Manev Hari, Manev Radmila
Department of Psychiatry, University of Illinois at Chicago, Chicago, IL 60612, USA.
Cardiovasc Psychiatry Neurol. 2010;2010:838164. doi: 10.1155/2010/838164. Epub 2010 Jun 27.
Phenomics is a systematic study of phenotypes on a genomewide scale that is expected to unravel, as of yet, unsuspected functional roles of the genome. It remains to be determined how to optimally approach and analyze the available phenomics databases to spearhead innovation in neuropsychiatry. By serendipitously connecting two unrelated phenotypes of increased blood levels of the adipokine leptin, a molecule that regulates appetite, in 5-lipoxygenase- (5-LOX) deficient mice and patients with a lower risk for Alzheimer's disease (AD), we postulated a leptin-mediated basis for beneficial effects of ALOX5 (a gene encoding 5-LOX) gene-deficiency in AD. We suggest that it might be possible to avoid relying on serendipity and develop data-mining tools capable of extracting from phenomics databases indications for such novel hypotheses. Hence, we provide an example of using a free-access Arrowsmith two-node search interface to identify ALOX5 as unsuspected putative mechanisms for the previously described clinical association between increased plasma levels of leptin and a lower risk of incident dementia and AD.
表型组学是在全基因组范围内对表型进行的系统研究,有望揭示基因组尚未被怀疑的功能作用。如何以最佳方式处理和分析现有的表型组学数据库以引领神经精神病学的创新仍有待确定。通过意外地将两种不相关的表型联系起来,即脂肪因子瘦素(一种调节食欲的分子)血液水平升高在5-脂氧合酶(5-LOX)缺陷小鼠和患阿尔茨海默病(AD)风险较低的患者中的表现,我们推测了ALOX5(一种编码5-LOX的基因)基因缺陷在AD中产生有益作用的瘦素介导基础。我们认为有可能避免依赖偶然性,开发能够从表型组学数据库中提取此类新假设线索的数据挖掘工具。因此,我们提供了一个使用免费访问的Arrowsmith双节点搜索界面的例子,以确定ALOX5是先前描述的瘦素血浆水平升高与痴呆症和AD发病风险降低之间临床关联的未被怀疑的潜在机制。