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J. Biol. Chem., Vol. 276, Issue 24, 20817-20820, June 15, 2001
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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,
The nucleotide sequence(s) reported in this paper has been submitted to the GenBankTM/EMBL Data Bank with accession number(s) AF29932 and AF29933.
ACCELERATED PUBLICATION
A New Pathway for Heavy Metal Detoxification in Animals
PHYTOCHELATIN SYNTHASE IS REQUIRED FOR CADMIUM TOLERANCE IN
CAENORHABDITIS ELEGANS*
§,
¶,
-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.
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.
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