Boston University, Boston, MA 02215, USA.
Adv Exp Med Biol. 2012;751:53-78. doi: 10.1007/978-1-4614-3567-9_3.
Understanding how genetic modifications, individual or in combinations, affect phenotypes is a challenge common to several areas of biology, including human genetics, metabolic engineering, and evolutionary biology. Much of the complexity of how genetic modifications produce phenotypic outcomes has to do with the lack of independence, or epistasis, between different perturbations: the phenotypic effect of one perturbation depends, in general, on the genetic background of previously accumulated modifications, i.e., on the network of interactions with other perturbations. In recent years, an increasing number of high-throughput efforts, both experimental and computational, have focused on trying to unravel these genetic interaction networks. Here we provide an overview of how systems biology approaches have contributed to, and benefited from, the study of genetic interaction networks. We focus, in particular, on results pertaining to the global multilevel properties of these networks, and the connection between their modular architecture and their functional and evolutionary significance.
理解遗传修饰(个体或组合)如何影响表型是生物学多个领域(包括人类遗传学、代谢工程和进化生物学)共同面临的挑战。遗传修饰如何产生表型结果的复杂性在很大程度上与不同扰动之间缺乏独立性(或上位性)有关:一个扰动的表型效应通常取决于先前积累的修饰的遗传背景,即与其他扰动的相互作用网络。近年来,越来越多的高通量实验和计算努力都集中在试图解开这些遗传相互作用网络上。本文概述了系统生物学方法如何为遗传相互作用网络的研究做出贡献并从中受益。我们特别关注与这些网络的全局多层次特性以及它们的模块化结构与其功能和进化意义之间的联系有关的结果。