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Differential genetic interactions of yeast stress response MAPK pathways.

dc.contributor.authorMartín, Humberto
dc.contributor.authorShales, Michael
dc.contributor.authorFernandez-Piñar, Pablo
dc.contributor.authorWei, Ping
dc.contributor.authorMolina, María
dc.contributor.authorFiedler, Dorothea
dc.contributor.authorShokat, Kevan M.
dc.contributor.authorBeltrao, Pedro
dc.contributor.authorLim, Wendell
dc.contributor.authorKrogan, Nevan J.
dc.date.accessioned2023-06-18T06:47:44Z
dc.date.available2023-06-18T06:47:44Z
dc.date.issued2015-04-17
dc.description.abstractGenetic interaction screens have been applied with great success in several organisms to study gene function and the genetic architecture of the cell. However, most studies have been performed under optimal growth conditions even though many functional interactions are known to occur under specific cellular conditions. In this study, we have performed a large-scale genetic interaction analysis in Saccharomyces cerevisiae involving approximately 49 × 1,200 double mutants in the presence of five different stress conditions, including osmotic, oxidative and cell wall-altering stresses. This resulted in the generation of a differential E-MAP (or dE-MAP) comprising over 250,000 measurements of conditional interactions. We found an extensive number of conditional genetic interactions that recapitulate known stress-specific functional associations. Furthermore, we have also uncovered previously unrecognized roles involving the phosphatase regulator Bud14, the histone methylation complex COMPASS and membrane trafficking complexes in modulating the cell wall integrity pathway. Finally, the osmotic stress differential genetic interactions showed enrichment for genes coding for proteins with conditional changes in phosphorylation but not for genes with conditional changes in gene expression. This suggests that conditional genetic interactions are a powerful tool to dissect the functional importance of the different response mechanisms of the cell.
dc.description.departmentDepto. de Microbiología y Parasitología
dc.description.facultyFac. de Farmacia
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Ciencia e Innovación (MICINN)
dc.description.sponsorshipMinisterio de Ciencia y Competitividad (MINECO)
dc.description.sponsorshipNIH
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/33654
dc.identifier.doi10.15252/msb.20145606
dc.identifier.issn1744-4292
dc.identifier.officialurlhttp://dx.doi.org/10.15252/msb.20145606
dc.identifier.urihttps://hdl.handle.net/20.500.14352/24209
dc.issue.number4
dc.journal.titleMolecular systems biology
dc.language.isoeng
dc.page.initial800
dc.publisherEMBO Press
dc.relation.projectIDBIO2010-22369-C02-01
dc.relation.projectIDBIO2013-44112-P
dc.relation.projectIDGM084448
dc.relation.projectIDGM084279
dc.relation.projectIDGM098101
dc.relation.projectIDR01 GM107671
dc.rightsAtribución 3.0 España
dc.rights.accessRightsopen access
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/es/
dc.subject.cdu579
dc.subject.keywordcell wall integrity
dc.subject.keywordgenetic interactions
dc.subject.keywordosmotic shock
dc.subject.keywordstress response
dc.subject.keywordChromatin
dc.subject.keywordEpigenetics
dc.subject.keywordGenomics & Functional Genomics
dc.subject.keywordNetwork Biology
dc.subject.ucmMicrobiología (Farmacia)
dc.subject.unesco3302.03 Microbiología Industrial
dc.titleDifferential genetic interactions of yeast stress response MAPK pathways.
dc.typejournal article
dc.volume.number11
dspace.entity.typePublication

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