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First published online June 11, 2004; 10.1104/pp.104.040113

Plant Physiology 135:840-848 (2004)
© 2004 American Society of Plant Biologists

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BIOCHEMICAL PROCESSES AND MACROMOLECULAR STRUCTURES

Functional Analysis of the Tandem-Duplicated P450 Genes SPS/BUS/CYP79F1 and CYP79F2 in Glucosinolate Biosynthesis and Plant Development by Ds Transposition-Generated Double Mutants1

Titima Tantikanjana2, Michael Dalgaard Mikkelsen, Mumtaz Hussain, Barbara Ann Halkier and Venkatesan Sundaresan*

Department of Plant Biology and Agronomy, University of California, Davis, California 95616 (T.T., V.S.); Plant Biochemistry Laboratory, Department of Plant Biology, The Royal Veterinary and Agricultural University, DK–1871 Frederiksberg C, Denmark (M.D.M., B.A.H.); and Institute of Molecular and Cell Biology, Singapore 11760 (M.H.)

A significant fraction (approximately 17%) of Arabidopsis genes are members of tandemly repeated families and pose a particular challenge for functional studies. We have used the Ac-Ds transposition system to generate single- and double-knockout mutants of two tandemly duplicated cytochrome P450 genes, SPS/BUS/CYP79F1 and CYP79F2. We have previously described the Arabidopsis supershoot mutants in CYP79F1 that exhibit massive overproliferation of shoots. Here we use a cytokinin-responsive reporter ARR5::uidA and an auxin-responsive reporter DR5::uidA in the sps/cyp79F1 mutant to show that increased levels of cytokinin, but not auxin, correlate well with the expression pattern of the SPS/CYP79F1 gene, supporting the involvement of this gene in cytokinin homeostasis. Further, we isolated Ds gene trap insertions in the CYP79F2 gene, and find these mutants to be defective mainly in the root system, consistent with a root-specific expression pattern. Finally, we generated double mutants in CYP79F1 and CYP79F2 using secondary transpositions, and demonstrate that the phenotypes are additive. Previous biochemical studies have suggested partially redundant functions for SPS/CYP79F1 and CYP79F2 in aliphatic glucosinolate synthesis. Our analysis shows that aliphatic glucosinolate biosynthesis is completely abolished in the double-knockout plants, providing genetic proof for the proposed biochemical functions of these genes. This study also provides further demonstration of how gluconisolate biosynthesis, regarded as secondary metabolism, is intricately linked with hormone homeostatis and hence with plant growth and development.


1 This work was supported by the National Science Foundation, the Danish National Research Foundation, and the University of California, Davis.

2 Present address: Department of Plant Biology, Cornell University, Ithaca, NY 14853.

Article, publication date, and citation information can be found at www.plantphysiol.org/cgi/doi/10.1104/pp.104.040113.

* Corresponding author; e-mail sundar{at}ucdavis.edu; fax 530–752–5410.

Received January 31, 2004; returned for revision March 29, 2004; accepted March 30, 2004.




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