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Sequencing and characterization of the FVB/NJ mouse genome
BACKGROUND: The FVB/NJ mouse strain has its origins in a colony of outbred Swiss mice established in 1935 at the National Institutes of Health. Mice derived from this source were selectively bred for sensitivity to histamine diphosphate and the B strain of Friend leukemia virus. This led to the esta...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3491372/ https://www.ncbi.nlm.nih.gov/pubmed/22916792 http://dx.doi.org/10.1186/gb-2012-13-8-r72 |
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author | Wong, Kim Bumpstead, Suzannah Van Der Weyden, Louise Reinholdt, Laura G Wilming, Laurens G Adams, David J Keane, Thomas M |
author_facet | Wong, Kim Bumpstead, Suzannah Van Der Weyden, Louise Reinholdt, Laura G Wilming, Laurens G Adams, David J Keane, Thomas M |
author_sort | Wong, Kim |
collection | PubMed |
description | BACKGROUND: The FVB/NJ mouse strain has its origins in a colony of outbred Swiss mice established in 1935 at the National Institutes of Health. Mice derived from this source were selectively bred for sensitivity to histamine diphosphate and the B strain of Friend leukemia virus. This led to the establishment of the FVB/N inbred strain, which was subsequently imported to the Jackson Laboratory and designated FVB/NJ. The FVB/NJ mouse has several distinct characteristics, such as large pronuclear morphology, vigorous reproductive performance, and consistently large litters that make it highly desirable for transgenic strain production and general purpose use. RESULTS: Using next-generation sequencing technology, we have sequenced the genome of FVB/NJ to approximately 50-fold coverage, and have generated a comprehensive catalog of single nucleotide polymorphisms, small insertion/deletion polymorphisms, and structural variants, relative to the reference C57BL/6J genome. We have examined a previously identified quantitative trait locus for atherosclerosis susceptibility on chromosome 10 and identify several previously unknown candidate causal variants. CONCLUSION: The sequencing of the FVB/NJ genome and generation of this catalog has increased the number of known variant sites in FVB/NJ by a factor of four, and will help accelerate the identification of the precise molecular variants that are responsible for phenotypes observed in this widely used strain. |
format | Online Article Text |
id | pubmed-3491372 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34913722012-11-07 Sequencing and characterization of the FVB/NJ mouse genome Wong, Kim Bumpstead, Suzannah Van Der Weyden, Louise Reinholdt, Laura G Wilming, Laurens G Adams, David J Keane, Thomas M Genome Biol Research BACKGROUND: The FVB/NJ mouse strain has its origins in a colony of outbred Swiss mice established in 1935 at the National Institutes of Health. Mice derived from this source were selectively bred for sensitivity to histamine diphosphate and the B strain of Friend leukemia virus. This led to the establishment of the FVB/N inbred strain, which was subsequently imported to the Jackson Laboratory and designated FVB/NJ. The FVB/NJ mouse has several distinct characteristics, such as large pronuclear morphology, vigorous reproductive performance, and consistently large litters that make it highly desirable for transgenic strain production and general purpose use. RESULTS: Using next-generation sequencing technology, we have sequenced the genome of FVB/NJ to approximately 50-fold coverage, and have generated a comprehensive catalog of single nucleotide polymorphisms, small insertion/deletion polymorphisms, and structural variants, relative to the reference C57BL/6J genome. We have examined a previously identified quantitative trait locus for atherosclerosis susceptibility on chromosome 10 and identify several previously unknown candidate causal variants. CONCLUSION: The sequencing of the FVB/NJ genome and generation of this catalog has increased the number of known variant sites in FVB/NJ by a factor of four, and will help accelerate the identification of the precise molecular variants that are responsible for phenotypes observed in this widely used strain. BioMed Central 2012 2012-08-23 /pmc/articles/PMC3491372/ /pubmed/22916792 http://dx.doi.org/10.1186/gb-2012-13-8-r72 Text en Copyright ©2012 Wong et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Wong, Kim Bumpstead, Suzannah Van Der Weyden, Louise Reinholdt, Laura G Wilming, Laurens G Adams, David J Keane, Thomas M Sequencing and characterization of the FVB/NJ mouse genome |
title | Sequencing and characterization of the FVB/NJ mouse genome |
title_full | Sequencing and characterization of the FVB/NJ mouse genome |
title_fullStr | Sequencing and characterization of the FVB/NJ mouse genome |
title_full_unstemmed | Sequencing and characterization of the FVB/NJ mouse genome |
title_short | Sequencing and characterization of the FVB/NJ mouse genome |
title_sort | sequencing and characterization of the fvb/nj mouse genome |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3491372/ https://www.ncbi.nlm.nih.gov/pubmed/22916792 http://dx.doi.org/10.1186/gb-2012-13-8-r72 |
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