Author
Listed:
- Kevin L.-C. Wang
(The Salk Institute for Biological Studies
University of Pennsylvania)
- Hitoshi Yoshida
(University of Pennsylvania
National Agricultural Research Center
INRA-URGV)
- Claire Lurin
(University of Pennsylvania
National Agricultural Research Center
INRA-URGV)
- Joseph R. Ecker
(The Salk Institute for Biological Studies
University of Pennsylvania)
Abstract
Ethylene gas is used as a hormone by plants, in which it acts as a critical growth regulator. Its synthesis is also rapidly evoked in response to a variety of biotic and abiotic stresses1,2. The Arabidopsis ethylene-overproducer mutants eto2 and eto3 have previously been identified as having mutations in two genes, ACS5 and ACS9, respectively; these encode isozymes of 1-aminocyclopropane-1-carboxylic acid synthase (ACS), which catalyse the rate-limiting step in ethylene biosynthesis3,4. Here we report that another ethylene-overproducer mutation, eto1, is in a gene that negatively regulates ACS activity and ethylene production. The ETO1 protein directly interacts with and inhibits the enzyme activity of full-length ACS5 but not of a truncated form of the enzyme, resulting in a marked accumulation of ACS5 protein and ethylene. Overexpression of ETO1 inhibited induction of ethylene production by the plant growth regulator cytokinin, and promoted ACS5 degradation by a proteasome-dependent pathway. ETO1 also interacts with CUL3, a constituent of ubiquitin ligase complexes in which we propose that ETO1 serves as a substrate-specific adaptor protein. ETO1 thus has a dual mechanism, inhibiting ACS enzyme activity and targeting it for protein degradation. This permits rapid modulation of the concentration of ethylene.
Suggested Citation
Kevin L.-C. Wang & Hitoshi Yoshida & Claire Lurin & Joseph R. Ecker, 2004.
"Regulation of ethylene gas biosynthesis by the Arabidopsis ETO1 protein,"
Nature, Nature, vol. 428(6986), pages 945-950, April.
Handle:
RePEc:nat:nature:v:428:y:2004:i:6986:d:10.1038_nature02516
DOI: 10.1038/nature02516
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