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Brain selective transgene expression in zebrafish using an NRSE derived motif

Transgenic technologies enable the manipulation and observation of circuits controlling behavior by permitting expression of genetically encoded reporter genes in neurons. Frequently though, neuronal expression is accompanied by transgene expression in non-neuronal tissues, which may preclude key ex...

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Autores principales: Bergeron, Sadie A., Hannan, Markus C., Codore, Hiba, Fero, Kandice, Li, Grace H., Moak, Zachary, Yokogawa, Tohei, Burgess, Harold A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3531662/
https://www.ncbi.nlm.nih.gov/pubmed/23293587
http://dx.doi.org/10.3389/fncir.2012.00110
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author Bergeron, Sadie A.
Hannan, Markus C.
Codore, Hiba
Fero, Kandice
Li, Grace H.
Moak, Zachary
Yokogawa, Tohei
Burgess, Harold A.
author_facet Bergeron, Sadie A.
Hannan, Markus C.
Codore, Hiba
Fero, Kandice
Li, Grace H.
Moak, Zachary
Yokogawa, Tohei
Burgess, Harold A.
author_sort Bergeron, Sadie A.
collection PubMed
description Transgenic technologies enable the manipulation and observation of circuits controlling behavior by permitting expression of genetically encoded reporter genes in neurons. Frequently though, neuronal expression is accompanied by transgene expression in non-neuronal tissues, which may preclude key experimental manipulations, including assessment of the contribution of neurons to behavior by ablation. To better restrict transgene expression to the nervous system in zebrafish larvae, we have used DNA sequences derived from the neuron-restrictive silencing element (NRSE). We find that one such sequence, REx2, when used in conjunction with several basal promoters, robustly suppresses transgene expression in non-neuronal tissues. Both in transient transgenic experiments and in stable enhancer trap lines, suppression is achieved without compromising expression within the nervous system. Furthermore, in REx2 enhancer trap lines non-neuronal expression can be de-repressed by knocking down expression of the NRSE binding protein RE1-silencing transcription factor (Rest). In one line, we show that the resulting pattern of reporter gene expression coincides with that of the adjacent endogenous gene, hapln3. We demonstrate that three common basal promoters are susceptible to the effects of the REx2 element, suggesting that this method may be useful for confining expression from many other promoters to the nervous system. This technique enables neural specific targeting of reporter genes and thus will facilitate the use of transgenic methods to manipulate circuit function in freely behaving larvae.
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spelling pubmed-35316622013-01-04 Brain selective transgene expression in zebrafish using an NRSE derived motif Bergeron, Sadie A. Hannan, Markus C. Codore, Hiba Fero, Kandice Li, Grace H. Moak, Zachary Yokogawa, Tohei Burgess, Harold A. Front Neural Circuits Neuroscience Transgenic technologies enable the manipulation and observation of circuits controlling behavior by permitting expression of genetically encoded reporter genes in neurons. Frequently though, neuronal expression is accompanied by transgene expression in non-neuronal tissues, which may preclude key experimental manipulations, including assessment of the contribution of neurons to behavior by ablation. To better restrict transgene expression to the nervous system in zebrafish larvae, we have used DNA sequences derived from the neuron-restrictive silencing element (NRSE). We find that one such sequence, REx2, when used in conjunction with several basal promoters, robustly suppresses transgene expression in non-neuronal tissues. Both in transient transgenic experiments and in stable enhancer trap lines, suppression is achieved without compromising expression within the nervous system. Furthermore, in REx2 enhancer trap lines non-neuronal expression can be de-repressed by knocking down expression of the NRSE binding protein RE1-silencing transcription factor (Rest). In one line, we show that the resulting pattern of reporter gene expression coincides with that of the adjacent endogenous gene, hapln3. We demonstrate that three common basal promoters are susceptible to the effects of the REx2 element, suggesting that this method may be useful for confining expression from many other promoters to the nervous system. This technique enables neural specific targeting of reporter genes and thus will facilitate the use of transgenic methods to manipulate circuit function in freely behaving larvae. Frontiers Media S.A. 2012-12-28 /pmc/articles/PMC3531662/ /pubmed/23293587 http://dx.doi.org/10.3389/fncir.2012.00110 Text en Copyright © 2012 Bergeron, Hannan, Codore, Fero, Li, Moak, Yokogawa and Burgess. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Neuroscience
Bergeron, Sadie A.
Hannan, Markus C.
Codore, Hiba
Fero, Kandice
Li, Grace H.
Moak, Zachary
Yokogawa, Tohei
Burgess, Harold A.
Brain selective transgene expression in zebrafish using an NRSE derived motif
title Brain selective transgene expression in zebrafish using an NRSE derived motif
title_full Brain selective transgene expression in zebrafish using an NRSE derived motif
title_fullStr Brain selective transgene expression in zebrafish using an NRSE derived motif
title_full_unstemmed Brain selective transgene expression in zebrafish using an NRSE derived motif
title_short Brain selective transgene expression in zebrafish using an NRSE derived motif
title_sort brain selective transgene expression in zebrafish using an nrse derived motif
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3531662/
https://www.ncbi.nlm.nih.gov/pubmed/23293587
http://dx.doi.org/10.3389/fncir.2012.00110
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