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  1. Article ; Online: Opposing functions of the plant TOPLESS gene family during SNC1-mediated autoimmunity.

    Garner, Christopher M / Spears, Benjamin J / Su, Jianbin / Cseke, Leland J / Smith, Samantha N / Rogan, Conner J / Gassmann, Walter

    PLoS genetics

    2021  Volume 17, Issue 2, Page(s) e1009026

    Abstract: Regulation of the plant immune system is important for controlling the specificity and amplitude of responses to pathogens and in preventing growth-inhibiting autoimmunity that leads to reductions in plant fitness. In previous work, we reported that ... ...

    Abstract Regulation of the plant immune system is important for controlling the specificity and amplitude of responses to pathogens and in preventing growth-inhibiting autoimmunity that leads to reductions in plant fitness. In previous work, we reported that SRFR1, a negative regulator of effector-triggered immunity, interacts with SNC1 and EDS1. When SRFR1 is non-functional in the Arabidopsis accession Col-0, SNC1 levels increase, causing a cascade of events that lead to autoimmunity phenotypes. Previous work showed that some members of the transcriptional co-repressor family TOPLESS interact with SNC1 to repress negative regulators of immunity. Therefore, to explore potential connections between SRFR1 and TOPLESS family members, we took a genetic approach that examined the effect of each TOPLESS member in the srfr1 mutant background. The data indicated that an additive genetic interaction exists between SRFR1 and two members of the TOPLESS family, TPR2 and TPR3, as demonstrated by increased stunting and elevated PR2 expression in srfr1 tpr2 and srfr1 tpr2 tpr3 mutants. Furthermore, the tpr2 mutation intensifies autoimmunity in the auto-active snc1-1 mutant, indicating a novel role of these TOPLESS family members in negatively regulating SNC1-dependent phenotypes. This negative regulation can also be reversed by overexpressing TPR2 in the srfr1 tpr2 background. Similar to TPR1 that positively regulates snc1-1 phenotypes by interacting with SNC1, we show here that TPR2 directly binds the N-terminal domain of SNC1. In addition, TPR2 interacts with TPR1 in vivo, suggesting that the opposite functions of TPR2 and TPR1 are based on titration of SNC1-TPR1 complexes by TPR2 or altered functions of a SNC1-TPR1-TPR2 complex. Thus, this work uncovers diverse functions of individual members of the TOPLESS family in Arabidopsis and provides evidence for the additive effect of transcriptional and post-transcriptional regulation of SNC1.
    MeSH term(s) Arabidopsis/genetics ; Arabidopsis/immunology ; Arabidopsis/metabolism ; Arabidopsis Proteins/genetics ; Arabidopsis Proteins/metabolism ; Autoimmunity/genetics ; Gene Expression Regulation, Plant/genetics ; Gene Expression Regulation, Plant/immunology ; Molecular Chaperones/genetics ; Molecular Chaperones/metabolism ; Mutation ; Plant Immunity/genetics ; Plants, Genetically Modified ; Up-Regulation
    Chemical Substances AT1G04130 protein, Arabidopsis ; Arabidopsis Proteins ; Molecular Chaperones ; SNC1 protein, Arabidopsis ; SRFR1 protein, Arabidopsis ; topless protein, Arabidopsis ; topless-related 1 protein, Arabidopsis
    Language English
    Publishing date 2021-02-23
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 2186725-2
    ISSN 1553-7404 ; 1553-7390
    ISSN (online) 1553-7404
    ISSN 1553-7390
    DOI 10.1371/journal.pgen.1009026
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Direct Regulation of the

    Spears, Benjamin J / Howton, T C / Gao, Fei / Garner, Christopher M / Mukhtar, M Shahid / Gassmann, Walter

    Molecular plant-microbe interactions : MPMI

    2019  Volume 32, Issue 5, Page(s) 540–549

    Abstract: One layer of the innate immune system allows plants to recognize pathogen-associated molecular patterns (PAMPS), activating a defense response known as PAMP-triggered immunity (PTI). Maintaining an active immune response, however, comes at the cost of ... ...

    Abstract One layer of the innate immune system allows plants to recognize pathogen-associated molecular patterns (PAMPS), activating a defense response known as PAMP-triggered immunity (PTI). Maintaining an active immune response, however, comes at the cost of plant growth and development; accordingly, optimization of the balance between defense and development is critical to plant fitness. The TEOSINTE BRANCHED1/CYCLOIDEA/PROLIFERATING CELL FACTOR (TCP) transcription factor family consists of well-characterized transcriptional regulators of plant development and morphogenesis. The three closely related class I TCP transcription factors TCP8, TCP14, and TCP15 have also been implicated in the regulation of effector-triggered immunity, but there has been no previous characterization of PTI-related phenotypes. To identify TCP targets involved in PTI, we screened a PAMP-induced gene promoter library in a yeast one-hybrid assay and identified interactions of these three TCPs with the
    MeSH term(s) Arabidopsis/immunology ; Arabidopsis Proteins/genetics ; Gene Expression Regulation, Plant ; Peptide Elongation Factor Tu/genetics ; Plant Immunity/genetics ; Transcription Factors/genetics
    Chemical Substances Arabidopsis Proteins ; Transcription Factors ; Peptide Elongation Factor Tu (EC 3.6.1.-)
    Language English
    Publishing date 2019-03-29
    Publishing country United States
    Document type Journal Article
    ZDB-ID 743331-1
    ISSN 1943-7706 ; 0894-0282
    ISSN (online) 1943-7706
    ISSN 0894-0282
    DOI 10.1094/MPMI-07-18-0201-FI
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Leaping into the Unknown World of

