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FVB/NJ小鼠基因组的测序与特征分析。

Sequencing and characterization of the FVB/NJ mouse genome.

作者信息

Wong Kim, Bumpstead Suzannah, Van Der Weyden Louise, Reinholdt Laura G, Wilming Laurens G, Adams David J, Keane Thomas M

出版信息

Genome Biol. 2012 Aug 23;13(8):R72. doi: 10.1186/gb-2012-13-8-r72.

Abstract

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.

摘要

背景

FVB/NJ小鼠品系起源于1935年在美国国立卫生研究院建立的远交瑞士小鼠群体。从该来源获得的小鼠针对对二磷酸组胺的敏感性和弗瑞德白血病病毒B株进行了选择性育种。这导致了FVB/N近交系的建立,该近交系随后被引入杰克逊实验室并命名为FVB/NJ。FVB/NJ小鼠具有几个独特的特征,如原核形态大、繁殖性能旺盛以及产仔数始终较多,这使得它在转基因品系生产和通用方面非常理想。

结果

使用下一代测序技术,我们对FVB/NJ基因组进行了约50倍覆盖率的测序,并相对于参考C57BL/6J基因组生成了单核苷酸多态性、小插入/缺失多态性和结构变异的综合目录。我们检查了先前在10号染色体上鉴定出的动脉粥样硬化易感性数量性状位点,并确定了几个先前未知的候选因果变异。

结论

FVB/NJ基因组的测序以及该目录的生成使FVB/NJ中已知变异位点的数量增加了四倍,并将有助于加速鉴定导致在这个广泛使用的品系中观察到的表型的精确分子变异。

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