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1.
Planta ; 251(4): 75, 2020 Mar 07.
Artigo em Inglês | MEDLINE | ID: mdl-32146566

RESUMO

MAIN CONCLUSION: Carbonic anhydrases CA1 and CA4 attenuate plant immunity and can contribute to altered disease resistance levels in response to changing atmospheric CO2 conditions. ß-Carbonic anhydrases (CAs) play an important role in CO2 metabolism and plant development, but have also been implicated in plant immunity. Here we show that the bacterial pathogen Pseudomonas syringae and application of the microbe-associated molecular pattern (MAMP) flg22 repress CA1 and CA4 gene expression in Arabidopsis thaliana. Using the CA double-mutant ca1ca4, we provide evidence that CA1 and CA4 play an attenuating role in pathogen- and flg22-triggered immune responses. In line with this, ca1ca4 plants exhibited enhanced resistance against P. syringae, which was accompanied by an increased expression of the defense-related genes FRK1 and ICS1. Under low atmospheric CO2 conditions (150 ppm), when CA activity is typically low, the levels of CA1 transcription and resistance to P. syringae in wild-type Col-0 were similar to those observed in ca1ca4. However, under ambient (400 ppm) and elevated (800 ppm) atmospheric CO2 conditions, CA1 transcription was enhanced and resistance to P. syringae reduced. Together, these results suggest that CA1 and CA4 attenuate plant immunity and that differential CA gene expression in response to changing atmospheric CO2 conditions contribute to altered disease resistance levels.


Assuntos
Proteínas de Arabidopsis/metabolismo , Dióxido de Carbono/metabolismo , Anidrases Carbônicas/metabolismo , Doenças das Plantas , Arabidopsis/genética , Arabidopsis/microbiologia , Proteínas de Arabidopsis/genética , Anidrases Carbônicas/genética , Resistência à Doença , Imunidade Vegetal , Pseudomonas syringae/metabolismo , Espécies Reativas de Oxigênio/metabolismo , Fatores de Transcrição/genética , Fatores de Transcrição/metabolismo , Transcriptoma
2.
Plant Cell ; 29(9): 2086-2105, 2017 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-28827376

RESUMO

Jasmonic acid (JA) is a critical hormonal regulator of plant growth and defense. To advance our understanding of the architecture and dynamic regulation of the JA gene regulatory network, we performed a high-resolution RNA-seq time series of methyl JA-treated Arabidopsis thaliana at 15 time points over a 16-h period. Computational analysis showed that methyl JA (MeJA) induces a burst of transcriptional activity, generating diverse expression patterns over time that partition into distinct sectors of the JA response targeting specific biological processes. The presence of transcription factor (TF) DNA binding motifs correlated with specific TF activity during temporal MeJA-induced transcriptional reprogramming. Insight into the underlying dynamic transcriptional regulation mechanisms was captured in a chronological model of the JA gene regulatory network. Several TFs, including MYB59 and bHLH27, were uncovered as early network components with a role in pathogen and insect resistance. Analysis of subnetworks surrounding the TFs ORA47, RAP2.6L, MYB59, and ANAC055, using transcriptome profiling of overexpressors and mutants, provided insights into their regulatory role in defined modules of the JA network. Collectively, our work illuminates the complexity of the JA gene regulatory network, pinpoints and validates previously unknown regulators, and provides a valuable resource for functional studies on JA signaling components in plant defense and development.


Assuntos
Arabidopsis/genética , Ciclopentanos/metabolismo , Redes Reguladoras de Genes , Oxilipinas/metabolismo , Acetatos/farmacologia , Animais , Sequência de Bases , Ciclopentanos/farmacologia , DNA de Plantas/metabolismo , Perfilação da Expressão Gênica , Regulação da Expressão Gênica de Plantas/efeitos dos fármacos , Redes Reguladoras de Genes/efeitos dos fármacos , Genes de Plantas , Insetos/fisiologia , Família Multigênica , Motivos de Nucleotídeos/genética , Oxilipinas/farmacologia , Fatores de Tempo , Fatores de Transcrição/metabolismo , Transcrição Gênica/efeitos dos fármacos
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