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MicroSAGE: a modified procedure for serial analysis of gene expression in limited amounts of tissue.

机译:MicroSAGE:一种改进的方法,用于在有限量的组织中进行基因表达的系列分析。

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Serial Analysis of Gene Expression (SAGE) is a powerful expression profiling method, allowing the analysis of the expression of thousands of transcripts simultaneously. A disadvantage of the method, however, is the relatively high amount of input RNA required. Consequently, SAGE cannot be used for the generation of expression profiles when RNA is limited, i.e. in small biological samples such as tissue biopsies or microdissected material. Here we describe a modification of SAGE, named microSAGE, which requires 500- to 5000-fold less starting material. Compared with SAGE, microSAGE is simplified due to incorporation of a 'single-tube' procedure for all steps from RNA isolation to tag release. Furthermore, a limited number of additional PCR cycles are performed. Using microSAGE gene expression profiles can be obtained from minute quantities of tissue such as a single hippocampal punch from a rat brain slice of 325 micrometers thickness, estimated to contain, at most, 10(5) cells. This method opens up a multitude of new possibilities for the application of SAGE, for example the characterization of expression profiles in tissue biopsies, tumor metastases or in other cases where tissue is scarce and the generation of region-specific expression profiles of complex heterogeneous tissues.
机译:基因表达的序列分析(SAGE)是一种功能强大的表达谱分析方法,可以同时分析成千上万个转录本的表达。然而,该方法的缺点是需要相对大量的输入RNA。因此,当RNA受到限制时,即在小的生物样品如组织活检或显微解剖的材料中,SAGE不能用于表达谱的产生。在这里,我们描述了一种名为SAGE的SAGE变体,它需要少500到5000倍的起始原料。与SAGE相比,由于从RNA分离到标签释放的所有步骤都采用了“单管”程序,因此microSAGE得以简化。此外,执行了有限数量的其他PCR循环。使用microSAGE基因表达谱可以从微量组织获得,例如从325微米厚的大鼠脑片(估计最多包含10(5)个细胞)的单个海马穿孔器获得。这种方法为SAGE的应用开辟了许多新的可能性,例如在组织活检,肿瘤转移或组织稀缺的其他情况下表达谱的表征,以及复杂异质组织的区域特异性表达谱的生成。

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