Epistasis analysis with global transcriptional phenotypes

被引:74
|
作者
Van Driessche, N
Demsar, J
Booth, EO
Hill, P
Juvan, P
Zupan, B
Kuspa, A
Shaulsky, G
机构
[1] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[2] Baylor Coll Med, Grad Program Dev Biol, Houston, TX 77030 USA
[3] Univ Ljubljana, Fac Comp & Informat Sci, Ljubljana, Slovenia
[4] Baylor Coll Med, Verna & Marrs McLean Dept Biochem & Mol Biol, Houston, TX 77030 USA
[5] Baylor Coll Med, Grad Program Struct Computat Biol & Mol Biophys, Houston, TX 77030 USA
关键词
D O I
10.1038/ng1545
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Classical epistasis analysis can determine the order of function of genes in pathways using morphological, biochemical and other phenotypes. It requires knowledge of the pathway's phenotypic output and a variety of experimental expertise and so is unsuitable for genome-scale analysis. Here we used microarray profiles of mutants as phenotypes for epistasis analysis. Considering genes that regulate activity of protein kinase A in Dictyostelium, we identified known and unknown epistatic relationships and reconstructed a genetic network with microarray phenotypes alone. This work shows that microarray data can provide a uniform, quantitative tool for large-scale genetic network analysis.
引用
收藏
页码:471 / 477
页数:7
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