Identification and Characterization of ANAC042, a Transcription Factor Family Gene Involved in the Regulation of Camalexin Biosynthesis in Arabidopsis

Camalexin is the major phytoalexin in Arabidopsis. An almost complete set of camalexin biosynthetic enzymes have been elucidated but only limited information is available regarding molecular mechanisms regulating camalexin biosynthesis. Here, we demonstrate that ANAC042, a member of the NAM, ATAF1/2...

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Main Authors: Hirohisa Saga, Takumi Ogawa, Kosuke Kai, Hideyuki Suzuki, Yoshiyuki Ogata, Nozomu Sakurai, Daisuke Shibata, Daisaku Ohta
Format: Article
Language:English
Published: The American Phytopathological Society 2012-05-01
Series:Molecular Plant-Microbe Interactions
Online Access:https://apsjournals.apsnet.org/doi/10.1094/MPMI-09-11-0244
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author Hirohisa Saga
Takumi Ogawa
Kosuke Kai
Hideyuki Suzuki
Yoshiyuki Ogata
Nozomu Sakurai
Daisuke Shibata
Daisaku Ohta
author_facet Hirohisa Saga
Takumi Ogawa
Kosuke Kai
Hideyuki Suzuki
Yoshiyuki Ogata
Nozomu Sakurai
Daisuke Shibata
Daisaku Ohta
author_sort Hirohisa Saga
collection DOAJ
description Camalexin is the major phytoalexin in Arabidopsis. An almost complete set of camalexin biosynthetic enzymes have been elucidated but only limited information is available regarding molecular mechanisms regulating camalexin biosynthesis. Here, we demonstrate that ANAC042, a member of the NAM, ATAF1/2, and CUC2 (NAC) transcription factor family genes, is involved in camalexin biosynthesis induction. T-DNA insertion mutants of ANAC042 failed to accumulate camalexin at the levels achieved in the wild type, and were highly susceptible to Alternaria brassicicola infection. The camalexin biosynthetic genes CYP71A12, CYP71A13, and CYP71B15/PAD3 were not fully induced in the mutants, indicating that the camalexin defects were at least partly a result of reduced expression levels of these P450 genes. β-Glucuronidase (GUS)-reporter assays demonstrated tissue-specific induction of ANAC042 in response to differential pathogen infections. Bacterial flagellin (Flg22) induced ANAC042 expression in the root-elongation zone, the camalexin biosynthetic site, and the induction was abolished in the presence of either a general kinase inhibitor (K252a), a Ca2+-chelator (BAPTA), or methyl jasmonate. The GUS-reporter assay revealed repression of the Flg22-dependent ANAC042 expression in the ethylene-insensitive ein2-1 background but not in sid2-2 plants defective for salicylic acid biosynthesis. We discuss ANAC042 as a key transcription factor involved in previously unknown regulatory mechanisms to induce phytoalexin biosynthesis in Arabidopsis.
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spelling doaj.art-ad13eb725af946178fce2615c865e6d02022-12-22T03:02:30ZengThe American Phytopathological SocietyMolecular Plant-Microbe Interactions0894-02821943-77062012-05-0125568469610.1094/MPMI-09-11-0244Identification and Characterization of ANAC042, a Transcription Factor Family Gene Involved in the Regulation of Camalexin Biosynthesis in ArabidopsisHirohisa SagaTakumi OgawaKosuke KaiHideyuki SuzukiYoshiyuki OgataNozomu SakuraiDaisuke ShibataDaisaku OhtaCamalexin is the major phytoalexin in Arabidopsis. An almost complete set of camalexin biosynthetic enzymes have been elucidated but only limited information is available regarding molecular mechanisms regulating camalexin biosynthesis. Here, we demonstrate that ANAC042, a member of the NAM, ATAF1/2, and CUC2 (NAC) transcription factor family genes, is involved in camalexin biosynthesis induction. T-DNA insertion mutants of ANAC042 failed to accumulate camalexin at the levels achieved in the wild type, and were highly susceptible to Alternaria brassicicola infection. The camalexin biosynthetic genes CYP71A12, CYP71A13, and CYP71B15/PAD3 were not fully induced in the mutants, indicating that the camalexin defects were at least partly a result of reduced expression levels of these P450 genes. β-Glucuronidase (GUS)-reporter assays demonstrated tissue-specific induction of ANAC042 in response to differential pathogen infections. Bacterial flagellin (Flg22) induced ANAC042 expression in the root-elongation zone, the camalexin biosynthetic site, and the induction was abolished in the presence of either a general kinase inhibitor (K252a), a Ca2+-chelator (BAPTA), or methyl jasmonate. The GUS-reporter assay revealed repression of the Flg22-dependent ANAC042 expression in the ethylene-insensitive ein2-1 background but not in sid2-2 plants defective for salicylic acid biosynthesis. We discuss ANAC042 as a key transcription factor involved in previously unknown regulatory mechanisms to induce phytoalexin biosynthesis in Arabidopsis.https://apsjournals.apsnet.org/doi/10.1094/MPMI-09-11-0244
spellingShingle Hirohisa Saga
Takumi Ogawa
Kosuke Kai
Hideyuki Suzuki
Yoshiyuki Ogata
Nozomu Sakurai
Daisuke Shibata
Daisaku Ohta
Identification and Characterization of ANAC042, a Transcription Factor Family Gene Involved in the Regulation of Camalexin Biosynthesis in Arabidopsis
Molecular Plant-Microbe Interactions
title Identification and Characterization of ANAC042, a Transcription Factor Family Gene Involved in the Regulation of Camalexin Biosynthesis in Arabidopsis
title_full Identification and Characterization of ANAC042, a Transcription Factor Family Gene Involved in the Regulation of Camalexin Biosynthesis in Arabidopsis
title_fullStr Identification and Characterization of ANAC042, a Transcription Factor Family Gene Involved in the Regulation of Camalexin Biosynthesis in Arabidopsis
title_full_unstemmed Identification and Characterization of ANAC042, a Transcription Factor Family Gene Involved in the Regulation of Camalexin Biosynthesis in Arabidopsis
title_short Identification and Characterization of ANAC042, a Transcription Factor Family Gene Involved in the Regulation of Camalexin Biosynthesis in Arabidopsis
title_sort identification and characterization of anac042 a transcription factor family gene involved in the regulation of camalexin biosynthesis in arabidopsis
url https://apsjournals.apsnet.org/doi/10.1094/MPMI-09-11-0244
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