Title of article
Functional Organization of the S. cerevisiae Phosphorylation Network
Author/Authors
Dorothea Fiedler، نويسنده , , Hannes Braberg، نويسنده , , Monika Mehta، نويسنده , , Gal Chechik، نويسنده , , Gerard Cagney، نويسنده , , Paromita Mukherjee، نويسنده , , Andrea C. Silva، نويسنده , , Michael Shales، نويسنده , , Sean R. Collins، نويسنده , , Sake van Wageningen، نويسنده , , Patrick Kemmeren، نويسنده , , Frank C.P. Holstege، نويسنده , , Jonathan S. Weissman، نويسنده , , Michael-Christopher Keogh، نويسنده , , Daphne Koller، نويسنده , , Kevan M. Shokat، نويسنده , , Nevan J. Krogan، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2009
Pages
12
From page
952
To page
963
Abstract
Reversible protein phosphorylation is a signaling mechanism involved in all cellular processes. To create a systems view of the signaling apparatus in budding yeast, we generated an epistatic miniarray profile (E-MAP) comprised of 100,000 pairwise, quantitative genetic interactions, including virtually all protein and small-molecule kinases and phosphatases as well as key cellular regulators. Quantitative genetic interaction mapping reveals factors working in compensatory pathways (negative genetic interactions) or those operating in linear pathways (positive genetic interactions). We found an enrichment of positive genetic interactions between kinases, phosphatases, and their substrates. In addition, we assembled a higher-order map from sets of three genes that display strong interactions with one another: triplets enriched for functional connectivity. The resulting network view provides insights into signaling pathway regulation and reveals a link between the cell-cycle kinase, Cak1, the Fus3 MAP kinase, and a pathway that regulates chromatin integrity during transcription by RNA polymerase II.
Journal title
CELL
Serial Year
2009
Journal title
CELL
Record number
1019659
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