Transgenic Arabidopsis plants expressing a fungal cutinase show alterations in the structure and properties of the cuticle and postgenital organ fusions.
Details
Serval ID
serval:BIB_23FEFFDCFD88
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Transgenic Arabidopsis plants expressing a fungal cutinase show alterations in the structure and properties of the cuticle and postgenital organ fusions.
Journal
Plant Cell
ISSN
1040-4651 (Print)
ISSN-L
1040-4651
Publication state
Published
Issued date
2000
Volume
12
Number
5
Pages
721-738
Language
english
Abstract
A major structural component of the cuticle of plants is cutin. Analysis of the function of cutin in vivo has been limited because no mutants with specific defects in cutin have been characterized. Therefore, transgenic Arabidopsis plants were generated that express and secrete a cutinase from Fusarium solani f sp pisi. Arabidopsis plants expressing the cutinase in the extracellular space showed an altered ultrastructure of the cuticle and an enhanced permeability of the cuticle to solutes. In addition, pollen could germinate on fully differentiated leaves of cutinase-expressing plants but not on control leaves. These differences coincided with strong postgenital organ fusions. The junctions of the fusions contained pectic polysaccharides. As fused organs grew apart from each other, organ deformations and protrusions of epidermal cells developed at positions with high mechanical stress. These results demonstrate that an intact cutin layer not only is important for plant-environment interactions but also prevents fusions between different plant organs and is therefore necessary for normal epidermal differentiation and organ formation.
Keywords
Arabidopsis/anatomy & histology, Arabidopsis/genetics, Base Sequence, Carboxylic Ester Hydrolases/genetics, DNA Primers, Fusarium/enzymology, Microscopy, Electron, Scanning, Plants, Genetically Modified/anatomy & histology, Plants, Genetically Modified/genetics
Pubmed
Web of science
Open Access
Yes
Create date
24/01/2008 19:49
Last modification date
20/08/2019 13:01