Jackson P David, Harrington John J
Athersys Inc., 3201 Carnegie Ave., Cleveland, OH 44115, USA.
Drug Discov Today. 2005 Jan 1;10(1):53-60. doi: 10.1016/S1359-6446(04)03303-3.
High-throughput target discovery requires robust disease models and the ability to rapidly survey the genome for function. In the post-genomics era, there has been a strong emphasis placed upon "gene-to-function" approaches that take advantage of the large amount of gene sequence information now available. Here, we advocate a return to "function-to-gene" approaches as a first step in target discovery (and validation), followed by hypothesis-driven research to validate new targets identified by their activity in cell-based disease models.
高通量靶点发现需要强大的疾病模型以及快速在基因组中探寻功能的能力。在后基因组时代,人们大力强调利用现有的大量基因序列信息的“基因到功能”方法。在此,我们主张回归“功能到基因”方法,将其作为靶点发现(及验证)的第一步,随后开展基于假设的研究,以验证在细胞疾病模型中通过其活性鉴定出的新靶点。