Integrative Modeling Defines the Nova Splicing-Regulatory Network and Its Combinatorial Controls

被引:226
作者
Zhang, Chaolin [1 ]
Frias, Maria A. [1 ]
Mele, Aldo [1 ]
Ruggiu, Matteo [1 ]
Eom, Taesun [1 ]
Marney, Christina B. [1 ]
Wang, Huidong [1 ]
Licatalosi, Donny D. [1 ]
Fak, John J. [1 ]
Darnell, Robert B. [1 ]
机构
[1] Rockefeller Univ, Howard Hughes Med Inst, Mol Neurooncol Lab, New York, NY 10021 USA
关键词
PROTEIN INTERACTIONS; INSIGHTS; INCLUSION; SWITCH; MOTIF;
D O I
10.1126/science.1191150
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The control of RNA alternative splicing is critical for generating biological diversity. Despite emerging genome-wide technologies to study RNA complexity, reliable and comprehensive RNA-regulatory networks have not been defined. Here, we used Bayesian networks to probabilistically model diverse data sets and predict the target networks of specific regulators. We applied this strategy to identify similar to 700 alternative splicing events directly regulated by the neuron-specific factor Nova in the mouse brain, integrating RNA-binding data, splicing microarray data, Nova-binding motifs, and evolutionary signatures. The resulting integrative network revealed combinatorial regulation by Nova and the neuronal splicing factor Fox, interplay between phosphorylation and splicing, and potential links to neurologic disease. Thus, we have developed a general approach to understanding mammalian RNA regulation at the systems level.
引用
收藏
页码:439 / 443
页数:5
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