利用功能连锁基因网络研究人类疾病

B. Linghu, Guohui Liu, Yu Xia
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引用次数: 1

摘要

后基因组时代的一个主要挑战是了解单个基因的特定细胞功能以及这些基因的功能障碍如何导致不同的疾病。作为系统生物学的一个新兴领域,基因网络已经被用来揭示基因功能和人类疾病。在本章中,首先证明了在共同的生物学过程中工作的基因或与共同疾病有关的基因的功能关联的存在。其次,综述了基于基因组学和蛋白质组学数据整合构建功能连锁基因网络(FLN)的方法。最后,综述了基于fln的两种疾病相关应用:预测新的疾病基因和治疗靶点,以及在分子水平上识别疾病-疾病关联。这两种应用都为疾病的分子机制带来了新的见解,并为药物发现提供了新的机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Using Functional Linkage Gene Networks to Study Human Diseases
A major challenge in the post-genomic era is to understand the specific cellular functions of individual genes and how dysfunctions of these genes lead to different diseases. As an emerging area of systems biology, gene networks have been used to shed light on gene function and human disease. In this chapter, first the existence of functional association for genes working in a common biological process or implicated in a common disease is demonstrated. Next, approaches to construct the functional linkage gene network (FLN) based on genomic and proteomic data integration are reviewed. Finally, two FLNbased applications related to diseases are reviewed: prediction of new disease genes and therapeutic targets, and identification of disease-disease associations at the molecular level. Both of these applications bring new insights into the molecular mechanisms of diseases, and provide new opportunities for drug discovery.
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