Cargando…
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...
Autores principales: | , , , , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1782480752464625664 |
---|---|
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. |
format | Online Article Text |
id | pubmed-4091307 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT harrisjuliea anatomicalcharacterizationofcredrivermiceforneuralcircuitmappingandmanipulation AT hirokawakarlae anatomicalcharacterizationofcredrivermiceforneuralcircuitmappingandmanipulation AT sorensenstacia anatomicalcharacterizationofcredrivermiceforneuralcircuitmappingandmanipulation AT guhong anatomicalcharacterizationofcredrivermiceforneuralcircuitmappingandmanipulation AT millsmaya anatomicalcharacterizationofcredrivermiceforneuralcircuitmappingandmanipulation AT nglydial anatomicalcharacterizationofcredrivermiceforneuralcircuitmappingandmanipulation AT bohnphillip anatomicalcharacterizationofcredrivermiceforneuralcircuitmappingandmanipulation AT mortrudmarty anatomicalcharacterizationofcredrivermiceforneuralcircuitmappingandmanipulation AT ouellettebenjamin anatomicalcharacterizationofcredrivermiceforneuralcircuitmappingandmanipulation AT kidneyjolene anatomicalcharacterizationofcredrivermiceforneuralcircuitmappingandmanipulation AT smithkimberlya anatomicalcharacterizationofcredrivermiceforneuralcircuitmappingandmanipulation AT dangchinh anatomicalcharacterizationofcredrivermiceforneuralcircuitmappingandmanipulation AT sunkinsusan anatomicalcharacterizationofcredrivermiceforneuralcircuitmappingandmanipulation AT bernardamy anatomicalcharacterizationofcredrivermiceforneuralcircuitmappingandmanipulation AT ohseungwook anatomicalcharacterizationofcredrivermiceforneuralcircuitmappingandmanipulation AT madisenlinda anatomicalcharacterizationofcredrivermiceforneuralcircuitmappingandmanipulation AT zenghongkui anatomicalcharacterizationofcredrivermiceforneuralcircuitmappingandmanipulation |