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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...

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Autores principales: Wong, Kim, Bumpstead, Suzannah, Van Der Weyden, Louise, Reinholdt, Laura G, Wilming, Laurens G, Adams, David J, Keane, Thomas M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
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.
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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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