Reverse engineering gene networks:: Integrating genetic perturbations with dynamical modeling

被引:289
作者
Tegnér, J [1 ]
Yeung, MKS
Hasty, J
Collins, JJ
机构
[1] Boston Univ, Ctr BioDynam, Boston, MA 02215 USA
[2] Boston Univ, Dept Biomed Engn, Boston, MA 02215 USA
[3] Linkoping Univ, Div Computat Biol, Dept Phys, S-58183 Linkoping, Sweden
[4] Stockholm Bioinformat Ctr, Stockholm Ctr Phys Astron & Biotechnol, S-10691 Stockholm, Sweden
[5] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
关键词
D O I
10.1073/pnas.0933416100
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
While the fundamental building blocks of biology are being tabulated by the various genome projects, microarray technology is setting the stage for the task of deducing the connectivity of large-scale gene networks. We show how the perturbation of carefully chosen genes in a microarray experiment can be used in conjunction with a reverse engineering algorithm to reveal the architecture of an underlying gene regulatory network. Our iterative scheme identifies the network topology by analyzing the steady-state changes in gene expression resulting from the systematic perturbation of a particular node in the network. We highlight the validity of our reverse engineering approach through the successful deduction of the topology of a linear in numero gene network and a recently reported model for the segmentation polarity network in Drosophila melanogaster. Our method may prove useful in identifying and validating specific drug targets and in deconvolving the effects of chemical compounds.
引用
收藏
页码:5944 / 5949
页数:6
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