野生小鼠来源1号染色体替换系小鼠的生长表型与血液生化检测
作者:
基金项目:

国家自然科学基金(编号:31171199);上海市创新行动实验动物研究项目(编号:11140900200, 13140900300);中央高校基本科研业务费专项资金,东华大学“励志计划”(B201308)。


Detection of growth phenotype and blood biochemical parameters of wild type-derived chromosome 1 substitution mouse strain
Author:
  • 摘要
  • | |
  • 访问统计
  • |
  • 参考文献 [23]
  • | | | |
  • 文章评论
    摘要:

    目的 分析野生小鼠来源1号染色体替换系小鼠群体的生长表型与血液生化指标,探讨替换系群体的QTL定位潜力。方法 以染色体替换系近交后代小鼠为研究对象,测定其体重、体长、尾长、血液生化、内脏器官重量等表型数据,统计其与C57BL/6差异显著性。结果 发现替换系小鼠在多个指标上与C57BL/6具差异有显著性。不同发育时期的外部表型上与C57BL/6相比,体重具显著差异的是B6-Chr1KM等6个品系,体长具显著差异的是B6-Chr1KM等5个品系,尾长具显著差异的是B6-Chr1KM等9个品系;部分品系在肝、脾、肾脏和脑部重量上存在与C57BL/6的显著差异;生化指标上,丙氨酸氨基转移酶B6-Chr1CM雌鼠显著偏高,碱性磷酸酶B6-Chr1HZ雌鼠显著偏高、B6-Chr1KM雄鼠显著偏低,总胆红素B6-Chr1CM雄鼠、B6-Chr1SMX雄鼠和B6-Chr1HZ雄鼠显著偏高,甘油三酯B6-Chr1SMX雄鼠显著偏高,总胆固醇B6-Chr1TW雄鼠显著偏高。结论 培育的野生小鼠来源的1号染色体替换系群体在部分表型上与C57BL/6差异有显著性,具备作为QTL定位的遗传资源潜力。

    Abstract:

    Objective To analyze the growth phenotype and blood biochemical parameters of chromosome 1 substitution mouse strain(CSS1), and investigate their potential of QTL mapping. Methods Body weight, body length, tail length, organ weight of the CCS1 mice were measured at different days to create a growth curve while blood biochemical indexes were measured at about the 80th day. Results The CCS1 mice were different from C57BL/6 mice in several indexes. Compared with the C57BL/6 mice during different developmental stages, six strains including B6-Chr1KM mice were significantly different in body weight. There were five strains including B6-Chr1CM mice significantly different with C57BL/6 mice in body length, and all of the CSS1 mice were significantly different from C57BL/6 mice in tail length. Part of CCS1 mice were significantly different from C57BL/6 mice in the weight of liver, spleen, kidney and brain. The ALT of female B6-Chr1CM mice was significantly higher than that in the C57BL/6 mice. The ALP of female B6-Chr1HZ mice was significantly higher than that in the male C57BL/6 and B6-Chr1KM mice, and was significantly lower than that in the C57BL/6 mice. The TB of male B6-Chr1CM, B6-Chr1SMX and B6-Chr1HZ mice was significantly higher than that of the C57BL/6 mice. The TG of male B6-Chr1SMX mice and male B6-Chr1TW mice was significantly higher than that in the C57BL/6 mice. Conclusions The phenotype of Chr1 CSS mice is quite different from commonly used inbred strain C57BL/6 mice. CCS1 mice show great potential in QTL mapping for their characteristic growth phenotype and blood biochemical indexes.

