The SHINE clade of AP2 domain transcription factors activates wax biosynthesis, alters cuticle properties, and confers drought tolerance when overexpressed in Arabidopsis.
Journal: 2004/December - Plant Cell
ISSN: 1040-4651
Abstract:
The interface between plants and the environment plays a dual role as a protective barrier as well as a medium for the exchange of gases, water, and nutrients. The primary aerial plant surfaces are covered by a cuticle, acting as the essential permeability barrier toward the atmosphere. It is a heterogeneous layer composed mainly of lipids, namely cutin and intracuticular wax with epicuticular waxes deposited on the surface. We identified an Arabidopsis thaliana activation tag gain-of-function mutant shine (shn) that displayed a brilliant, shiny green leaf surface with increased cuticular wax compared with the leaves of wild-type plants. The gene responsible for the phenotype encodes one member of a clade of three proteins of undisclosed function, belonging to the plant-specific family of AP2/EREBP transcription factors. Overexpression of all three SHN clade genes conferred a phenotype similar to that of the original shn mutant. Biochemically, such plants were altered in wax composition (very long fatty acid derivatives). Total cuticular wax levels were increased sixfold in shn compared with the wild type, mainly because of a ninefold increase in alkanes that comprised approximately half of the total waxes in the mutant. Chlorophyll leaching assays and fresh weight loss experiments indicated that overexpression of the SHN genes increased cuticle permeability, probably because of changes in its ultrastructure. Likewise, SHN gene overexpression altered leaf and petal epidermal cell structure, trichome number, and branching as well as the stomatal index. Interestingly, SHN overexpressors displayed significant drought tolerance and recovery, probably related to the reduced stomatal density. Expression analysis using promoter-beta-glucuronidase fusions of the SHN genes provides evidence for the role of the SHN clade in plant protective layers, such as those formed during abscission, dehiscence, wounding, tissue strengthening, and the cuticle. We propose that these diverse functions are mediated by regulating metabolism of lipid and/or cell wall components.
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Plant Cell 16(9): 2463-2480

The SHINE Clade of AP2 Domain Transcription Factors Activates Wax Biosynthesis, Alters Cuticle Properties, and Confers Drought Tolerance when Overexpressed in Arabidopsis<sup><a href="#fn1" rid="fn1" class=" fn">W⃞</a></sup>

Plant Research International, 6700 AA, Wageningen, The Netherlands
Departments of Botany and Chemistry, University of British Columbia, Vancouver, British Columbia, Canada V6T 1Z4
To whom correspondence should be addressed. E-mail ln.ruw@arierep.ydna; fax 31-0317-418034.
Received 2004 Mar 24; Accepted 2004 May 11.

Abstract

The interface between plants and the environment plays a dual role as a protective barrier as well as a medium for the exchange of gases, water, and nutrients. The primary aerial plant surfaces are covered by a cuticle, acting as the essential permeability barrier toward the atmosphere. It is a heterogeneous layer composed mainly of lipids, namely cutin and intracuticular wax with epicuticular waxes deposited on the surface. We identified an Arabidopsis thaliana activation tag gain-of-function mutant shine (shn) that displayed a brilliant, shiny green leaf surface with increased cuticular wax compared with the leaves of wild-type plants. The gene responsible for the phenotype encodes one member of a clade of three proteins of undisclosed function, belonging to the plant-specific family of AP2/EREBP transcription factors. Overexpression of all three SHN clade genes conferred a phenotype similar to that of the original shn mutant. Biochemically, such plants were altered in wax composition (very long fatty acid derivatives). Total cuticular wax levels were increased sixfold in shn compared with the wild type, mainly because of a ninefold increase in alkanes that comprised approximately half of the total waxes in the mutant. Chlorophyll leaching assays and fresh weight loss experiments indicated that overexpression of the SHN genes increased cuticle permeability, probably because of changes in its ultrastructure. Likewise, SHN gene overexpression altered leaf and petal epidermal cell structure, trichome number, and branching as well as the stomatal index. Interestingly, SHN overexpressors displayed significant drought tolerance and recovery, probably related to the reduced stomatal density. Expression analysis using promoter-β-glucuronidase fusions of the SHN genes provides evidence for the role of the SHN clade in plant protective layers, such as those formed during abscission, dehiscence, wounding, tissue strengthening, and the cuticle. We propose that these diverse functions are mediated by regulating metabolism of lipid and/or cell wall components.

Abstract

The coverage of total extracted lipids and of individual compound classes are given as mean values with standard deviation. tr, traces (<0.05 μg/cm detectable). Level of significance obtained with a Student's t test are marked by the following: **, P < 0.05; ***, P < 0.01.

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Acknowledgments

We thank Nayelli Marsch-Martinez, Raffaella Greco, and Aarti Karaba for helpful discussions, Stephan Knapek, Stefanie Full, Sherry Wu, Charistian Landmann, and Markus Griezer along with Wim Dirkse, John Franken, and Stefan de-Folter for technical assistance, and Adrian van-Elst for assistance with scanning electron microscopy analysis. We gratefully acknowledge the use of the construct rd29A-DREB1A from Kazuo Shinozaki. This work was supported by the Center for Biosystems Genomics, Wageningen, The Netherlands.

Acknowledgments

Notes

The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantcell.org) is: Andy Pereira (ln.ruw@arierep.ydna).

Online version contains Web-only data.

Article, publication date, and citation information can be found at www.plantcell.org/cgi/doi/10.1105/tpc.104.022897.

Notes
The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantcell.org) is: Andy Pereira (ln.ruw@arierep.ydna).Article, publication date, and citation information can be found at www.plantcell.org/cgi/doi/10.1105/tpc.104.022897.

NOTE ADDED IN PROOF

  • Another similar study was recently published in PNAS.
  • Broun, P., Poindexter, P., Osborne, E., Jiang, C., and Riechmann, J.L. (2004). WIN1, a transcriptional activator of epidermal wax accumulation in Arabidopsis. Proc. Natl. Acad. Sci. USA101, 4706–4711. [PMC free article] [PubMed] [Google Scholar]
NOTE ADDED IN PROOF
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