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231224s2012 xx |||||o 00| ||eng c |
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|a 10.1093/jxb/ers029
|2 doi
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|a pubmed24n1405.xml
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|a (DE-627)NLM216436621
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|a (NLM)22442421
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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|a Andriunas, Felicity A
|e verfasserin
|4 aut
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|a Reactive oxygen species form part of a regulatory pathway initiating trans-differentiation of epidermal transfer cells in Vicia faba cotyledons
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|c 2012
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
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|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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|a Date Completed 23.11.2012
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|a Date Revised 12.05.2024
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Various cell types can trans-differentiate to a transfer cell (TC) morphology characterized by deposition of polarized ingrowth walls comprised of a uniform layer on which wall ingrowths (WIs) develop. WIs form scaffolds supporting amplified plasma membrane areas enriched in transporters conferring a cellular capacity for high rates of nutrient exchange across apo- and symplasmic interfaces. The hypothesis that reactive oxygen species (ROS) are a component of the regulatory pathway inducing ingrowth wall formation was tested using Vicia faba cotyledons. Vicia faba cotyledons offer a robust experimental model to examine TC induction as, on being placed into culture, their adaxial epidermal cells rapidly (hours) form ingrowth walls on their outer periclinal walls. These are readily visualized by electron microscopy, and epidermal peels of their trans-differentiating cells allow measures of cell-specific gene expression. Ingrowth wall formation responded inversely to pharmacological manipulation of ROS levels, indicating that a flavin-containing enzyme (NADPH oxidase) and superoxide dismutase cooperatively generate a regulatory H(2)O(2) signature. Extracellular H(2)O(2) fluxes peaked prior to the appearance of WIs and were followed by a slower rise in H(2)O(2) flux that occurred concomitantly, and co-localized, with ingrowth wall formation. De-localizing the H(2)O(2) signature caused a corresponding de-localization of cell wall deposition. Temporal and epidermal cell-specific expression profiles of VfrbohA and VfrbohC coincided with those of extracellular H(2)O(2) production and were regulated by cross-talk with ethylene. It is concluded that H(2)O(2) functions, downstream of ethylene, to activate cell wall biosynthesis and direct polarized deposition of a uniform wall on which WIs form
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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a Plant Proteins
|2 NLM
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|a Reactive Oxygen Species
|2 NLM
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|a Superoxide Dismutase
|2 NLM
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|a EC 1.15.1.1
|2 NLM
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|a NADPH Oxidases
|2 NLM
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|a EC 1.6.3.-
|2 NLM
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| 700 |
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|a Zhang, Hui-Ming
|e verfasserin
|4 aut
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|a Xia, Xue
|e verfasserin
|4 aut
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| 700 |
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|a Offler, Christina E
|e verfasserin
|4 aut
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|a McCurdy, David W
|e verfasserin
|4 aut
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| 700 |
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|a Patrick, John W
|e verfasserin
|4 aut
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| 773 |
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|i Enthalten in
|t Journal of experimental botany
|d 1985
|g 63(2012), 10 vom: 21. Juni, Seite 3617-29
|w (DE-627)NLM098182706
|x 1460-2431
|7 nnns
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| 773 |
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|g volume:63
|g year:2012
|g number:10
|g day:21
|g month:06
|g pages:3617-29
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|u http://dx.doi.org/10.1093/jxb/ers029
|3 Volltext
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