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dc.contributor.authorPeñalva, Miguel Ángel-
dc.contributor.authorTilburn, Joan-
dc.contributor.authorBignell, Elaine-
dc.contributor.authorArst, Herbert Nathan Jr.-
dc.date.accessioned2012-10-05T12:41:06Z-
dc.date.available2012-10-05T12:41:06Z-
dc.date.issued2008-06-
dc.identifier.citationTrends in Microbiology 16(6):291-300(2008)es_ES
dc.identifier.issn0966-842X-
dc.identifier.urihttp://hdl.handle.net/10261/57402-
dc.description10 páginas, 3 figuras, I figura, 1 tabla -- PAGS nros. 291-300es_ES
dc.description.abstractMany fungi grow over a wide pH range and their gene expression is tailored to the environmental pH. In Aspergillus nidulans, the transcription factor PacC, an activator of genes expressed in alkaline conditions and a repressor of those expressed in acidic conditions, undergoes two processing proteolyses, the first being pH-signal dependent and the second proteasomal. Signal transduction involves a 'go-between' connecting two complexes, one of which comprises two plasma membrane proteins and an arrestin and the other comprises PacC, a cysteine protease, a scaffold and endosomal components. The Saccharomyces cerevisiae PacC orthologue, Rim101p, differs in that it does not undergo the second round of proteolysis and it functions directly as a repressor only. PacC/Rim101-mediated pH regulation is crucial to fungal pathogenicityes_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsclosedAccesses_ES
dc.titleAmbient pH gene regulation in fungi: making connectionses_ES
dc.typeartículoes_ES
dc.identifier.doi10.1016/j.tim.2008.03.006-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttp://dx.doi.org/10.1016/j.tim.2008.03.006es_ES
dc.identifier.e-issn1878-4380-
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.fulltextNo Fulltext-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeartículo-
item.cerifentitytypePublications-
item.grantfulltextnone-
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