Soares Marcelo Bento, de Fatima Bonaldo Maria, Hackett Jeremiah D, Bhattacharya Debashish
Children's Memorial Research Center, Northwestern University's Feinberg School of Medicine, Chicago, IL, USA.
Methods Mol Biol. 2009;533:109-22. doi: 10.1007/978-1-60327-136-3_6.
Expressed Sequence Tags (ESTs) provide a rapid and efficient approach for gene discovery and analysis of gene expression in eukaryotes. ESTs have also become particularly important with recent expanded efforts in complete genome sequencing of understudied, nonmodel eukaryotes such as protists and algae. For these projects, ESTs provide an invaluable source of data for gene identification and prediction of exon-intron boundaries. The generation of EST data, although straightforward in concept, requires nonetheless great care to ensure the highest efficiency and return for the investment in time and funds. To this end, key steps in the process include generation of a normalized cDNA library to facilitate a high gene discovery rate followed by serial subtraction of normalized libraries to maintain the discovery rate. Here we describe in detail, protocols for normalization and subtraction of cDNA libraries followed by an example using the toxic dinoflagellate Alexandrium tamarense.
表达序列标签(ESTs)为真核生物中的基因发现和基因表达分析提供了一种快速有效的方法。随着最近对诸如原生生物和藻类等研究较少的非模式真核生物进行全基因组测序的努力不断扩大,ESTs也变得尤为重要。对于这些项目,ESTs为基因识别和外显子-内含子边界预测提供了宝贵的数据来源。EST数据的生成,尽管在概念上很简单,但仍需要格外小心,以确保在时间和资金投入上获得最高效率和回报。为此,该过程中的关键步骤包括生成标准化的cDNA文库以促进高基因发现率,随后对标准化文库进行连续扣除以维持发现率。在这里,我们详细描述了cDNA文库标准化和扣除的方案,并以有毒甲藻塔玛亚历山大藻为例进行说明。