TheSUD1Gene Encodes a Putative E3 Ubiquitin Ligase and Is a Positive Regulator of 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase Activity inArabidopsis

Author:

Doblas Verónica G.1,Amorim-Silva Vítor2,Posé David1,Rosado Abel1,Esteban Alicia1,Arró Montserrat34,Azevedo Herlander2,Bombarely Aureliano1,Borsani Omar5,Valpuesta Victoriano1,Ferrer Albert34,Tavares Rui M.2,Botella Miguel A.1

Affiliation:

1. Instituto de Hortofruticultura Subtropical y Mediterránea, Universidad de Málaga–Consejo Superior de Investigaciones Científicas, Departamento de Biología Molecular y Bioquímica, Facultad de Ciencias, Universidad de Málaga, 29071 Malaga, Spain

2. Center for Biodiversity, Functional and Integrative Genomics, Plant Functional Biology Center, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal

3. Department of Molecular Genetics, Centre for Research in Agricultural Genomics (Consejo Superior de Investigaciones Científicas-Institut de Recerca i Tecnologia Agroalimentàries-Universidad Autónoma de Barcelona-Universidad de Barcelona), Bellaterra-Cerdanyola del Vallés, 08193 Barcelona, Spain

4. Department of Biochemistry and Molecular Biology, Faculty of Pharmacy, University of Barcelona, 08028 Barcelona, Spain

5. Laboratorio de Bioquímica, Departamento de Biología Vegetal, Facultad de Agronomía, Universidad de la República, Montevideo CP12900, Uruguay

Abstract

AbstractThe 3-hydroxy-3-methylglutaryl-CoA reductase (HMGR) enzyme catalyzes the major rate-limiting step of the mevalonic acid (MVA) pathway from which sterols and other isoprenoids are synthesized. In contrast with our extensive knowledge of the regulation of HMGR in yeast and animals, little is known about this process in plants. To identify regulatory components of the MVA pathway in plants, we performed a genetic screen for second-site suppressor mutations of the Arabidopsis thaliana highly drought-sensitive drought hypersensitive2 (dry2) mutant that shows decreased squalene epoxidase activity. We show that mutations in SUPPRESSOR OF DRY2 DEFECTS1 (SUD1) gene recover most developmental defects in dry2 through changes in HMGR activity. SUD1 encodes a putative E3 ubiquitin ligase that shows sequence and structural similarity to yeast Degradation of α factor (Doα10) and human TEB4, components of the endoplasmic reticulum–associated degradation C (ERAD-C) pathway. While in yeast and animals, the alternative ERAD-L/ERAD-M pathway regulates HMGR activity by controlling protein stability, SUD1 regulates HMGR activity without apparent changes in protein content. These results highlight similarities, as well as important mechanistic differences, among the components involved in HMGR regulation in plants, yeast, and animals.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Plant Science

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