Avian adeno-associated virus vector efficiently transduces neurons in the embryonic and post-embryonic chicken brain.

The domestic chicken is an attractive model system to explore the development and function of brain circuits. Electroporation-mediated and retrovirus (including lentivirus) vector-mediated gene transfer techniques have been widely used to introduce genetic material into chicken cells. However, it is...

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Main Authors: Ryosuke Matsui, Yasuto Tanabe, Dai Watanabe
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23144948/?tool=EBI
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spelling doaj-fa234d0e442f4e35a4eebab530affdfc2021-03-03T20:26:43ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-01711e4873010.1371/journal.pone.0048730Avian adeno-associated virus vector efficiently transduces neurons in the embryonic and post-embryonic chicken brain.Ryosuke MatsuiYasuto TanabeDai WatanabeThe domestic chicken is an attractive model system to explore the development and function of brain circuits. Electroporation-mediated and retrovirus (including lentivirus) vector-mediated gene transfer techniques have been widely used to introduce genetic material into chicken cells. However, it is still challenging to efficiently transduce chicken postmitotic neurons without harming the cells. To overcome this problem, we searched for a virus vector suitable for gene transfer into chicken neurons, and report here a novel recombinant virus vector derived from avian adeno-associated virus (A3V). A3V vector efficiently transduces neuronal cells, but not non-neuronal cells in the brain. A single A3V injection into a postembryonic chick brain allows gene expression selectively in neuronal cells within 24 hrs. Such rapid and neuron-specific gene transduction raises the possibility that A3V vector can be utilized for studies of memory formation in filial imprinting, which occurs during the early postnatal days. A3V injection into the neural tube near the ear vesicle at early embryonic stage resulted in persistent and robust gene expression until E20.5 in the auditory brainstem. We further devised an A3V-mediated tetracycline (Tet) dependent gene expression system as a tool for studying the auditory circuit, consisting of the nucleus magnocellularis (NM) and nucleus laminaris (NL), that primarily computes interaural time differences (ITDs). Using this Tet system, we can transduce NM neurons without affecting NL neurons. Thus, the A3V technology complements current gene transfer techniques in chicken studies and will contribute to better understanding of the functional organization of neural circuits.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23144948/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Ryosuke Matsui
Yasuto Tanabe
Dai Watanabe
spellingShingle Ryosuke Matsui
Yasuto Tanabe
Dai Watanabe
Avian adeno-associated virus vector efficiently transduces neurons in the embryonic and post-embryonic chicken brain.
PLoS ONE
author_facet Ryosuke Matsui
Yasuto Tanabe
Dai Watanabe
author_sort Ryosuke Matsui
title Avian adeno-associated virus vector efficiently transduces neurons in the embryonic and post-embryonic chicken brain.
title_short Avian adeno-associated virus vector efficiently transduces neurons in the embryonic and post-embryonic chicken brain.
title_full Avian adeno-associated virus vector efficiently transduces neurons in the embryonic and post-embryonic chicken brain.
title_fullStr Avian adeno-associated virus vector efficiently transduces neurons in the embryonic and post-embryonic chicken brain.
title_full_unstemmed Avian adeno-associated virus vector efficiently transduces neurons in the embryonic and post-embryonic chicken brain.
title_sort avian adeno-associated virus vector efficiently transduces neurons in the embryonic and post-embryonic chicken brain.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description The domestic chicken is an attractive model system to explore the development and function of brain circuits. Electroporation-mediated and retrovirus (including lentivirus) vector-mediated gene transfer techniques have been widely used to introduce genetic material into chicken cells. However, it is still challenging to efficiently transduce chicken postmitotic neurons without harming the cells. To overcome this problem, we searched for a virus vector suitable for gene transfer into chicken neurons, and report here a novel recombinant virus vector derived from avian adeno-associated virus (A3V). A3V vector efficiently transduces neuronal cells, but not non-neuronal cells in the brain. A single A3V injection into a postembryonic chick brain allows gene expression selectively in neuronal cells within 24 hrs. Such rapid and neuron-specific gene transduction raises the possibility that A3V vector can be utilized for studies of memory formation in filial imprinting, which occurs during the early postnatal days. A3V injection into the neural tube near the ear vesicle at early embryonic stage resulted in persistent and robust gene expression until E20.5 in the auditory brainstem. We further devised an A3V-mediated tetracycline (Tet) dependent gene expression system as a tool for studying the auditory circuit, consisting of the nucleus magnocellularis (NM) and nucleus laminaris (NL), that primarily computes interaural time differences (ITDs). Using this Tet system, we can transduce NM neurons without affecting NL neurons. Thus, the A3V technology complements current gene transfer techniques in chicken studies and will contribute to better understanding of the functional organization of neural circuits.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23144948/?tool=EBI
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AT yasutotanabe avianadenoassociatedvirusvectorefficientlytransducesneuronsintheembryonicandpostembryonicchickenbrain
AT daiwatanabe avianadenoassociatedvirusvectorefficientlytransducesneuronsintheembryonicandpostembryonicchickenbrain
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