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      Pathogen‐induced expression of a blight tolerance transgene in American chestnut

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          Abstract

          American chestnut ( Castanea dentata) is a susceptible host of the invasive necrotrophic fungus Cryphonectria parasitica, which causes chestnut blight disease. The fungal pathogen attacks chestnut stems by invading wounded tissue and secreting oxalate. This process leads to the death of infected host cells and the formation of cankers, eventually girdling stems and killing the tree above the infections. To reduce damage caused by fungal oxalate, American chestnut has been genetically engineered to express a wheat oxalate oxidase ( OxO). This enzyme degrades the oxalate produced by the pathogen and confers elevated tolerance to Cryphonectria parasitica infection. We report new lines of transgenic American chestnut that have been developed with the win3.12 inducible promoter from poplar ( Populus deltoides) driving OxO expression. This promoter is responsive to both wounding and pathogen infection, with a low level of baseline expression. Targeted expression of OxO to wounded and infected tissue is sought as an alternative to constitutive expression for potential metabolic resource conservation and transgene stability over the long lifetime of a tree and over successive generations of breeding. Transgenic Castanea dentata lines harbouring the win3.12‐OxO construct were evaluated for transgene expression patterns and tolerance to chestnut blight infection. OxO transcript levels were low in uninfected plants, but robust infection‐induced expression levels were observed, with one transgenic line reaching levels comparable to those of previously characterized CaMV35S ‐OxO lines. In chestnut blight infection bioassays, win3.12‐OxO lines showed elevated disease tolerance similar to blight‐resistant Chinese chestnut ( Castanea mollissima) controls.

          Abstract

          In transgenic Castanea dentata, a promoter from Populus deltoides is strongly induced by Cryphonectria parasitica infection and effectively drives expression of the chestnut blight tolerance gene oxalate oxidase ( OxO).

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          Most cited references43

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          A Rapid and effective method for RNA extraction from different tissues of grapevine and other woody plants.

          RNA quality and integrity are critical for many studies in plant molecular biology. High-quality RNA extraction from grapevine and other woody plants is problematic due to the presence of polysaccharides, polyphenolics and other compounds that bind or co-precipitate with the RNA. To develop an optimised cetyltrimethylammonium bromide (CTAB)-based protocol, to reduce the time and cost of extraction without reducing quality and yield of RNA extracted from polysaccharide-rich tissues of several plants. Several changes were introduced to the original CTAB protocol. All centrifugation steps were carried out at 4 degrees C, the sample weight was decreased and the concentrations of PVP-40 and LiCl were increased reducing incubation time prior to RNA precipitation. This rapid CTAB protocol was compared with six different RNA extraction methods from three grapevine tissues, namely, in vitro plantlets, and leaves and mature canes from actively growing field vines. The rapid CTAB method gave high-quality RNA in only 3 h at low cost with efficiency equal to or higher than that obtained with other time-consuming and expensive protocols. The procedure was applied to RNA extraction from other grapevine tissues and other woody species including olive, lemon, poplar, chestnut, apple, pear, peach, cherry, apricot, plum and kiwi fruit. RNA of high quality could be isolated from all tissues and from all species. The study has shown that the improvement of a CTAB-based protocol allows the rapid isolation of high-quality RNA from grapevine and many woody species.
            • Record: found
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            How and Why Do Plants Inactivate Homologous (Trans)genes?

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              Promoter diversity in multigene transformation.

              Multigene transformation (MGT) is becoming routine in plant biotechnology as researchers seek to generate more complex and ambitious phenotypes in transgenic plants. Every nuclear transgene requires its own promoter, so when coordinated expression is required, the introduction of multiple genes leads inevitably to two opposing strategies: different promoters may be used for each transgene, or the same promoter may be used over and over again. In the former case, there may be a shortage of different promoters with matching activities, but repetitious promoter use may in some cases have a negative impact on transgene stability and expression. Using illustrative case studies, we discuss promoter deployment strategies in transgenic plants that increase the likelihood of successful and stable multiple transgene expression.

                Author and article information

                Contributors
                ehcarlso@syr.edu
                Journal
                Mol Plant Pathol
                Mol Plant Pathol
                10.1111/(ISSN)1364-3703
                MPP
                Molecular Plant Pathology
                John Wiley and Sons Inc. (Hoboken )
                1464-6722
                1364-3703
                28 November 2021
                March 2022
                : 23
                : 3 ( doiID: 10.1111/mpp.v23.3 )
                : 370-382
                Affiliations
                [ 1 ] Department of Environmental Biology SUNY College of Environmental Science and Forestry Syracuse New York USA
                Author notes
                [*] [* ] Correspondence

                Erik Carlson, Department of Environmental Biology, SUNY College of Environmental Science and Forestry, Syracuse, NY 13210, USA.

                Email: ehcarlso@ 123456syr.edu

                Author information
                https://orcid.org/0000-0002-0259-6499
                Article
                MPP13165
                10.1111/mpp.13165
                8828690
                34841616
                ed6fca57-e02b-49ab-bc8e-00adf101d867
                © 2021 The Authors. Molecular Plant Pathology published by British Society for Plant Pathology and John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 26 October 2021
                : 09 July 2021
                : 03 November 2021
                Page count
                Figures: 6, Tables: 3, Pages: 14, Words: 7479
                Funding
                Funded by: The American Chestnut Foundation
                Funded by: TheṣState of New York
                Funded by: Templeton World Charity Foundation, Inc. , doi 10.13039/501100011730;
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                March 2022
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.1.1 mode:remove_FC converted:09.02.2022

                Plant science & Botany
                blight tolerance,castanea dentata,cryphonectria parasitica,oxalate oxidase (oxo), win3.12 poplar promoter

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