    Teixeira-Silva, Natália Sousa / Schaker, Patrícia Dayane Carvalho / Rody, Hugo Vianna Silva / Maia, Thiago / Garner, Christopher M / Gassmann, Walter / Monteiro-Vitorello, Claudia Barros

    Journal of fungi (Basel, Switzerland)

    2020  Volume 6, Issue 4

    Abstract: Sporisorium ... ...

    Abstract Sporisorium scitamineum
    Language English
    Publishing date 2020-12-04
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2784229-0
    ISSN 2309-608X ; 2309-608X
    ISSN (online) 2309-608X
    ISSN 2309-608X
    DOI 10.3390/jof6040339
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Direct Regulation of the EFR-Dependent Immune Response by Arabidopsis TCP Transcription Factors

    Spears, Benjamin J / Howton, T. C / Gao, Fei / Garner, Christopher M / Mukhtar, M. Shahid / Gassmann, Walter

    Molecular plant-microbe interactions. 2019 May, v. 32, no. 5

    2019  

    Abstract: One layer of the innate immune system allows plants to recognize pathogen-associated molecular patterns (PAMPS), activating a defense response known as PAMP-triggered immunity (PTI). Maintaining an active immune response, however, comes at the cost of ... ...

    Abstract One layer of the innate immune system allows plants to recognize pathogen-associated molecular patterns (PAMPS), activating a defense response known as PAMP-triggered immunity (PTI). Maintaining an active immune response, however, comes at the cost of plant growth and development; accordingly, optimization of the balance between defense and development is critical to plant fitness. The TEOSINTE BRANCHED1/CYCLOIDEA/PROLIFERATING CELL FACTOR (TCP) transcription factor family consists of well-characterized transcriptional regulators of plant development and morphogenesis. The three closely related class I TCP transcription factors TCP8, TCP14, and TCP15 have also been implicated in the regulation of effector-triggered immunity, but there has been no previous characterization of PTI-related phenotypes. To identify TCP targets involved in PTI, we screened a PAMP-induced gene promoter library in a yeast one-hybrid assay and identified interactions of these three TCPs with the EF-Tu RECEPTOR (EFR) promoter. The direct interactions between TCP8 and EFR were confirmed to require an intact TCP binding site in planta. A tcp8 tcp14 tcp15 triple mutant was impaired in EFR-dependent PTI and exhibited reduced levels of PATHOGENESIS-RELATED PROTEIN 2 and induction of EFR expression after elicitation with elf18 but also increased production of reactive oxygen species relative to Col-0. Our data support an increasingly complex role for TCPs at the nexus of plant development and defense.
    Keywords Arabidopsis ; active immunity ; binding sites ; genes ; immune response ; innate immunity ; morphogenesis ; mutants ; pathogen-associated molecular patterns ; pathogenesis-related proteins ; phenotype ; plant development ; transcription factors ; yeasts
    Language English
    Dates of publication 2019-05
    Size p. 540-549.
    Publishing place Molecular Plant-Microbe Interactions
    Document type Article
    ZDB-ID 743331-1
    ISSN 1943-7706 ; 0894-0282
    ISSN (online) 1943-7706
    ISSN 0894-0282
    DOI 10.1094/MPMI-07-18-0201-FI
    Database NAL-Catalogue (AGRICOLA)

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  5. Article ; Online: Express yourself: Transcriptional regulation of plant innate immunity.

    Garner, Christopher M / Kim, Sang Hee / Spears, Benjamin J / Gassmann, Walter

    Seminars in cell & developmental biology

    2016  Volume 56, Page(s) 150–162

    Abstract: The plant immune system is a complex network of components that function together to sense the presence and activity of potential biotic threats, and integrate these signals into an appropriate output, namely the transcription of genes that activate an ... ...

    Abstract The plant immune system is a complex network of components that function together to sense the presence and activity of potential biotic threats, and integrate these signals into an appropriate output, namely the transcription of genes that activate an immune response that is commensurate with the perceived threat. Given the variety of biotic threats a plant must face the immune response must be plastic, but because an immune response is costly to the plant in terms of energy expenditure and development it must also be under tight control. To meet these needs transcriptional control is exercised at multiple levels. In this article we will review some of the latest developments in understanding how the plant immune response is regulated at the level of transcription. New roles are being discovered for the long-studied WRKY and TGA transcription factor families, while additional critical defense functions are being attributed to TCPs and other transcription factors. Dynamically controlling access to DNA through post-translational modification of histones is emerging as an essential component of priming, maintaining, attenuating, and repressing transcription in response to biotic stress. Unsurprisingly, the plant's transcriptional response is targeted by pathogen effectors, and in turn resistance proteins stand guard over and participate in transcriptional regulation. Together, these multiple layers lead to the observed complexity of the plant transcriptional immune response, with different transcription factors or chromatin components playing a prominent role depending on the plant-pathogen interaction being studied.
    Language English
    Publishing date 2016-08
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 1312473-0
    ISSN 1096-3634 ; 1084-9521
    ISSN (online) 1096-3634
    ISSN 1084-9521
    DOI 10.1016/j.semcdb.2016.05.002
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: New clues in the nucleus: transcriptional reprogramming in effector-triggered immunity.

