Reconstructing the temporal progression of HIV-1 immune response pathways

被引:9
|
作者
Jain, Siddhartha [1 ]
Arrais, Joel [2 ]
Venkatachari, Narasimhan J. [3 ]
Ayyavoo, Velpandi [3 ]
Bar-Joseph, Ziv [4 ]
机构
[1] Carnegie Mellon Univ, Dept Comp Sci, Pittsburgh, PA 15213 USA
[2] Univ Coimbra, Dept Comp Sci, Coimbra, Portugal
[3] Univ Pittsburgh, Dept Infect Dis, Pittsburgh, PA USA
[4] Carnegie Mellon Univ, Computat Biol & Machine Learning Dept, Pittsburgh, PA 15213 USA
基金
美国国家科学基金会;
关键词
IMMUNODEFICIENCY-VIRUS TYPE-1; NF-KAPPA-B; DYNAMIC REGULATORY NETWORKS; MICRORNA REGULATION; EXPRESSION ANALYSIS; HLA-C; RNA; TRANSCRIPTION; KINASE; REPLICATION;
D O I
10.1093/bioinformatics/btw254
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Most methods for reconstructing response networks from high throughput data generate static models which cannot distinguish between early and late response stages. Results: We present TimePath, a new method that integrates time series and static datasets to reconstruct dynamic models of host response to stimulus. TimePath uses an Integer Programming formulation to select a subset of pathways that, together, explain the observed dynamic responses. Applying TimePath to study human response to HIV-1 led to accurate reconstruction of several known regulatory and signaling pathways and to novel mechanistic insights. We experimentally validated several of TimePaths' predictions highlighting the usefulness of temporal models.
引用
收藏
页码:253 / 261
页数:9
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