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Molecular Characterization of Mutant Mouse Strains Generated from the EUCOMM/KOMP-CSD ES Cell Resource
The Sanger Mouse Genetics Project generates knockout mice strains using the EUCOMM/KOMP-CSD embryonic stem (ES) cell collection and characterizes the consequences of the mutations using a high-throughput primary phenotyping screen. Upon achieving germline transmission, new strains are subject to a p...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3745610/ https://www.ncbi.nlm.nih.gov/pubmed/23912999 http://dx.doi.org/10.1007/s00335-013-9467-x |
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author | Ryder, Edward Gleeson, Diane Sethi, Debarati Vyas, Sapna Miklejewska, Evelina Dalvi, Priya Habib, Bishoy Cook, Ross Hardy, Matthew Jhaveri, Kalpesh Bottomley, Joanna Wardle-Jones, Hannah Bussell, James N. Houghton, Richard Salisbury, Jennifer Skarnes, William C. Ramirez-Solis, Ramiro |
author_facet | Ryder, Edward Gleeson, Diane Sethi, Debarati Vyas, Sapna Miklejewska, Evelina Dalvi, Priya Habib, Bishoy Cook, Ross Hardy, Matthew Jhaveri, Kalpesh Bottomley, Joanna Wardle-Jones, Hannah Bussell, James N. Houghton, Richard Salisbury, Jennifer Skarnes, William C. Ramirez-Solis, Ramiro |
author_sort | Ryder, Edward |
collection | PubMed |
description | The Sanger Mouse Genetics Project generates knockout mice strains using the EUCOMM/KOMP-CSD embryonic stem (ES) cell collection and characterizes the consequences of the mutations using a high-throughput primary phenotyping screen. Upon achieving germline transmission, new strains are subject to a panel of quality control (QC) PCR- and qPCR-based assays to confirm the correct targeting, cassette structure, and the presence of the 3′ LoxP site (required for the potential conditionality of the allele). We report that over 86 % of the 731 strains studied showed the correct targeting and cassette structure, of which 97 % retained the 3′ LoxP site. We discuss the characteristics of the lines that failed QC and postulate that the majority of these may be due to mixed ES cell populations which were not detectable with the original screening techniques employed when creating the ES cell resource. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00335-013-9467-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-3745610 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-37456102013-08-20 Molecular Characterization of Mutant Mouse Strains Generated from the EUCOMM/KOMP-CSD ES Cell Resource Ryder, Edward Gleeson, Diane Sethi, Debarati Vyas, Sapna Miklejewska, Evelina Dalvi, Priya Habib, Bishoy Cook, Ross Hardy, Matthew Jhaveri, Kalpesh Bottomley, Joanna Wardle-Jones, Hannah Bussell, James N. Houghton, Richard Salisbury, Jennifer Skarnes, William C. Ramirez-Solis, Ramiro Mamm Genome Article The Sanger Mouse Genetics Project generates knockout mice strains using the EUCOMM/KOMP-CSD embryonic stem (ES) cell collection and characterizes the consequences of the mutations using a high-throughput primary phenotyping screen. Upon achieving germline transmission, new strains are subject to a panel of quality control (QC) PCR- and qPCR-based assays to confirm the correct targeting, cassette structure, and the presence of the 3′ LoxP site (required for the potential conditionality of the allele). We report that over 86 % of the 731 strains studied showed the correct targeting and cassette structure, of which 97 % retained the 3′ LoxP site. We discuss the characteristics of the lines that failed QC and postulate that the majority of these may be due to mixed ES cell populations which were not detectable with the original screening techniques employed when creating the ES cell resource. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00335-013-9467-x) contains supplementary material, which is available to authorized users. Springer US 2013-08-04 2013 /pmc/articles/PMC3745610/ /pubmed/23912999 http://dx.doi.org/10.1007/s00335-013-9467-x Text en © The Author(s) 2013 https://creativecommons.org/licenses/by/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Article Ryder, Edward Gleeson, Diane Sethi, Debarati Vyas, Sapna Miklejewska, Evelina Dalvi, Priya Habib, Bishoy Cook, Ross Hardy, Matthew Jhaveri, Kalpesh Bottomley, Joanna Wardle-Jones, Hannah Bussell, James N. Houghton, Richard Salisbury, Jennifer Skarnes, William C. Ramirez-Solis, Ramiro Molecular Characterization of Mutant Mouse Strains Generated from the EUCOMM/KOMP-CSD ES Cell Resource |
title | Molecular Characterization of Mutant Mouse Strains Generated from the EUCOMM/KOMP-CSD ES Cell Resource |
title_full | Molecular Characterization of Mutant Mouse Strains Generated from the EUCOMM/KOMP-CSD ES Cell Resource |
title_fullStr | Molecular Characterization of Mutant Mouse Strains Generated from the EUCOMM/KOMP-CSD ES Cell Resource |
title_full_unstemmed | Molecular Characterization of Mutant Mouse Strains Generated from the EUCOMM/KOMP-CSD ES Cell Resource |
title_short | Molecular Characterization of Mutant Mouse Strains Generated from the EUCOMM/KOMP-CSD ES Cell Resource |
title_sort | molecular characterization of mutant mouse strains generated from the eucomm/komp-csd es cell resource |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3745610/ https://www.ncbi.nlm.nih.gov/pubmed/23912999 http://dx.doi.org/10.1007/s00335-013-9467-x |
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