Defining genetic interaction

被引:318
作者
Mani, Ramamurthy [1 ]
Onge, Robert P. St. [2 ]
Hartman, John L. [3 ]
Giaever, Guri [4 ]
Roth, Frederick P. [1 ,5 ]
机构
[1] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[2] Stanford Univ, Dept Biochem, Stanford, CA 94305 USA
[3] Univ Alabama, Dept Genet, Birmingham, AL 35294 USA
[4] Univ Toronto, Leslie Dan Fac Pharm, Donnelly Ctr Cellular & Biomol Res, Dept Pharmaceut Sci, Toronto, ON M5S 3E1, Canada
[5] Dana Farber Canc Inst, Ctr Canc Syst Biol, Boston, MA 02115 USA
关键词
epistasis; fitness; gene function;
D O I
10.1073/pnas.0712255105
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
Sometimes mutations in two genes produce a phenotype that is surprising in light of each mutation's individual effects. This phenomenon, which defines genetic interaction, can reveal functional relationships between genes and pathways. For example, double mutants with surprisingly slow growth define synergistic interactions that can identify compensatory pathways or protein complexes. Recent studies have used four mathematically distinct definitions of genetic interaction (here termed Product, Additive, Log, and Min). Whether this choice holds practical consequences has not been clear, because the definitions yield identical results under some conditions. Here, we show that the choice among alternative definitions can have profound consequences. Although 52% of known synergistic genetic interactions in Saccharomyces cerevisiae were inferred according to the Min definition, we find that both Product and Log definitions (shown here to be practically equivalent) are better than Min for identifying functional relationships. Additionally, we show that the Additive and Log definitions, each commonly used in population genetics, lead to differing conclusions related to the selective advantages of sexual reproduction.
引用
收藏
页码:3461 / 3466
页数:6
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