期刊文献+

鉴定清道夫受体BI基因敲除突变小鼠的新方法 被引量:1

A novel method for genotyping scavenger receptor BI gene knockout mice
原文传递
导出
摘要 目的建立一种清道夫受体BI(SR-BI)基因敲除突变小鼠基因型的鉴定方法。方法参照碱基淬灭探针技术原理,设计鉴定野生型和突变型SR-BI基因的引物探针。反应体系经PCR扩增后,利用融解曲线功能判断小鼠基因型。结果新方法可在1h内完成基因型分析。野生型和突变型纯合子小鼠分别在(53.25±0.81)℃及(62.25±0.31)℃处出现单个融解谷;而杂合子小鼠在两处均出现融解谷。结论新方法简单、快速、准确,适用于鉴别SR-BI基因敲除突变小鼠的基因型。 Objective To establish a practical method for determining the genotype of scavenger receptor BI(SR-BI)gene knockout mice.Methods Primers and probes were designed according to the base-quenched probe technique and the targeted SR-BI genotypes were analyzed using melting curve.Results The analysis for genotyping could be completed with the tecnigue mentioned above within 1 h.Single melting valley appeared at the melting temperatures of (62.25±0.31)℃ and (53.25±0.81)℃ for the rats with homozygous and wild-type,respectively.The rats with heterozygous showed two melting valleys.Conclusion The procedure of this novel method is accurate,simple and quicke,which is suitable for genotyping the SR-BI gene knockout mice.
出处 《江苏医药》 CAS CSCD 北大核心 2011年第3期258-260,共3页 Jiangsu Medical Journal
基金 江苏省自然科学基金(BK2008140) 常州市卫生局重大招标项目资助课题(ZD200709)
关键词 清道夫受体BI 基因敲除 Scavenger receptor BI Gene knockout
  • 相关文献

参考文献10

  • 1Acton S, Rigotti A,Landsehulz KT, et al. Identification of scavenger receptor SR-BI as a high density lipoprotein receptor[J]. Science, 1996,271(5248) : 518 -520.
  • 2Huby T, Doucet C, Dachet C,et al. Knockdown expression and hepatic deficiency reveal an atheroprotective role for SR-BI in liver and peripheral tissues[J].J Clin Invest, 2006, 116(10): 2767-2776.
  • 3Rigotti A, Trigatti BL, Penman M, et al. A targeted mutation in the murine gene encoding the high density lipoprotein (HDL) receptor scavenger receptor class B type I reveals its key role in HDL metabolism[J].Proc Natl Acad Sci USA, 1997,94 (23) : 12610-12615.
  • 4Luo G,Zheng L,Zhang X,et al. Genotyping f single nucleotide polymorphisms using base-quenched probe: a method does not invariably depend on the deoxyguanosine nucleotide [J]. Anal Biochem,2009,386(2) : 161-166.
  • 5张俊,罗光华,郑璐,张晓膺,徐宁.单核苷酸多态性的碱基淬灭探针技术检测方法的建立[J].中华检验医学杂志,2009,32(9):1064-1068. 被引量:12
  • 6Silver DL, Tall AR. The cellular biology of scavenger receptor class B type I[J]. Curr Opin Lipidol, 2001,12 (5):497- 504.
  • 7Matveev S, Uittenbogaard A, van Der Westhuyzen D, et al. Caveolin-1 negatively regulates SR-BI mediated selective uptake of high-density lipoprotein-derived cholesteryl ester[J]. Eur J Biochem,2001,268(21) :5609-5616,.
  • 8Duncan KG, Bailey KR, Kane JP, et al. Human retinal pigment epithelial cells express scavenger receptors BI and BII [J]. Biochem Biophys Res Commun, 2002, 292 (4) : 1017- 1022.
  • 9陈广文,刘喜玲,肖献忠.PCR方法在HSF1基因敲除小鼠基因型分析中的应用[J].中国实验动物学报,2002,10(2):73-76. 被引量:5
  • 10吴振恭,褚汉启,熊浩,韩芳,黄孝文,崔永华.NKCC1基因敲除小鼠的饲养繁殖及其鉴定[J].听力学及言语疾病杂志,2006,14(5):379-380. 被引量:1

二级参考文献22

  • 1熊浩,褚汉启,韩芳,吴振恭,张平,王春芳,崔永华.卡那霉素对三种小鼠耳毒性比较及对血管纹Na-K-2Cl联合转运子1表达的影响[J].中华耳鼻咽喉头颈外科杂志,2006,41(1):43-47. 被引量:6
  • 2熊浩,褚汉启,韩芳,吴振恭,黄孝文,张平,崔永华.C57BL/6J小鼠耳蜗血管纹Na-K-2Cl联合转运子-1的年龄相关性变化[J].听力学及言语疾病杂志,2006,14(2):125-126. 被引量:7
  • 3罗光华,郑璐,张晓膺,许国锋,朱江,牟琴峰,魏江,陈陆俊,张俊,徐宁.ShineRoar探针技术检测单核苷酸多态性[J].中华检验医学杂志,2007,30(6):609-612. 被引量:8
  • 4Brookes AJ. The essence of SNPs. Gene, 1999,234 : 177-186.
  • 5The International HapMap Consortium. The international HapMap project. Nature, 2003,426:789-796.
  • 6Chung WH, Hung SI, Hong HS, et al. Medical genetics: a marker for Stevens-Johnson syndrome. Nature, 2004,428:486.
  • 7Carlson CS, Newman TL, Nickerson DA. SNPing in the human genome. Curr Opin Chem Biol, 2001,5:78-85.
  • 8Zhang R, Zhu Z, Zhu H, et al. SNP Cutter: a comprehensive tool for SNP PCR-RFLP assay design. Nucleic Acids Res, 2005, 33 : W489-492.
  • 9Takatsu K, Yokomaku T, Kurata S, et al. A new approach to SNP genotyping with fluorescently labeled mononucleotides. Nucleic Acids Res, 2004,32 : e60.
  • 10Crockett AO,Wittwer CT. Fluorescein-labeled oligonucleotides for real-time pcr: using the inherent quenching of deoxyguanosine nucleotides. Anal Biochem, 2001,290:89-97.

共引文献15

同被引文献2

引证文献1

二级引证文献2

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