Harnessing gene expression to identify the genetic basis of drug resistance

被引:36
作者
Chen, Bo-Juen [2 ,3 ]
Causton, Helen C.
Mancenido, Denesy
Goddard, Noel L. [4 ]
Perlstein, Ethan O. [5 ]
Pe'er, Dana [1 ,3 ]
机构
[1] Columbia Univ, Dept Biol Sci, Fairchild Ctr 607D, New York, NY 10027 USA
[2] Columbia Univ, Dept Biomed Informat, New York, NY 10027 USA
[3] Columbia Univ, Ctr Computat Biol & Bioinformat, New York, NY 10027 USA
[4] CUNY Hunter Coll, Dept Phys & Astron, New York, NY 10021 USA
[5] Princeton Univ, Lewis Sigler Inst Integrat Genom, Princeton, NJ 08544 USA
基金
美国国家卫生研究院;
关键词
complex trait analysis; drug target/off-target discovery; genetical genomics; PROTEIN-KINASE-A; RNA-BINDING PROTEIN; SACCHAROMYCES-CEREVISIAE; CELL-DEATH; MITOCHONDRIAL BIOGENESIS; TRANSCRIPTION ACTIVATOR; MESSENGER-RNA; BUDDING YEAST; CYCLIC-AMP; DISEASE;
D O I
10.1038/msb.2009.69
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The advent of cost-effective genotyping and sequencing methods have recently made it possible to ask questions that address the genetic basis of phenotypic diversity and how natural variants interact with the environment. We developed Camelot (CAusal Modelling with Expression Linkage for cOmplex Traits), a statistical method that integrates genotype, gene expression and phenotype data to automatically build models that both predict complex quantitative phenotypes and identify genes that actively influence these traits. Camelot integrates genotype and gene expression data, both generated under a reference condition, to predict the response to entirely different conditions. We systematically applied our algorithm to data generated from a collection of yeast segregants, using genotype and gene expression data generated under drug-free conditions to predict the response to 94 drugs and experimentally confirmed 14 novel gene-drug interactions. Our approach is robust, applicable to other phenotypes and species, and has potential for applications in personalized medicine, for example, in predicting how an individual will respond to a previously unseen drug. Molecular Systems Biology 5: 310; published online 13 October 2009; doi:10.1038/msb.2009.69
引用
收藏
页数:14
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