TY - JOUR
T1 - Functional overlap and regulatory links shape genetic interactions between signaling pathways
AU - Van Wageningen, Sake
AU - Kemmeren, Patrick
AU - Lijnzaad, Philip
AU - Margaritis, Thanasis
AU - Benschop, Joris J.
AU - De Castro, Inês J.
AU - Van Leenen, Dik
AU - Groot Koerkamp, Marian J.A.
AU - Ko, Cheuk W.
AU - Miles, Antony J.
AU - Brabers, Nathalie
AU - Brok, Mariel O.
AU - Lenstra, Tineke L.
AU - Fiedler, Dorothea
AU - Fokkens, Like
AU - Aldecoa, Rodrigo
AU - Apweiler, Eva
AU - Taliadouros, Virginia
AU - Sameith, Katrin
AU - Van De Pasch, Loes A.L.
AU - Van Hooff, Sander R.
AU - Bakker, Linda V.
AU - Krogan, Nevan J.
AU - Snel, Berend
AU - Holstege, Frank C.P.
N1 - Funding Information:
This work was supported by the Netherlands Bioinformatics Centre (NBIC) and the Netherlands Organization of Scientific Research (NWO), grants 016.108.607, 817.02.015, 050.71.057, 911.06.009, 021.002.035 (T.L.L.), 863.07.007 (P.K.), 700.57.407 (J.J.B.).
PY - 2010/12/10
Y1 - 2010/12/10
N2 - To understand relationships between phosphorylation-based signaling pathways, we analyzed 150 deletion mutants of protein kinases and phosphatases in S. cerevisiae using DNA microarrays. Downstream changes in gene expression were treated as a phenotypic readout. Double mutants with synthetic genetic interactions were included to investigate genetic buffering relationships such as redundancy. Three types of genetic buffering relationships are identified: mixed epistasis, complete redundancy, and quantitative redundancy. In mixed epistasis, the most common buffering relationship, different gene sets respond in different epistatic ways. Mixed epistasis arises from pairs of regulators that have only partial overlap in function and that are coupled by additional regulatory links such as repression of one by the other. Such regulatory modules confer the ability to control different combinations of processes depending on condition or context. These properties likely contribute to the evolutionary maintenance of paralogs and indicate a way in which signaling pathways connect for multiprocess control.
AB - To understand relationships between phosphorylation-based signaling pathways, we analyzed 150 deletion mutants of protein kinases and phosphatases in S. cerevisiae using DNA microarrays. Downstream changes in gene expression were treated as a phenotypic readout. Double mutants with synthetic genetic interactions were included to investigate genetic buffering relationships such as redundancy. Three types of genetic buffering relationships are identified: mixed epistasis, complete redundancy, and quantitative redundancy. In mixed epistasis, the most common buffering relationship, different gene sets respond in different epistatic ways. Mixed epistasis arises from pairs of regulators that have only partial overlap in function and that are coupled by additional regulatory links such as repression of one by the other. Such regulatory modules confer the ability to control different combinations of processes depending on condition or context. These properties likely contribute to the evolutionary maintenance of paralogs and indicate a way in which signaling pathways connect for multiprocess control.
KW - CELLBIO
KW - SIGNALING
UR - http://www.scopus.com/inward/record.url?scp=78649938122&partnerID=8YFLogxK
U2 - 10.1016/j.cell.2010.11.021
DO - 10.1016/j.cell.2010.11.021
M3 - Article
C2 - 21145464
AN - SCOPUS:78649938122
SN - 0092-8674
VL - 143
SP - 991
EP - 1004
JO - Cell
JF - Cell
IS - 6
ER -