Kramer Michael H, Farré Jean-Claude, Mitra Koyel, Yu Michael Ku, Ono Keiichiro, Demchak Barry, Licon Katherine, Flagg Mitchell, Balakrishnan Rama, Cherry J Michael, Subramani Suresh, Ideker Trey
Department of Medicine, University of California, San Diego, La Jolla, CA 92093, USA.
Section of Molecular Biology, Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093, USA.
Mol Cell. 2017 Feb 16;65(4):761-774.e5. doi: 10.1016/j.molcel.2016.12.024. Epub 2017 Jan 26.
We have developed a general progressive procedure, Active Interaction Mapping, to guide assembly of the hierarchy of functions encoding any biological system. Using this process, we assemble an ontology of functions comprising autophagy, a central recycling process implicated in numerous diseases. A first-generation model, built from existing gene networks in Saccharomyces, captures most known autophagy components in broad relation to vesicle transport, cell cycle, and stress response. Systematic analysis identifies synthetic-lethal interactions as most informative for further experiments; consequently, we saturate the model with 156,364 such measurements across autophagy-activating conditions. These targeted interactions provide more information about autophagy than all previous datasets, producing a second-generation ontology of 220 functions. Approximately half are previously unknown; we confirm roles for Gyp1 at the phagophore-assembly site, Atg24 in cargo engulfment, Atg26 in cytoplasm-to-vacuole targeting, and Ssd1, Did4, and others in selective and non-selective autophagy. The procedure and autophagy hierarchy are at http://atgo.ucsd.edu/.
我们开发了一种通用的渐进式程序——主动相互作用图谱,以指导对编码任何生物系统的功能层次结构进行组装。利用这一过程,我们构建了一个包含自噬的功能本体,自噬是一个与多种疾病相关的核心循环过程。基于酿酒酵母中现有的基因网络构建的第一代模型,捕捉了与囊泡运输、细胞周期和应激反应广泛相关的大多数已知自噬成分。系统分析表明,合成致死相互作用对进一步实验最具信息价值;因此,我们在自噬激活条件下通过156364次此类测量使模型饱和。这些靶向相互作用提供了比以往所有数据集更多的关于自噬的信息,产生了一个包含220个功能的第二代本体。大约一半是以前未知的;我们证实了Gyp1在吞噬泡组装位点、Atg24在货物吞噬、Atg26在细胞质到液泡靶向以及Ssd1、Did4等在选择性和非选择性自噬中的作用。该程序和自噬层次结构可在http://atgo.ucsd.edu/上获取。