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Novel subtractive transcription-based amplification of mRNA (STAR) method and its application in search of rare and differentially expressed genes in AD brains

机译:基于减法转录的新型mRNA扩增(STAR)方法及其在AD大脑中稀有和差异表达基因的搜索中的应用

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摘要

Background: Alzheimer's disease (AD) is a complex disorder that involves multiple biological processes. Many genes implicated in these processes may be present in low abundance in the human brain. DNA microarray analysis identifies changed genes that are expressed at high or moderate levels. Complementary to this approach, we described here a novel technology designed specifically to isolate rare and novel genes previously undetectable by other methods. We have used this method to identify differentially expressed genes in brains affected by AD. Our method, termed Subtractive Transcription-based Amplification of mRNA (STAR), is a combination of subtractive RNA/DNA hybridization and RNA amplification, which allows the removal of non-differentially expressed transcripts and the linear amplification of the differentially expressed genes. Results: Using the STAR technology we have identified over 800 differentially expressed sequences in AD brains, both up- and down- regulated, compared to age-matched controls. Over 55% of the sequences represent genes of unknown function and roughly half of them were novel and rare discoveries in the human brain. The expression changes of nearly 80 unique genes were further confirmed by qRT-PCR and the association of additional genes with AD and/or neurodegeneration was established using an in-house literature mining tool (LitMiner). Conclusion: The STAR process significantly amplifies unique and rare sequences relative to abundant housekeeping genes and, as a consequence, identifies genes not previously linked to AD. This method also offers new opportunities to study the subtle changes in gene expression that potentially contribute to the development and/or progression of AD.
机译:背景:阿尔茨海默氏病(AD)是一种复杂的疾病,涉及多个生物学过程。与这些过程有关的许多基因在人脑中可能以低丰度存在。 DNA微阵列分析可鉴定以高或中等水平表达的改变的基因。作为这种方法的补充,我们在这里描述了一种新颖的技术,专门设计用于分离以前无法通过其他方法检测到的稀有和新颖基因。我们已经使用这种方法来鉴定受AD影响的大脑中差异表达的基因。我们的方法称为基于减法转录的mRNA扩增(STAR),是减法RNA / DNA杂交和RNA扩增的组合,可去除非差异表达的转录本和差异表达基因的线性扩增。结果:与年龄匹配的对照组相比,使用STAR技术,我们已经在AD大脑中鉴定了800多个差异表达的序列,无论是上调还是下调。超过55%的序列代表功能未知的基因,其中约有一半是人脑中的新奇罕见发现。通过qRT-PCR进一步证实了将近80个独特基因的表达变化,并使用内部文献挖掘工具(LitMiner)建立了其他基因与AD和/或神经变性的关联。结论:相对于丰富的管家基因,STAR过程显着扩增了独特而稀有的序列,因此,鉴定出了以前与AD不相关的基因。该方法还提供了新的机会来研究基因表达的细微变化,这些细微变化可能有助于AD的发展和/或发展。

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