Global Mapping of the Yeast Genetic Interaction Network

Amy H.Y. Tong(Memorial Sloan Kettering Cancer Center), Guillaume Lesage(Memorial Sloan Kettering Cancer Center), Gary D. Bader(Memorial Sloan Kettering Cancer Center), Huiming Ding(Memorial Sloan Kettering Cancer Center), Hong Xu(Memorial Sloan Kettering Cancer Center), Xiaofeng Xin(Memorial Sloan Kettering Cancer Center), James D. Young(Memorial Sloan Kettering Cancer Center), Gabriel F. Berriz(Memorial Sloan Kettering Cancer Center), Renée L. Brost(Memorial Sloan Kettering Cancer Center), Michael Chang(Memorial Sloan Kettering Cancer Center), YiQun Chen(Memorial Sloan Kettering Cancer Center), Xin Cheng(Memorial Sloan Kettering Cancer Center), Gordon Chua(Memorial Sloan Kettering Cancer Center), Helena Friesen(Memorial Sloan Kettering Cancer Center), Debra S. Goldberg(Memorial Sloan Kettering Cancer Center), Jennifer Haynes(Memorial Sloan Kettering Cancer Center), Christine Humphries(Memorial Sloan Kettering Cancer Center), Grace He(Memorial Sloan Kettering Cancer Center), Shamiza Hussein(Memorial Sloan Kettering Cancer Center), Lizhu Ke(Memorial Sloan Kettering Cancer Center), Nevan J. Krogan(Memorial Sloan Kettering Cancer Center), Zhijian Li(Memorial Sloan Kettering Cancer Center), Joshua N. Levinson(Memorial Sloan Kettering Cancer Center), Hong Lü(Memorial Sloan Kettering Cancer Center), P Ménard(Memorial Sloan Kettering Cancer Center), Christella Munyana(Memorial Sloan Kettering Cancer Center), Ainslie B. Parsons(Memorial Sloan Kettering Cancer Center), Owen Ryan(Memorial Sloan Kettering Cancer Center), Raffi Tonikian(Memorial Sloan Kettering Cancer Center), Tania Michelle Roberts(Memorial Sloan Kettering Cancer Center), Anne‐Marie Sdicu(Memorial Sloan Kettering Cancer Center), B. Jesse Shapiro(Memorial Sloan Kettering Cancer Center), Bilal Sheikh(Memorial Sloan Kettering Cancer Center), Bernhard Suter(Memorial Sloan Kettering Cancer Center), Sharyl L. Wong(Memorial Sloan Kettering Cancer Center), Lan V. Zhang(Memorial Sloan Kettering Cancer Center), Hongwei Zhu(Memorial Sloan Kettering Cancer Center), Christopher G. Burd(Memorial Sloan Kettering Cancer Center), Sean Munro(Memorial Sloan Kettering Cancer Center), Chris Sander(Memorial Sloan Kettering Cancer Center), Jasper Rine(Memorial Sloan Kettering Cancer Center), Jack Greenblatt(Memorial Sloan Kettering Cancer Center), Matthias Peter(Memorial Sloan Kettering Cancer Center), Anthony Bretscher(Memorial Sloan Kettering Cancer Center), Graham Bell(Memorial Sloan Kettering Cancer Center), Frederick P. Roth(Memorial Sloan Kettering Cancer Center), Grant W. Brown(Memorial Sloan Kettering Cancer Center), Brenda Andrews(Memorial Sloan Kettering Cancer Center), Howard Bussey(Memorial Sloan Kettering Cancer Center), Charles Boone(Memorial Sloan Kettering Cancer Center)
Science
February 5, 2004
Cited by 2,129

Abstract

A genetic interaction network containing approximately 1000 genes and approximately 4000 interactions was mapped by crossing mutations in 132 different query genes into a set of approximately 4700 viable gene yeast deletion mutants and scoring the double mutant progeny for fitness defects. Network connectivity was predictive of function because interactions often occurred among functionally related genes, and similar patterns of interactions tended to identify components of the same pathway. The genetic network exhibited dense local neighborhoods; therefore, the position of a gene on a partially mapped network is predictive of other genetic interactions. Because digenic interactions are common in yeast, similar networks may underlie the complex genetics associated with inherited phenotypes in other organisms.


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