    Bhattacharjee, Saikat / Garner, Christopher M / Gassmann, Walter

    Frontiers in plant science

    2013  Volume 4, Page(s) 364

    Abstract: The robustness of plant effector-triggered immunity is correlated with massive alterations of the host transcriptome. Yet the molecular mechanisms that cause and underlie this reprogramming remain obscure. Here we will review recent advances in ... ...

    Abstract The robustness of plant effector-triggered immunity is correlated with massive alterations of the host transcriptome. Yet the molecular mechanisms that cause and underlie this reprogramming remain obscure. Here we will review recent advances in deciphering nuclear functions of plant immune receptors and of associated proteins. Important open questions remain, such as the identities of the primary transcription factors involved in control of effector-triggered immune responses, and indeed whether this can be generalized or whether particular effector-resistance protein interactions impinge on distinct sectors in the transcriptional response web. Multiple lines of evidence have implicated WRKY transcription factors at the core of responses to microbe-associated molecular patterns and in intersections with effector-triggered immunity. Recent findings from yeast two-hybrid studies suggest that members of the TCP transcription factor family are targets of several effectors from diverse pathogens. Additional transcription factor families that are directly or indirectly involved in effector-triggered immunity are likely to be identified.
    Language English
    Publishing date 2013-09-13
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2613694-6
    ISSN 1664-462X
    ISSN 1664-462X
    DOI 10.3389/fpls.2013.00364
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: The bacterial type III-secreted protein AvrRps4 is a bipartite effector.

    Halane, Morgan K / Kim, Sang Hee / Spears, Benjamin J / Garner, Christopher M / Rogan, Conner J / Okafor, Elizabeth C / Su, Jianbin / Bhattacharjee, Saikat / Gassmann, Walter

    PLoS pathogens

    2018  Volume 14, Issue 3, Page(s) e1006984

    Abstract: Bacterial effector proteins secreted into host plant cells manipulate those cells to the benefit of the pathogen, but effector-triggered immunity (ETI) occurs when effectors are recognized by host resistance proteins. The RPS4/RRS1 pair recognizes the ... ...

    Abstract Bacterial effector proteins secreted into host plant cells manipulate those cells to the benefit of the pathogen, but effector-triggered immunity (ETI) occurs when effectors are recognized by host resistance proteins. The RPS4/RRS1 pair recognizes the Pseudomonas syringae pv. pisi effector AvrRps4. AvrRps4 is processed in planta into AvrRps4N (133 amino acids), homologous to the N-termini of other effectors including the native P. syringae pv. tomato strain DC3000 effector HopK1, and AvrRps4C (88 amino acids). Previous data suggested that AvrRps4C alone is necessary and sufficient for resistance when overexpressed in heterologous systems. We show that delivering AvrRps4C from DC3000, but not from a DC3000 hopK1- strain, triggers resistance in the Arabidopsis accession Col-0. Delivering AvrRps4C in tandem with AvrRps4N, or as a chimera with HopK1N, fully complements AvrRps4-triggered immunity. AvrRps4N in the absence of AvrRps4C enhances virulence in Col-0. In addition, AvrRps4N triggers a hypersensitive response in lettuce that is attenuated by coexpression of AvrRps4C, further supporting the role of AvrRps4N as a bona fide effector domain. Based on these results we propose that evolutionarily, fusion of AvrRps4C to AvrRps4N may have counteracted recognition of AvrRps4N, and that the plant RPS4/RRS1 resistance gene pair was selected as a countermeasure. We conclude that AvrRps4 represents an unusual chimeric effector, with recognition in Arabidopsis by RPS4/RRS1 requiring the presence of both processed effector moieties.
    MeSH term(s) Arabidopsis/immunology ; Arabidopsis/metabolism ; Arabidopsis/microbiology ; Arabidopsis Proteins/genetics ; Arabidopsis Proteins/metabolism ; Bacterial Proteins/secretion ; Gene Expression Regulation, Plant ; Plant Diseases/immunology ; Plant Diseases/microbiology ; Pseudomonas syringae/pathogenicity ; Virulence
    Chemical Substances Arabidopsis Proteins ; Bacterial Proteins
    Language English
    Publishing date 2018
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2205412-1
    ISSN 1553-7374 ; 1553-7366
    ISSN (online) 1553-7374
    ISSN 1553-7366
    DOI 10.1371/journal.ppat.1006984
    Database MEDical Literature Analysis and Retrieval System OnLINE

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