Tegge Allison N, Sharp Nicholas, Murali T M
Department of Computer Science, Department of Statistics and.
Department of Computer Science.
Bioinformatics. 2016 Jan 15;32(2):242-51. doi: 10.1093/bioinformatics/btv549. Epub 2015 Sep 23.
Cells communicate with their environment via signal transduction pathways. On occasion, the activation of one pathway can produce an effect downstream of another pathway, a phenomenon known as crosstalk. Existing computational methods to discover such pathway pairs rely on simple overlap statistics.
We present Xtalk, a path-based approach for identifying pairs of pathways that may crosstalk. Xtalk computes the statistical significance of the average length of multiple short paths that connect receptors in one pathway to the transcription factors in another. By design, Xtalk reports the precise interactions and mechanisms that support the identified crosstalk. We applied Xtalk to signaling pathways in the KEGG and NCI-PID databases. We manually curated a gold standard set of 132 crosstalking pathway pairs and a set of 140 pairs that did not crosstalk, for which Xtalk achieved an area under the receiver operator characteristic curve of 0.65, a 12% improvement over the closest competing approach. The area under the receiver operator characteristic curve varied with the pathway, suggesting that crosstalk should be evaluated on a pathway-by-pathway level. We also analyzed an extended set of 658 pathway pairs in KEGG and to a set of more than 7000 pathway pairs in NCI-PID. For the top-ranking pairs, we found substantial support in the literature (81% for KEGG and 78% for NCI-PID). We provide examples of networks computed by Xtalk that accurately recovered known mechanisms of crosstalk.
The XTALK software is available at http://bioinformatics.cs.vt.edu/~murali/software. Crosstalk networks are available at http://graphspace.org/graphs?tags=2015-bioinformatics-xtalk.
ategge@vt.edu, murali@cs.vt.edu
Supplementary data are available at Bioinformatics online.
细胞通过信号转导通路与其环境进行通信。有时,一条通路的激活会在另一条通路的下游产生效应,这种现象称为串扰。现有的发现此类通路对的计算方法依赖于简单的重叠统计。
我们提出了Xtalk,一种基于路径的方法来识别可能发生串扰的通路对。Xtalk计算连接一条通路中的受体与另一条通路中的转录因子的多条短路径的平均长度的统计显著性。通过设计,Xtalk报告支持所识别串扰的精确相互作用和机制。我们将Xtalk应用于KEGG和NCI-PID数据库中的信号通路。我们手动策划了一组132个串扰通路对的黄金标准集和一组140个不发生串扰的通路对,Xtalk在接收者操作特征曲线下的面积达到了0.65,比最接近的竞争方法提高了12%。接收者操作特征曲线下的面积因通路而异,这表明串扰应在逐个通路的层面上进行评估。我们还分析了KEGG中658个通路对的扩展集以及NCI-PID中7000多个通路对的集合。对于排名靠前的通路对,我们在文献中找到了大量支持(KEGG为81%,NCI-PID为78%)。我们提供了通过Xtalk计算的网络示例,这些网络准确地恢复了已知的串扰机制。
ategge@vt.edu,murali@cs.vt.edu
补充数据可在《生物信息学》在线获取。