首页> 美国卫生研究院文献>Journal of Visualized Experiments : JoVE >Telomerase Activity in the Various Regions of Mouse Brain: Non-Radioactive Telomerase Repeat Amplification Protocol (TRAP) Assay
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Telomerase Activity in the Various Regions of Mouse Brain: Non-Radioactive Telomerase Repeat Amplification Protocol (TRAP) Assay

机译:小鼠大脑各个区域的端粒酶活性:非放射性端粒酶重复扩增协议(TRAP)分析

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摘要

Telomerase, a ribonucleoprotein, is responsible for maintaining the telomere length and therefore promoting genomic integrity, proliferation, and lifespan. In addition, telomerase protects the mitochondria from oxidative stress and confers resistance to apoptosis, suggesting its possible importance for the surviving of non-mitotic, highly active cells such as neurons. We previously demonstrated the ability of novel telomerase activators to increase telomerase activity and expression in the various mouse brain regions and to protect motor neurons cells from oxidative stress. These results strengthen the notion that telomerase is involved in the protection of neurons from various lesions. To underline the role of telomerase in the brain, we here compare the activity of telomerase in male and female mouse brain and its dependence on age. TRAP assay is a standard method for detecting telomerase activity in various tissues or cell lines. Here we demonstrate the analysis of telomerase activity in three regions of the mouse brain by non-denaturing protein extraction using CHAPS lysis buffer followed by modification of the standard TRAP assay.In this 2-step assay, endogenous telomerase elongates a specific telomerase substrate (TS primer) by adding TTAGGG 6 bp repeats (telomerase reaction). The telomerase reaction products are amplified by PCR reaction creating a DNA ladder of 6 bp increments. The analysis of the DNA ladder is made by 4.5% high resolution agarose gel electrophoresis followed by staining with highly sensitive nucleic acid stain.Compared to the traditional TRAP assay that utilize 32P labeled radioactive dCTP's for DNA detection and polyacrylamide gel electrophoresis for resolving the DNA ladder, this protocol offers a non-toxic time saving TRAP assay for evaluating telomerase activity in the mouse brain, demonstrating the ability to detect differences in telomerase activity in the various female and male mouse brain region.
机译:端粒酶是一种核糖核蛋白,负责维持端粒的长度,从而促进基因组完整性,增殖和寿命。此外,端粒酶保护线粒体免受氧化应激并赋予对细胞凋亡的抗性,表明其对于非有丝分裂,高活性细胞(如神经元)的存活可能具有重要意义。我们以前证明了新型端粒酶激活剂能够增加端粒酶活性和在各种小鼠脑区域中的表达并保护运动神经元细胞免受氧化应激的能力。这些结果强化了端粒酶参与保护神经元免受各种损害的观念。为了强调端粒酶在大脑中的作用,我们在这里比较了雄性和雌性小鼠大脑中端粒酶的活性及其对年龄的依赖性。 TRAP测定法是检测各种组织或细胞系中端粒酶活性的标准方法。在这里,我们展示了通过使用CHAPS裂解缓冲液进行非变性蛋白质提取,然后修改标准TRAP测定法对小鼠大脑三个区域的端粒酶活性进行的分析。在此两步测定法中,内源性端粒酶延长了特定的端粒酶底物(TS)引物)加入TTAGGG 6 bp重复序列(端粒酶反应)。通过PCR反应扩增端粒酶反应产物,产生6bp增量的DNA梯。 DNA阶梯的分析是通过4.5%高分辨率琼脂糖凝胶电泳,然后用高度敏感的核酸染色进行的。与传统的TRAP分析相比,传统的TRAP分析利用 32 P标记的放射性dCTP进行DNA检测和聚丙烯酰胺凝胶电泳用于解析DNA梯形图,该协议提供了一种无毒,节省时间的TRAP分析方法,用于评估小鼠大脑中端粒酶的活性,证明了检测各种雌性和雄性小鼠大脑区域端粒酶活性差异的能力。

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