Sardiu Mihaela E, Gilmore Joshua M, Groppe Brad D, Herman Damir, Ramisetty Sreenivasa R, Cai Yong, Jin Jingji, Conaway Ronald C, Conaway Joan W, Florens Laurence, Washburn Michael P
Stowers Institute for Medical Research, Kansas City, MO, USA.
Ayasdi, Inc., Palo Alto, CA, USA.
EMBO Rep. 2015 Jan;16(1):116-26. doi: 10.15252/embr.201439403. Epub 2014 Nov 26.
The study of conserved protein interaction networks seeks to better understand the evolution and regulation of protein interactions. Here, we present a quantitative proteomic analysis of 18 orthologous baits from three distinct chromatin-remodeling complexes in Saccharomyces cerevisiae and Homo sapiens. We demonstrate that abundance levels of orthologous proteins correlate strongly between the two organisms and both networks have highly similar topologies. We therefore used the protein abundances in one species to cross-predict missing protein abundance levels in the other species. Lastly, we identified a novel conserved low-abundance subnetwork further demonstrating the value of quantitative analysis of networks.
对保守蛋白质相互作用网络的研究旨在更好地理解蛋白质相互作用的进化和调控。在此,我们对酿酒酵母和人类中三种不同染色质重塑复合物的18个直系同源诱饵进行了定量蛋白质组学分析。我们证明,两种生物之间直系同源蛋白质的丰度水平密切相关,且两个网络具有高度相似的拓扑结构。因此,我们利用一个物种中的蛋白质丰度来交叉预测另一个物种中缺失的蛋白质丰度水平。最后,我们鉴定出一个新的保守低丰度子网,进一步证明了网络定量分析的价值。