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Functional characterization of petunia petal senescence related proteins by virus-induced gene silencing

Please use this identifier to cite or link to this item: http://hdl.handle.net/1811/24703

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dc.contributor Francis, David
dc.contributor Willard, Belinda
dc.contributor Kinter, Michael
dc.contributor.advisor Jones, Michelle L.
dc.creator Bai, Shuangyi
dc.date.accessioned 2007-04-02T13:26:53Z
dc.date.available 2007-04-02T13:26:53Z
dc.date.issued 2007-04-02T13:26:53Z
dc.identifier.uri http://hdl.handle.net/1811/24703
dc.description.abstract The senescence of vegetative and floral tissues can have a detrimental impact on the quality and subsequent value of agricultural and horticultural crops. Pollination, one of the key stimuli of senescence, can trigger and accelerate flower senescence and nutrient recycling. To profile protein expression during flower senescence, we used a proteomic approach to identify components of the senescence program in Petunia x hybrida cv Mitchell Diploid petals. Two- dimensional gel electrophoresis (2DE) was used to identify those proteins that were differentially expressed in nonsenescing (unpollinated) and senescing (pollinated) corollas. Proteins that increased in abundance during petal senescence are mainly involved in stress or defense responses, carbohydrate and energy metabolism, and other catabolic processes including proteolysis, nuclei acid, cell wall and lipid degradation. Since virus-induced gene silencing (VIGS) is a high throughput transient approach to analyze gene function, we are employing VIGS to further investigate the function of the senescence up regulated proteins. A fragment of the petunia chalcone synthase gene (CHS) and a fragment of the target gene will be ligated in tandem into the TRV2 vector. Both Agroinfiltration and Agrodrench can induce high efficiency gene silencing in petunia flowers. Currently we are studying the function of two proteins. One is a nuclease that is up regulated in senescing petals. Its molecular weight is very close to that of PhNUC1 whose biochemical characterization has been previously studied by the Jones lab. Another protein is beta-D-xylosidase, which is likely to be related to cell wall disassembly and loosening. This is a highly abundant protein, whose full-length, N-terminal and C-terminal truncated forms were all up regulated during petal senescence. It indicated that this protein might be activated after post-translational modification or processing during petal senescence. en
dc.description.sponsorship OARDC Research Enhancement Competitive Grants Program en
dc.description.sponsorship The Fred C. Gloeckner Foundation en
dc.description.sponsorship The Ohio State University D.C. Kiplinger Endowment en
dc.format.extent 203363 bytes
dc.format.mimetype application/pdf
dc.language.iso en_US en
dc.relation.ispartofseries Horticulture and Crop Science. Graduate student poster competition, 2007 en
dc.subject Proteomics en
dc.subject flower senescence en
dc.title Functional characterization of petunia petal senescence related proteins by virus-induced gene silencing en
dc.type Presentation en