Modulating and monitoring mapk activity during programmed cell death in pollen

DC ElementWertSprache
dc.contributor.authorLi, S.
dc.contributor.authorFranklin-Tong, V.E.
dc.date.accessioned2021-12-23T16:31:27Z-
dc.date.available2021-12-23T16:31:27Z-
dc.date.issued2011
dc.identifier.isbn9781617792632
dc.identifier.issn10643745
dc.identifier.urihttps://osnascholar.ub.uni-osnabrueck.de/handle/unios/17091-
dc.description.abstractSignal transduction through mitogen-activated protein kinase (MAPK) cascades regulates many cellular responses. One example of a stimulus-mediated MAPK signaling network in plants is the self-incompatibility (SI) response in Papaver rhoeas, which represents an important mechanism to prevent self-fertilization. This involves interaction of pistil S-locus determinants with a pollen receptor in an incompatible interaction, resulting in a Ca2+-dependent signaling network involving activation of a MAPK, p56, and stimulation of several caspase-like activities, resulting in programmed cell death (PCD). MAPK inhibitors provide a useful tool to dissect these mechanisms and distinguish their regulation by different signaling pathways. U0126 is a potent, noncompetitive, and specific inhibitor of MAPK signaling pathways that result in the inhibition of MAPK activation. Here, we describe the use of this drug in combination with a TEY (threonine–glutamic acid–tyrosine) antibody to alter and monitor MAPK activation, together with a range of markers for PCD to implicate a role for MAPK activation in signaling to PCD in pollen tubes. These techniques may be potentially adapted for use in other plant tissues to investigate MAPK activation in other physiologically relevant systems. © Springer Science+Business Media, LLC 2011.
dc.description.sponsorshipRoyal SocietyRoyal Society; The authors would like to thank Kim Osman, Chris Franklin, Barend de Graaf, Steve Thomas, and Maurice Bosch for helpful comments and technical assistance. This work was supported by the Royal Society and the Biotechnology and Biological Sciences Research Council (BBSRC).
dc.language.isoen
dc.publisherHumana Press Inc.
dc.relation.ispartofMethods in Molecular Biology
dc.subject1,4 diamino 1,4 bis(2 aminophenylthio) 2,3 dicyanobutadiene, 109511-58-2
dc.subjectcaspase 3, 169592-56-7
dc.subjectmitogen activated protein kinase, 142243-02-5
dc.subjectnicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase, 58319-92-9
dc.subjectAntibodies, Neutralizing
dc.subjectButadienes
dc.subjectCaspase 3, 3.4.22.-
dc.subjectMitogen-Activated Protein Kinases, 2.7.11.24
dc.subjectNitriles
dc.subjectPoly(ADP-ribose) Polymerases, 2.4.2.30
dc.subjectProtein Kinase Inhibitors
dc.subjectU 0126
dc.subject1,3 butadiene derivative
dc.subject1,4 diamino 1,4 bis(2 aminophenylthio) 2,3 dicyanobutadiene
dc.subjectApoptosis
dc.subjectarticle
dc.subjectButadienes
dc.subjectCaspase 3
dc.subjectCaspase-3-like activity
dc.subjectDNA Fragmentation
dc.subjectdrug antagonism
dc.subjectdrug effect
dc.subjectEnzyme Activation
dc.subjectenzyme assay
dc.subjectEnzyme Assays
dc.subjectenzymology
dc.subjectimmunology
dc.subjectMAPK
dc.subjectmetabolism
dc.subjectmethodology
dc.subjectmitogen activated protein kinase
dc.subjectMitogen-Activated Protein Kinases
dc.subjectneutralizing antibody
dc.subjectnicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase
dc.subjectnitrile
dc.subjectNitriles
dc.subjectPapaver
dc.subjectPapaver rhoeas
dc.subjectPCD
dc.subjectPollen
dc.subjectpollen, Antibodies, Neutralizing
dc.subjectPoly(ADP-ribose) Polymerases
dc.subjectprotein kinase inhibitor, apoptosis
dc.subjectProtein Kinase Inhibitors, Papaver rhoeas
dc.subjectSelf-incompatibility
dc.subjectU0126
dc.titleModulating and monitoring mapk activity during programmed cell death in pollen
dc.typebook part
dc.identifier.doi10.1007/978-1-61779-264-9_9
dc.identifier.pmid21837566
dc.identifier.scopus2-s2.0-80054726036
dc.identifier.urlhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-80054726036&doi=10.1007%2f978-1-61779-264-9_9&partnerID=40&md5=14fb3327ca001e0681ca265c1350759f
dc.description.volume779
dc.description.startpage165
dc.description.endpage183
dcterms.isPartOf.abbreviationMethods Mol. Biol.
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