Recessive and dominant mutations in the ethylene biosynthetic gene ACS5 of Arabidopsis confer cytokinin insensitivity and ethylene overproduction, respectively

We identified a set of cytokinin-insensitive mutants by using a screen based on the ethylene-mediated triple response observed after treatment with low levels of cytokinins. One group of these mutants disrupts ACS5, a member of the Arabidopsis gene family that encodes 1-amino-cyclopropane-1-carboxyl...

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Published inProceedings of the National Academy of Sciences - PNAS Vol. 95; no. 8; pp. 4766 - 4771
Main Authors Vogel, J.P. (Carnegie Institution of Washington, Stanford, CA.), Woeste, K.E, Theologis, A, Kieber, J.J
Format Journal Article
LanguageEnglish
Published United States National Academy of Sciences of the United States of America 14.04.1998
National Acad Sciences
National Academy of Sciences
The National Academy of Sciences
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Summary:We identified a set of cytokinin-insensitive mutants by using a screen based on the ethylene-mediated triple response observed after treatment with low levels of cytokinins. One group of these mutants disrupts ACS5, a member of the Arabidopsis gene family that encodes 1-amino-cyclopropane-1-carboxylate synthase, the first enzyme in ethylene biosynthesis. The ACS5 isoform is mainly responsible for the sustained rise in ethylene biosynthesis observed in response to low levels of cytokinin and appears to be regulated primarily by a posttranscriptional mechanism. Furthermore, the dominant ethylene-overproducing mutant eto2 was found to be the result of an alteration of the carboxy terminus of ACS5, suggesting that this domain acts as a negative regulator of ACS5 function
Bibliography:1997092014
F30
To whom reprint requests should be addressed at: University of Illinois, Molecular Biology Research Facility, Laboratory for Molecular Biology (M/C 567), 900 South Ashland Avenue, Chicago, IL 60607. e-mail: jkieber@uic.edu.
Present address: Carnegie Institution of Washington, Department of Plant Biology, Stanford, CA 94305.
Edited by Hans J. Kende, Michigan State University, East Lansing, MI, and approved January 27, 1998
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.95.8.4766