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Originally published In Press as doi:10.1074/jbc.C100152200 on April 19, 2001

J. Biol. Chem., Vol. 276, Issue 24, 20817-20820, June 15, 2001
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ACCELERATED PUBLICATION
A New Pathway for Heavy Metal Detoxification in Animals
PHYTOCHELATIN SYNTHASE IS REQUIRED FOR CADMIUM TOLERANCE IN CAENORHABDITIS ELEGANS*

Olena K. VatamaniukDagger §, Elizabeth A. BucherDagger , James T. Ward, and Philip A. Rea§||

From the § Department of Biology, Plant Science Institute, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6018 and the  Department of Cell and Developmental Biology, School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6058

Increasing emissions of heavy metals such as cadmium, mercury, and arsenic into the environment pose an acute problem for all organisms. Considerations of the biochemical basis of heavy metal detoxification in animals have focused exclusively on two classes of peptides, the thiol tripeptide, glutathione (GSH, gamma -Glu-Cys-Gly), and a diverse family of cysteine-rich low molecular weight proteins, the metallothioneins. Plants and some fungi, however, not only deploy GSH and metallothioneins for metal detoxification but also synthesize another class of heavy metal binding peptides termed phytochelatins (PCs) from GSH. Here we show that PC-mediated heavy metal detoxification is not restricted to plants and some fungi but extends to animals by demonstrating that the ce-pcs-1 gene of the nematode worm Caenorhabditis elegans encodes a functional PC synthase whose activity is critical for heavy metal tolerance in the intact organism.


* This work was supported in part by National Science Foundation Grant MCB-0077838 (to P. A. R.) and National Institutes of Health Grant RO1-HL 59680-0 (to E. A. B.). O. K. V. was sponsored by PlantGenix, Inc., Philadelphia, PA.The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

The nucleotide sequence(s) reported in this paper has been submitted to the GenBankTM/EMBL Data Bank with accession number(s) AF29932 and AF29933.

Dagger Contributed equally to this work.

|| To whom correspondence should be addressed. Tel.: 215-898-0807; Fax: 215-898-8780; E-mail: parea@sas.upenn.edu.


Copyright © 2001 by The American Society for Biochemistry and Molecular Biology, Inc.
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