dc.creatorVIEIRA, Andre L. G.
dc.creatorLINARES, Edlaine
dc.creatorAUGUSTO, Ohara
dc.creatorGOMES, Suely L.
dc.date.accessioned2012-10-20T05:20:07Z
dc.date.accessioned2018-07-04T15:47:38Z
dc.date.available2012-10-20T05:20:07Z
dc.date.available2018-07-04T15:47:38Z
dc.date.created2012-10-20T05:20:07Z
dc.date.issued2009
dc.identifierFUNGAL GENETICS AND BIOLOGY, v.46, n.8, p.575-584, 2009
dc.identifier1087-1845
dc.identifierhttp://producao.usp.br/handle/BDPI/30823
dc.identifier10.1016/j.fgb.2009.04.002
dc.identifierhttp://dx.doi.org/10.1016/j.fgb.2009.04.002
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1627462
dc.description.abstractThe sporulation stage of the aquatic fungus Blastocladiella emersonii culminates with the formation and release to the medium of a number of zoospores, which are motile cells responsible for the dispersal of the fungus. The presence in the sporulation solution of 1H-[1,2,4]Oxadiazolo[4,3-a]quinoxalin-1-one (ODQ), a potent and selective inhibitor of nitric oxide-sensitive guanylyl cyclases, completely prevented biogenesis of the zoospores. In addition, this compound was able to significantly reduce cGMP levels, which increase drastically during late sporulation, suggesting the existence of a nitric oxide-dependent mechanism for cGMP synthesis. Furthermore, increased levels of nitric oxide-derived products were detected during sporulation by fluorescence assays using DAF-2 DA, whose signal was drastically reduced in the presence of the nitric oxide synthase inhibitor N omega-Nitro-L-arginine methyl ester (L-NAME). These results were confirmed by quantitative chemiluminescent determination of the intracellular levels of nitric oxide-derived products. A putative nitric oxide synthase (NOS) activity was detected throughout sporulation, and this enzyme activity decreased significantly when L-NAME and 1-[2-(Trifluoromethyl)phenyl]imidazole (TRIM) were added to the assays. NOS assays carried out in the presence of EGTA showed decreased enzyme activity, suggesting the involvement of calcium ions in enzyme activation. Additionally, expressed sequence tags (ESTs) encoding putative guanylyl cyclases and a cGMP-phosphodiesterase were found in B. emersonii EST database (http://blasto.iq.usp.br), and the mRNA levels of the corresponding genes were observed to increase during sporulation. Altogether, data presented here revealed the presence and expression of guanylyl cyclase and cGMP phosphodiesterase genes in B. emersonii and provided evidence of a Ca(2+)-(center dot)NO-cGMP signaling pathway playing a role in zoospore biogenesis. (C) 2009 Elsevier Inc. All rights reserved.
dc.languageeng
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE
dc.relationFungal Genetics and Biology
dc.rightsCopyright ACADEMIC PRESS INC ELSEVIER SCIENCE
dc.rightsrestrictedAccess
dc.subjectCyclic GMP
dc.subjectODQ
dc.subjectGuanylyl cyclase
dc.subjectcGMP phosphodiesterase
dc.subjectNitric oxide
dc.subjectSporulation
dc.subjectCytodifferentiation
dc.subjectAquatic fungus
dc.titleEvidence of a Ca(2+)-(center dot)NO-cGMP signaling pathway controlling zoospore biogenesis in the aquatic fungus Blastocladiella emersonii
dc.typeArtículos de revistas


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