Abstract

Plant sterols are structural components of cell membranes that provide rigidity, permeability, and regional identity to membranes. Sterols are also the precursors to the brassinosteroid signaling molecules. Evidence is accumulating that specific sterols have roles in pattern formation during development. COTYLEDON VASCULAR PATTERNING1 (CVP1) encodes C-24 STEROL METHYLTRANSFERASE2 (SMT2), one of three SMTs in Arabidopsis (Arabidopsis thaliana). SMT2 and SMT3, which also encodes a C-24 SMT, catalyze the reaction that distinguishes the synthesis of structural sterols from signaling brassinosteroid derivatives and are highly regulated. The deficiency of SMT2 in the cvp1 mutant results in moderate developmental defects, including aberrant cotyledon vein patterning, serrated floral organs, and reduced stature, but plants are viable, suggesting that SMT3 activity can substitute for the loss of SMT2. To test the distinct developmental roles of SMT2 and SMT3, we identified a transcript null smt3 mutant. Although smt3 single mutants appear wild type, cvp1 smt3 double mutants show enhanced defects relative to cvp1 mutants, such as discontinuous cotyledon vein pattern, and produce novel phenotypes, including defective root growth, loss of apical dominance, sterility, and homeotic floral transformations. These phenotypes are correlated with major alterations in the profiles of specific sterols but without significant alterations to brassinosteroid profiles. The alterations to sterol profiles in cvp1 mutants affect auxin response, demonstrated by weak auxin insensitivity, enhanced axr1 auxin resistance, ectopically expressed DR5:beta-glucuronidase in developing embryos, and defective response to auxin-inhibited PIN2-green fluorescent protein endocytosis. We discuss the developmental roles of sterols implied by these results.

Highlights

  • Plant sterols are structural components of cell membranes that provide rigidity, permeability, and regional identity to membranes

  • As has been demonstrated previously with cvp1 and smt1 mutants, SMT1 and STEROL METHYLTRANSFERASE2 (SMT2) transcript levels were reduced in the smt3 mutant, suggesting that STEROL METHYLTRANSFERASEs (SMTs) transcription may be regulated through a sterol feedback mechanism (Diener et al, 2000; Carland et al, 2002)

  • We show that in the cvp1 and smt3 mutants, the sterol content is dramatically affected without disrupting BR levels

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Summary

Introduction

Plant sterols are structural components of cell membranes that provide rigidity, permeability, and regional identity to membranes. Mutants including sterol methyltransferase (smt; called cephalopod [cph]), fackel (fk; allelic to hydra2 [hyd2]), hyd, cyclopropylsterol isomerase (cpi), and cotyledon vascular pattern (cvp1) reveal roles for sterols in embryo, vein, shoot and root patterning, cell expansion, polarity and proliferation, fertility, cellulose level maintenance, gravitropism, and hormone signaling (Diener et al, 2000; Jang et al, 2000; Schrick et al, 2000, 2002, 2004a; Carland et al, 2002; Peng et al, 2002; Souter et al, 2002, 2004; Willemsen et al, 2003; Men et al, 2008). The dwarf phenotypes of BR biosynthetic mutants, including dwarf7/sterol (dwf7/ste1) and dwf1/dim, are rescued by exogenous brassinolide (BL) application (Choe et al, 1999a, 1999b)

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