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Plant Physiol, January 2000, Vol. 122, pp. 85-98

A Putative Role for the Tomato Genes DUMPY and CURL-3 in Brassinosteroid Biosynthesis and Response1

Chala V. Koka,2 R. Eric Cerny,23 Randy G. Gardner, Takahiro Noguchi, Shozo Fujioka, Suguru Takatsuto, Shigeo Yoshida, and Steven D. Clouse*

Department of Horticultural Science, Box 7609, North Carolina State University, Raleigh, North Carolina 27695 (C.V.K., R.E.C., S.D.C.); Mountain Horticultural Crops Research and Extension Center, North Carolina State University, Fletcher, North Carolina 28732 (R.G.G.); The Institute of Physical and Chemical Research (RIKEN), Wako-shi, Saitama 351-0198, Japan (T.N., S.F., S.Y.); and Department of Chemistry, Joetsu University of Education, Joetsu-shi, Niigata 943-8512, Japan (S.T.).

The dumpy (dpy) mutant of tomato (Lycopersicon esculentum Mill.) exhibits short stature, reduced axillary branching, and altered leaf morphology. Application of brassinolide and castasterone rescued the dpy phenotype, as did C-23-hydroxylated, 6-deoxo intermediates of brassinolide biosynthesis. The brassinolide precursors campesterol, campestanol, and 6-deoxocathasterone failed to rescue, suggesting that dpy may be affected in the conversion of 6-deoxocathasterone to 6-deoxoteasterone, similar to the Arabidopsis constitutive photomorphogenesis and dwarfism (cpd) mutant. Measurements of endogenous brassinosteroid levels by gas chromatography-mass spectrometry were consistent with this hypothesis. To examine brassinosteroid-regulated gene expression in dpy, we performed cDNA subtractive hybridization and isolated a novel xyloglucan endotransglycosylase that is regulated by brassinosteroid treatment. The curl-3 (cu-3) mutant (Lycopersicon pimpinellifolium [Jusl.] Mill.) shows extreme dwarfism, altered leaf morphology, de-etiolation, and reduced fertility, all strikingly similar to the Arabidopsis mutant brassinosteroid insensitive 1 (bri1). Primary root elongation of wild-type L. pimpinellifolium seedlings was strongly inhibited by brassinosteroid application, while cu-3 mutant roots were able to elongate at the same brassinosteroid concentration. Moreover, cu-3 mutants retained sensitivity to indole-3-acetic acid, cytokinins, gibberellin, and abscisic acid while showing hypersensitivity to 2,4-dichlorophenoxyacetic acid in the root elongation assay. The cu-3 root response to hormones, coupled with its bri1-like phenotype, suggests that cu-3 may also be brassinosteroid insensitive.


1 This work was supported by the North Carolina Agricultural Research Service and the U.S. Department of Agriculture National Research Initiative Competitive Grants Program.

2 These authors contributed equally to the paper.

3 Present address: AA2G, Plant Growth and Development Group, Monsanto Co., 700 Chesterfield Parkway North, St. Louis, MO 63198.

* Corresponding author; e-mail steve_clouse{at}ncsu.edu; fax 919-515-2505.

© 2000 American Society of Plant Physiologists



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