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Anatomical characterization of Cre driver mice for neural circuit mapping and manipulation

Significant advances in circuit-level analyses of the brain require tools that allow for labeling, modulation of gene expression, and monitoring and manipulation of cellular activity in specific cell types and/or anatomical regions. Large-scale projects and individual laboratories have produced hund...

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Autores principales: Harris, Julie A., Hirokawa, Karla E., Sorensen, Staci A., Gu, Hong, Mills, Maya, Ng, Lydia L., Bohn, Phillip, Mortrud, Marty, Ouellette, Benjamin, Kidney, Jolene, Smith, Kimberly A., Dang, Chinh, Sunkin, Susan, Bernard, Amy, Oh, Seung Wook, Madisen, Linda, Zeng, Hongkui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4091307/
https://www.ncbi.nlm.nih.gov/pubmed/25071457
http://dx.doi.org/10.3389/fncir.2014.00076
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author Harris, Julie A.
Hirokawa, Karla E.
Sorensen, Staci A.
Gu, Hong
Mills, Maya
Ng, Lydia L.
Bohn, Phillip
Mortrud, Marty
Ouellette, Benjamin
Kidney, Jolene
Smith, Kimberly A.
Dang, Chinh
Sunkin, Susan
Bernard, Amy
Oh, Seung Wook
Madisen, Linda
Zeng, Hongkui
author_facet Harris, Julie A.
Hirokawa, Karla E.
Sorensen, Staci A.
Gu, Hong
Mills, Maya
Ng, Lydia L.
Bohn, Phillip
Mortrud, Marty
Ouellette, Benjamin
Kidney, Jolene
Smith, Kimberly A.
Dang, Chinh
Sunkin, Susan
Bernard, Amy
Oh, Seung Wook
Madisen, Linda
Zeng, Hongkui
author_sort Harris, Julie A.
collection PubMed
description Significant advances in circuit-level analyses of the brain require tools that allow for labeling, modulation of gene expression, and monitoring and manipulation of cellular activity in specific cell types and/or anatomical regions. Large-scale projects and individual laboratories have produced hundreds of gene-specific promoter-driven Cre mouse lines invaluable for enabling genetic access to subpopulations of cells in the brain. However, the potential utility of each line may not be fully realized without systematic whole brain characterization of transgene expression patterns. We established a high-throughput in situ hybridization (ISH), imaging and data processing pipeline to describe whole brain gene expression patterns in Cre driver mice. Currently, anatomical data from over 100 Cre driver lines are publicly available via the Allen Institute's Transgenic Characterization database, which can be used to assist researchers in choosing the appropriate Cre drivers for functional, molecular, or connectional studies of different regions and/or cell types in the brain.
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spelling pubmed-40913072014-07-28 Anatomical characterization of Cre driver mice for neural circuit mapping and manipulation Harris, Julie A. Hirokawa, Karla E. Sorensen, Staci A. Gu, Hong Mills, Maya Ng, Lydia L. Bohn, Phillip Mortrud, Marty Ouellette, Benjamin Kidney, Jolene Smith, Kimberly A. Dang, Chinh Sunkin, Susan Bernard, Amy Oh, Seung Wook Madisen, Linda Zeng, Hongkui Front Neural Circuits Neuroscience Significant advances in circuit-level analyses of the brain require tools that allow for labeling, modulation of gene expression, and monitoring and manipulation of cellular activity in specific cell types and/or anatomical regions. Large-scale projects and individual laboratories have produced hundreds of gene-specific promoter-driven Cre mouse lines invaluable for enabling genetic access to subpopulations of cells in the brain. However, the potential utility of each line may not be fully realized without systematic whole brain characterization of transgene expression patterns. We established a high-throughput in situ hybridization (ISH), imaging and data processing pipeline to describe whole brain gene expression patterns in Cre driver mice. Currently, anatomical data from over 100 Cre driver lines are publicly available via the Allen Institute's Transgenic Characterization database, which can be used to assist researchers in choosing the appropriate Cre drivers for functional, molecular, or connectional studies of different regions and/or cell types in the brain. Frontiers Media S.A. 2014-07-10 /pmc/articles/PMC4091307/ /pubmed/25071457 http://dx.doi.org/10.3389/fncir.2014.00076 Text en Copyright © 2014 Harris, Hirokawa, Sorensen, Gu, Mills, Ng, Bohn, Mortrud, Ouellette, Kidney, Smith, Dang, Sunkin, Bernard, Oh, Madisen and Zeng. http://creativecommons.org/licenses/by/3.0/ 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 Neuroscience
Harris, Julie A.
Hirokawa, Karla E.
Sorensen, Staci A.
Gu, Hong
Mills, Maya
Ng, Lydia L.
Bohn, Phillip
Mortrud, Marty
Ouellette, Benjamin
Kidney, Jolene
Smith, Kimberly A.
Dang, Chinh
Sunkin, Susan
Bernard, Amy
Oh, Seung Wook
Madisen, Linda
Zeng, Hongkui
Anatomical characterization of Cre driver mice for neural circuit mapping and manipulation
title Anatomical characterization of Cre driver mice for neural circuit mapping and manipulation
title_full Anatomical characterization of Cre driver mice for neural circuit mapping and manipulation
title_fullStr Anatomical characterization of Cre driver mice for neural circuit mapping and manipulation
title_full_unstemmed Anatomical characterization of Cre driver mice for neural circuit mapping and manipulation
title_short Anatomical characterization of Cre driver mice for neural circuit mapping and manipulation
title_sort anatomical characterization of cre driver mice for neural circuit mapping and manipulation
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4091307/
https://www.ncbi.nlm.nih.gov/pubmed/25071457
http://dx.doi.org/10.3389/fncir.2014.00076
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