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How genetically engineered systems are helping to define, and in some cases redefine, the neurobiological basis of sleep and wake

The advent of genetically engineered systems, including transgenic animals and recombinant viral vectors, has facilitated a more detailed understanding of the molecular and cellular substrates regulating brain function. In this review we highlight some of the most recent molecular biology and geneti...

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Autores principales: Fuller, Patrick M, Yamanaka, Akihiro, Lazarus, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4843941/
https://www.ncbi.nlm.nih.gov/pubmed/27227054
http://dx.doi.org/10.1080/23328940.2015.1075095
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author Fuller, Patrick M
Yamanaka, Akihiro
Lazarus, Michael
author_facet Fuller, Patrick M
Yamanaka, Akihiro
Lazarus, Michael
author_sort Fuller, Patrick M
collection PubMed
description The advent of genetically engineered systems, including transgenic animals and recombinant viral vectors, has facilitated a more detailed understanding of the molecular and cellular substrates regulating brain function. In this review we highlight some of the most recent molecular biology and genetic technologies in the experimental “systems neurosciences,” many of which are rapidly becoming a methodological standard, and focus in particular on those tools and techniques that permit the reversible and cell-type specific manipulation of neurons in behaving animals. These newer techniques encompass a wide range of approaches including conditional deletion of genes based on Cre/loxP technology, gene silencing using RNA interference, cell-type specific mapping or ablation and reversible manipulation (silencing and activation) of neurons in vivo. Combining these approaches with viral vector delivery systems, in particular adeno-associated viruses (AAV), has extended, in some instances greatly, the utility of these tools. For example, the spatially- and/or temporally-restricted transduction of specific neuronal cell populations is now routinely achieved using the combination of Cre-driver mice and stereotaxic-based delivery of AAV expressing Cre-dependent cassettes. We predict that the experimental application of these tools, including creative combinatorial approaches and the development of even newer reagents, will prove necessary for a complete understanding of the neuronal circuits subserving most neurobiological functions, including the regulation of sleep and wake.
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spelling pubmed-48439412016-05-25 How genetically engineered systems are helping to define, and in some cases redefine, the neurobiological basis of sleep and wake Fuller, Patrick M Yamanaka, Akihiro Lazarus, Michael Temperature (Austin) Review The advent of genetically engineered systems, including transgenic animals and recombinant viral vectors, has facilitated a more detailed understanding of the molecular and cellular substrates regulating brain function. In this review we highlight some of the most recent molecular biology and genetic technologies in the experimental “systems neurosciences,” many of which are rapidly becoming a methodological standard, and focus in particular on those tools and techniques that permit the reversible and cell-type specific manipulation of neurons in behaving animals. These newer techniques encompass a wide range of approaches including conditional deletion of genes based on Cre/loxP technology, gene silencing using RNA interference, cell-type specific mapping or ablation and reversible manipulation (silencing and activation) of neurons in vivo. Combining these approaches with viral vector delivery systems, in particular adeno-associated viruses (AAV), has extended, in some instances greatly, the utility of these tools. For example, the spatially- and/or temporally-restricted transduction of specific neuronal cell populations is now routinely achieved using the combination of Cre-driver mice and stereotaxic-based delivery of AAV expressing Cre-dependent cassettes. We predict that the experimental application of these tools, including creative combinatorial approaches and the development of even newer reagents, will prove necessary for a complete understanding of the neuronal circuits subserving most neurobiological functions, including the regulation of sleep and wake. Taylor & Francis 2015-10-12 /pmc/articles/PMC4843941/ /pubmed/27227054 http://dx.doi.org/10.1080/23328940.2015.1075095 Text en © 2015 The Author(s). Published with license by Taylor & Francis Group, LLC 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 Review
Fuller, Patrick M
Yamanaka, Akihiro
Lazarus, Michael
How genetically engineered systems are helping to define, and in some cases redefine, the neurobiological basis of sleep and wake
title How genetically engineered systems are helping to define, and in some cases redefine, the neurobiological basis of sleep and wake
title_full How genetically engineered systems are helping to define, and in some cases redefine, the neurobiological basis of sleep and wake
title_fullStr How genetically engineered systems are helping to define, and in some cases redefine, the neurobiological basis of sleep and wake
title_full_unstemmed How genetically engineered systems are helping to define, and in some cases redefine, the neurobiological basis of sleep and wake
title_short How genetically engineered systems are helping to define, and in some cases redefine, the neurobiological basis of sleep and wake
title_sort how genetically engineered systems are helping to define, and in some cases redefine, the neurobiological basis of sleep and wake
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4843941/
https://www.ncbi.nlm.nih.gov/pubmed/27227054
http://dx.doi.org/10.1080/23328940.2015.1075095
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