Nielsen Kåre Lehmann
Department of Life Sciences, University of Aalborg, Aalborg, Denmark.
Methods Mol Biol. 2008;387:109-20. doi: 10.1007/978-1-59745-454-4_8.
Serial analysis of gene expression (SAGE) studies often yield numerous tags that cannot be mapped to known gene sequences. Intriguingly, these may represent unknown genes, unknown parts of genes, or transcript variants. In order to elucidate the origin of these tags, 3'- and 5'-rapid amplification of complementary DNA ends (RACE) reactions can be performed using primers identical or complementary to SAGE tags. This way, transcript fragments, or indeed the entire uncharacterized transcript, can be cloned and sequenced.
基因表达序列分析(SAGE)研究常常产生许多无法映射到已知基因序列的标签。有趣的是,这些标签可能代表未知基因、基因的未知部分或转录变体。为了阐明这些标签的来源,可以使用与SAGE标签相同或互补的引物进行3'和5'互补DNA末端快速扩增(RACE)反应。通过这种方式,可以克隆并测序转录片段,甚至是整个未表征的转录本。