期刊文献+

S100A16基因敲除小鼠模型的构建与鉴定 被引量:2

Establishment and identification of S100A16 gene knockout mouse model
下载PDF
导出
摘要 目的:S100A16在肥胖以及多种恶性肿瘤发生发展中发挥了重要作用,本研究拟构建S100A16基因敲除小鼠模型。方法:利用基因表达调控系统(即Cre/lox P系统)构建全身敲除小鼠。采用聚合酶链式反应(PCR)鉴定小鼠的基因型,采用实时定量PCR(QRT-PCR)、Western blot方法验证其转录及翻译水平的表达。结果:成功建立了S100A16全身敲除小鼠模型,基因敲除杂合子小鼠成功饲养繁殖,目前为止未出现纯合子小鼠。S100A16敲除小鼠主要代谢器官,如脂肪、肌肉、肝脏中S100A16蛋白表达量显著下降。结论:S100A16基因敲除小鼠模型的构建为研究肥胖及胰岛素抵抗中的作用及机制提供了动物模型。 Objective:To establish the S100A16 gene knockout mouse model,which can be used for the study on its biologic func- tion. Methods:To establish the S100A16 gene knockout mouse model via Cre/loxP system. PCR was used to identify the genotype of the offspring,the expression level of S100A16 mRNA was detected by qRT-PCR,and expression of S100A16 protein was detected by Western blot. Results:S100A16 gene knockout mouse model has been successfully established, tIeterozygous mice were successfully bred and reproduced. So far,gene knockout homozygous mice were not found. Conclusion:The S100A16 mouse could be a useful model for the researches on its function, especially in obesity and insulin resistance.
出处 《南京医科大学学报(自然科学版)》 CSCD 北大核心 2017年第5期549-553,共5页 Journal of Nanjing Medical University(Natural Sciences)
基金 国家自然科学基金(81270952)
关键词 S100A16 基因敲除 动物模型 S 100A 16 gene knockout animal model
  • 相关文献

参考文献1

二级参考文献17

  • 1Paterson JM, Morton NM, Fievet C, et al. Metabolic syndrome without obesity: Hepatic overexpression of 11betahydroxysteroid dehydrogenase type 1 in trans genic mice [J]. Proc Natl Acad Sci USA, 2004,101(18) : 7088-7093.
  • 2Herr CE, Zur Nieden A, Kopka I, et al. Assessment of somatic complaints in environmental health [J]. Int J Hyg Environ Health, 2009 ,212(1): 27-36.
  • 3Heizmann CWo The multifunctional S 100 protein family [J]. Methods Mol Bioi, 2002, 172 ( 1) : 69-80.
  • 4Heizmann CW, Fritz G, Schafer BW. S 100 proteins: structure,functions and pathology [J]. Front Biosci,2002,7: d1356-1368.
  • 5Sturchler E,Cox JA,Durussel I,et al. S100A16,a novel calcium-binding protein of the EF-hand superfamily[J]. J Bioi Chern, 2006,281 (50): 38905-38917.
  • 6Marenholz I, Heizmann CW, Fritz G. S 100 proteins in mouse and man: from evolution to function and pathology (including an update of the nomenclature) [J]. Biochem Biophys Res Commun,2004,322(4): 1111-1122.
  • 7Zhang R,Zhu W,Du X,et al. S100A16 mediation of weight gain attenuation induced by dietary calcium [J]. Metabolism, 2012, 61 (2) : 157-163.
  • 8Liu Y ,Zhang R,Xin J ,et al. Identification of S100A16 as a novel adipogenesis promoting factor in 3T3-L1 cells[J]. Endocrinology ,2011,152(3) :903-911.
  • 9Yao R, Lopez- Beltran A, Maclennan GT, et al. Expression of S100 protein family members in the pathogenesis of bladder tumors[J]. Anticancer Res, 2007 , 27(5A): 3051- 3058.
  • 10Gaggini M, Morelli M, Buzzigoli E, et al. Non-alcoholic fatty liver disease (NAFLD) and its connection with insulin resistance, dyslipidemia, atherosclerosis and coronary heart disease[J]. Nutrients ,2013,5(5): 1544-1560.

同被引文献7

引证文献2

二级引证文献7

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部