Please use this identifier to cite or link to this item: https://doi.org/10.1093/jxb/erl229
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dc.titleCharacterization of two ethylene receptors PhERS1 and PhETR2 from petunia: PhETR2 regulates timing of anther dehiscence
dc.contributor.authorWang, Y.
dc.contributor.authorKumar, P.P.
dc.date.accessioned2014-10-27T08:23:43Z
dc.date.available2014-10-27T08:23:43Z
dc.date.issued2007-02
dc.identifier.citationWang, Y., Kumar, P.P. (2007-02). Characterization of two ethylene receptors PhERS1 and PhETR2 from petunia: PhETR2 regulates timing of anther dehiscence. Journal of Experimental Botany 58 (3) : 533-544. ScholarBank@NUS Repository. https://doi.org/10.1093/jxb/erl229
dc.identifier.issn00220957
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/100252
dc.description.abstractTwo cDNAs (PhERS1 and PhETR2) encoding ethylene receptor homologues were cloned and characterized from petunia. Genomic Southern blot analysis revealed that small families of PhERS1-related and PhETR2-related genes exist in petunia. PhERS1 and PhETR2 are constitutively expressed in stem, flower bud, flower, and roots, with a very low level in leaves. High levels of both PhERS1 and PhETR2 transcripts were detectable in petunia leaves treated with exogenous ethylene, while only PhETR2 mRNA increased after wounding and salt treatment. Arabidopsis plants transformed with a site-mutated PhERS1 in the potential ethylene-binding domain exhibited partial ethylene insensitivity, suggesting that the function of this domain is conserved in the two species. Transgenic petunia plants with decreased PhERS1 expression caused by double-stranded RNA inhibition (dsRNAi) exhibited the wild-type phenotype, but showed increased mRNA levels of PhETR2. This suggests functional compensation between the two genes. Antisense suppression of PhETR2 in petunia led to stomium degeneration and anther dehiscence before anthesis, indicating that PhETR2 regulates synchronization of anther dehiscence with flower opening. Tandem affinity purification (TAP)-tagged PhERS1 was transiently expressed in Nicotiana benthamiana leaves. Gel filtration analysis showed that TAP-PhERS1 forms a ∼300 kDa protein complex in vivo. © The Author [2006]. Published by Oxford University Press [on behalf of the Society for Experimental Biology]. All rights reserved.
dc.sourceScopus
dc.subjectAnther dehiscence
dc.subjectPetunia
dc.subjectSite-mutated ethylene receptor
dc.subjectTAP tag
dc.typeArticle
dc.contributor.departmentBIOLOGICAL SCIENCES
dc.description.doi10.1093/jxb/erl229
dc.description.sourcetitleJournal of Experimental Botany
dc.description.volume58
dc.description.issue3
dc.description.page533-544
dc.description.codenJEBOA
dc.identifier.isiut000244428400015
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