    参考文献
    [1] O'Brien T, Woychik R. Our small relative [J]. Nat Genet, 2003, 33: 3-4.
    [2] Laurie CC, Nickerson DA, Anderson AD, et al. Linkage disequilibrium in wild mice [J]. PLoS Genet, 2007, 3(8): e144.
    [3] Guenet JL, Bonhomme F. Wild mice: An ever-increasing contribution to a popular mammalian model [J]. Trends Genet, 2003, 19(1): 24-31.
    [4] Wade CM, Kulbokas EJ, Kirby AW, et al. The mosaic structure of variation in the laboratory mouse genome [J]. Nature, 2002, 420: 574-578.
    [5] Nadeau JH, Singer JB, Matin A, et al. Analysing complex genetic traits with chromosome substitution strains [J]. Nat Genet, 2000, 24(3): 221-225.
    [6] Matin A, Collin GB, Asada Y, et al. Susceptibility to testicular germ-cell tumours in a 129.MOLF-Chr 19 chromosome substitution strain [J]. Nat Genet, 1999, 23: 237-240.
    [7] Cowley AW Jr, Roman RJ, Kaldunsk ML, et al. Brown Norway chromosome 13 confers protection from high salt to consomic Dahl S rat [J]. Hypertension, 2001, 37(2): 456-461.
    [8] Singer JB, Hill AE, Burrage LC, et al. Genetic dissection of complex traits with chromosome substitution strains of mice [J]. Science, 2004, 304(5669): 445-448.
    [9] Shao H, Burrage LC, Sinasac DS, et al. Genetics architecture of complex traits: large phenotypic effects and pervasive epistasis [J]. Proc Natl Acad Sci, 2008, 105(50): 19910-19914.
    [10] Takada T, Mita A, Maeno A, et al. Mouse inter-subspecific consomic strains for genetic dissection of quantitative complex traits [J]. Genome Res, 2008, 18(3): 500-508.
    [11] Gregorova S, Divina P, Storchova R, et al. Mouse consomic strains: exploiting genetic divergence between Mus m. musculus and Mus m. domesticus subspecies [J]. Genome Res, 2008, 18(3): 509-515.
    [12] Singer JB, Hill AE, Nadeau JH, et al. Mapping quantitative trait loci for anxiety in chromosome substitution strains of mice [J]. Genetics, 2005, 169(2): 855-862.
    [13] Xiao J, Liang Y, Li K, et al. A novel strategy for genetic dissection of complex traits: the population of specific chromosome substitution strains from laboratory and wild mice [J]. Mamm Genome, 2010, 21(7-8): 370-376.
    [14] Salcedo T, Geraldes A, Nachman MW. Nucleotide variation in wild and inbred mice [J]. Genetics, 2007, 177(4): 2277-2291.
    [15] Mott R, Flint J. Prospects for complex trait analysis in the mouse [J]. Mamm Genome, 2008, 19(5): 306-308.
    [16] Conlon I, Raff M. Size control in animal development [J]. Cell, 1999, 96(2): 235-244.
    [17] Zhou Y, Liang Y, Li K, et al, The phenotypic distribution of quantitative traits in a wild mouse F1 population [J]. Mamm Genome, 2012, 23(3-4): 232-240.
    [18] Champy MF, Selloum M, Zeitler V, et al, Genetic background determines metabolic phenotypes in the mouse [J]. Mamm Genome, 2008, 19(5): 318-331.
    [19] http:www.informatics.jax.org
    [20] 管彤, 张静姝, 李大鸣, et al. TW近交系小鼠的血液生化及毛色基因检测 [J]. 中国比较医学杂志, 2012, 22(4): 39-42
    [21] 张婷婷, 仝莉, 肖君华, 等. 特异区段替换小鼠性发育表型的研究 [J]. 中国实验动物学报, 2013, 21(2): 1-7
    [22] Peters LL, Robledo RF, Bult CJ, et al. The mouse as a model for human biology: a resource guide for complex trait analysis [J]. Nat Rev Genet, 2007, 8: 58-69
    [23] Brown SD, Hancock JM, Gates H. Understanding mammalian genetic systems: the challenge of phenotyping in the mouse [J]. PLoS Genet, 2006, 2(8): 1131-1137.
    相似文献
    引证文献
    网友评论
    网友评论
    分享到微博
    发 布
引用本文

高遄,徐伟,徐福意,张耀奇,赵莹,赵丽亚,周宇荀,李凯,肖君华.野生小鼠来源1号染色体替换系小鼠的生长表型与血液生化检测[J].中国实验动物学报,2015,23(3):233~238.

复制
分享
文章指标
  • 点击次数:1834
  • 下载次数: 1450
  • HTML阅读次数: 0
  • 引用次数: 0
历史
  • 收稿日期:2014-12-08
  • 在线发布日期: 2015-06-30
文章二维码
防诈骗提示!请勿点击不明链接或添加个人微信。编辑部所有邮箱后缀均为@cnilas.org
关闭