Xu Fuyi, Chao Tianzhu, Liang Yingming, Li Kai, Hu Shixian, Wang Maochun, Zhou Yuxun, Xu Hongyan, Xiao Junhua
College of Chemistry, Chemical Engineering, and Biotechnology, Donghua University, Shanghai 201620, China.
The Laboratory of Genetic Regulators in the Immune System, Xinxiang Medical University, Henan 453003, China.
G3 (Bethesda). 2016 Nov 8;6(11):3571-3580. doi: 10.1534/g3.116.033902.
Mouse resources such as Collaborative Cross, outbred stocks, Hybrid Mouse Diversity Panel, and chromosome substitution strains have been instrumental to many progresses in the studies of complex traits genetics. We have established a population of chromosome 1 (Chr 1) substitution lines (C1SLs) in which donor chromosomes were derived from Chinese wild mice. Genome sequencing of 18 lines of this population showed that Chr 1 had been replaced by the donor chromosome. About 4.5 million unique single nucleotide polymorphisms and indels were discovered on Chr 1, of which 1.3 million were novel. Compared with sequenced classical inbred strains, Chr 1 of each C1SL had fivefold more variants, and more loss of function and potentially regulatory variants. Further haplotype analysis showed that the donor chromosome accumulated more historical recombination events, with the largest haplotype block being only 100 kb, and about 57% of the blocks were <1 kb. Subspecies origin analysis showed that these chromosomes had a mosaic genome structure that dominantly originated from and subspecies, except for the C57BL/6J-Chr1 line from In addition, phenotyping four of these lines on blood biochemistry suggested that there were substantial phenotypic variations among our lines, especially line C57BL/6J-Chr1 and donor strain C57BL/6J. Further gene ontology enrichment revealed that the differentially expressed genes among liver-expressed genes between C57BL/6J and C57BL/6J-Chr1 were enriched in lipid metabolism biological processes. All these characteristics enable C1SLs to be a unique resource for identifying and fine mapping quantitative trait loci on mouse Chr 1, and carrying out systems genetics studies of complex traits.
诸如协作杂交、远交群体、杂交小鼠多样性面板和染色体代换系等小鼠资源,对复杂性状遗传学研究的诸多进展起到了重要作用。我们建立了一个1号染色体(Chr 1)代换系群体(C1SLs),其中供体染色体源自中国野生小鼠。对该群体中18个品系进行基因组测序表明,Chr 1已被供体染色体取代。在Chr 1上发现了约450万个独特的单核苷酸多态性和插入缺失,其中130万个是新发现的。与已测序的经典近交系相比,每个C1SL的Chr 1具有多五倍的变异,以及更多的功能丧失变异和潜在调控变异。进一步的单倍型分析表明,供体染色体积累了更多的历史重组事件,最大的单倍型块仅为100 kb,约57%的块小于1 kb。亚种起源分析表明,这些染色体具有镶嵌基因组结构,主要源自 和 亚种,但C57BL/6J-Chr1品系除外,它来自 。此外,对其中4个品系进行血液生化表型分析表明,我们的品系之间存在显著的表型差异,尤其是C57BL/6J-Chr1品系和供体品系C57BL/6J。进一步的基因本体富集分析表明,C57BL/6J和C57BL/6J-Chr1之间肝脏表达基因中差异表达的基因在脂质代谢生物学过程中富集。所有这些特性使C1SLs成为鉴定和精细定位小鼠Chr 1上数量性状位点以及开展复杂性状系统遗传学研究的独特资源。
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