Arabidopsis Basic Helix-Loop-Helix Transcription Factors MYC2, MYC3, and MYC4 Regulate Glucosinolate Biosynthesis, Insect Performance, and Feeding Behavior

Author:

Schweizer Fabian1,Fernández-Calvo Patricia2,Zander Mark3,Diez-Diaz Monica2,Fonseca Sandra2,Glauser Gaétan4,Lewsey Mathew G.35,Ecker Joseph R.356,Solano Roberto2,Reymond Philippe1

Affiliation:

1. Department of Plant Molecular Biology, University of Lausanne, CH-1015 Lausanne, Switzerland

2. Departamento de Genética Molecular de Plantas, Centro Nacional de Biotecnología–Consejo Superior de Investigaciones Científicas, Campus Universidad Autónoma, 28049 Madrid, Spain

3. Plant Biology Laboratory, The Salk Institute for Biological Studies, La Jolla, California 92037

4. Chemical Analytical Service of the Swiss Plant Science Web, University of Neuchâtel, 2009 Neuchatel, Switzerland

5. Genomic Analysis Laboratory, The Salk Institute for Biological Studies, La Jolla, California 92037

6. Howard Hughes Medical Institute, The Salk Institute for Biological Studies, La Jolla, California 92037

Abstract

Abstract Arabidopsis thaliana plants fend off insect attack by constitutive and inducible production of toxic metabolites, such as glucosinolates (GSs). A triple mutant lacking MYC2, MYC3, and MYC4, three basic helix-loop-helix transcription factors that are known to additively control jasmonate-related defense responses, was shown to have a highly reduced expression of GS biosynthesis genes. The myc2 myc3 myc4 (myc234) triple mutant was almost completely devoid of GS and was extremely susceptible to the generalist herbivore Spodoptera littoralis. On the contrary, the specialist Pieris brassicae was unaffected by the presence of GS and preferred to feed on wild-type plants. In addition, lack of GS in myc234 drastically modified S. littoralis feeding behavior. Surprisingly, the expression of MYB factors known to regulate GS biosynthesis genes was not altered in myc234, suggesting that MYC2/MYC3/MYC4 are necessary for direct transcriptional activation of GS biosynthesis genes. To support this, chromatin immunoprecipitation analysis showed that MYC2 binds directly to the promoter of several GS biosynthesis genes in vivo. Furthermore, yeast two-hybrid and pull-down experiments indicated that MYC2/MYC3/MYC4 interact directly with GS-related MYBs. This specific MYC–MYB interaction plays a crucial role in the regulation of defense secondary metabolite production and underlines the importance of GS in shaping plant interactions with adapted and nonadapted herbivores.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Plant Science

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