Plant Physiol, September 2002, Vol. 130, pp. 303-311
Sterol C-24 Methyltransferase Type 1 Controls the Flux of Carbon
into Sterol Biosynthesis in Tobacco Seed
Niklas
Holmberg,*
Mark
Harker,
Carl L.
Gibbard,
Andrew D.
Wallace,
John C.
Clayton,
Sally
Rawlins,
Amanda
Hellyer, and
Richard
Safford
Plant Sciences, Colworth House, Unilever Research and Development
Laboratory, Sharnbrook, Bedford MK44 1LQ, United Kingdom
The first committed step in the conversion of cycloartenol
into
5 C24-alkyl sterols in plants is catalyzed by an
S-adenosyl-methionine-dependent sterol-C24-methyltransferase type 1 (SMT1). We report the consequences of overexpressing SMT1 in tobacco (Nicotiana tabacum),
under control of either the constitutive carnation etched ring virus
promoter or the seed-specific Brassica napus
acyl-carrier protein promoter, on sterol biosynthesis in seed tissue.
Overexpression of SMT1 with either promoter increased the amount of
total sterols in seed tissue by up to 44%. The sterol composition was
also perturbed with levels of sitosterol increased by up to 50% and
levels of isofucosterol and campesterol increased by up to 80%,
whereas levels of cycloartenol and cholesterol were decreased by up to 53% and 34%, respectively. Concomitant with the enhanced SMT1 activity was an increase in endogenous 3-hydroxy-3-methylglutaryl coenzyme A reductase activity, from which one can speculate that reduced levels of cycloartenol feed back to up-regulate
3-hydroxy-3-methylglutaryl coenzyme A reductase activity and thereby
control the carbon flux into sterol biosynthesis. This potential
regulatory role of SMT1 in seed sterol biosynthesis is discussed.
*
Corresponding author; e-mail
niklas.holmberg{at}alligatorbio-science.com; fax 46-2864290.
© 2002 American Society of Plant Physiologists