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Comprehensive transcript analysis in small quantities of mRNA by SAGE-lite.

机译:SAGE-lite对少量mRNA进行全面的转录本分析。

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Serial analysis of gene expression (SAGE) is a powerful technique that can be used for global analysis of gene expression. Its chief advantage over other methods is that SAGE does not require prior knowledge of the genes of interest and provides quantitative and qualitative data of potentially every transcribed sequence in a particular tissue or cell type. Furthermore, SAGE can quantify low-abundance transcripts and reliably detect relatively small differences in transcript abundance between cell populations. However, SAGE demands high input levels of mRNA which are often unavailable, particularly when studying human disease. To overcome this limitation, we have developed a modification of SAGE that allows detailed global analysis of gene expression in extremely small quantities of tissue or cultured cells. We have called this approach 'SAGE-Lite'. This technique was used for the global analysis of transcription in samples of normal and pathological human cerebrovasculature to study the molecular pathology of intracranial aneurysms. These samples, which are obtained during operative surgical repair, are typically no bigger than 1 or 2 mm and yield <100 ng of total RNA. In addition, we show that SAGE-Lite allows simple and rapid isolation of long cDNAs from short (15 bp) SAGE sequence tags.
机译:基因表达的序列分析(SAGE)是一项强大的技术,可用于基因表达的全局分析。与其他方法相比,它的主要优势在于SAGE不需要事先了解目标基因,并且可以提供特定组织或细胞类型中每个转录序列的定量和定性数据。此外,SAGE可以量化低丰度的转录本,并可靠地检测细胞群体之间转录本丰度的相对较小的差异。但是,SAGE需要高水平的mRNA输入,而这通常是不可用的,特别是在研究人类疾病时。为克服此限制,我们开发了SAGE的修饰,可以对极少量组织或培养细胞中的基因表达进行详细的全局分析。我们称这种方法为“ SAGE-Lite”。该技术用于正常和病理性人脑血管样品中的转录整体分析,以研究颅内动脉瘤的分子病理学。这些在手术修复过程中获得的样品通常不大于1或2 mm,并且产生的总RNA小于100 ng。此外,我们显示SAGE-Lite允许从短(15 bp)SAGE序列标签简单快速地分离长cDNA。

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