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Armitage, Sophie A. O. Kurtz, Joachim Brites, Daniela Dong, Yuemei Du Pasquier, Louis Wang, Han-Ching Dscam1 in Pancrustacean Immunity: Current Status and a Look to the Future |
title | Dscam1 in Pancrustacean Immunity: Current Status and a Look to the Future |
title_full | Dscam1 in Pancrustacean Immunity: Current Status and a Look to the Future |
title_fullStr | Dscam1 in Pancrustacean Immunity: Current Status and a Look to the Future |
title_full_unstemmed | Dscam1 in Pancrustacean Immunity: Current Status and a Look to the Future |
title_short | Dscam1 in Pancrustacean Immunity: Current Status and a Look to the Future |
title_sort | dscam1 in pancrustacean immunity: current status and a look to the future |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5465998/ https://www.ncbi.nlm.nih.gov/pubmed/28649249 http://dx.doi.org/10.3389/fimmu.2017.00662 |
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