First published online April 10, 2003; 10.1104/pp.102.012633
Plant Physiol, May 2003, Vol. 132, pp. 343-351
The Expression of the t-SNARE AtSNAP33 Is Induced by Pathogens
and Mechanical Stimulation1
Peter
Wick,23
Xavier
Gansel,24
Catherine
Oulevey,
Valérie
Page,5
Ingrid
Studer,
Michael
Dürst, and
Liliane
Sticher*
Department of Biology, Plant Biology Unit, University of Fribourg,
CH-1700 Fribourg, Switzerland
The fusion of vesicles in the secretory pathway involves the
interaction of t-soluble N-ethylmaleimide-sensitive
factor attachment protein receptors (t-SNAREs) on the target membrane
and v-SNAREs on the vesicle membrane. AtSNAP33 is an Arabidopsis
homolog of the neuronal t-SNARE SNAP-25 involved in exocytosis and is
localized at the cell plate and at the plasma membrane. In this paper,
the expression of AtSNAP33 was analyzed after different
biotic and abiotic stresses. The expression of AtSNAP33
increased after inoculation with the pathogens Plectosporium
tabacinum and virulent and avirulent forms of
Peronospora parasitica and Pseudomonas
syringae pv tomato. The expression of
PR1 transcripts encoding the secreted
pathogenesis-related protein 1 also increased after inoculation with
these pathogens and the expression of AtSNAP33 preceded
or occurred at the same time as the expression of PR1.
AtSNAP33 was also expressed in npr1 plants that
do not express PR1 after pathogen inoculation as well as in
cpr1 plants that overexpress PR1 in the absence of a
pathogen. The level of AtSNAP33 decreased slightly in
leaves inoculated with P. parasitica in the
NahG plants, and eds5 and sid2 mutants that are unable to accumulate salicylic
acid (SA) after pathogen inoculation, indicating a partial dependence
on SA. AtSNAP33 was also expressed in systemic
noninoculated leaves of plants inoculated with P.
syringae. In contrast to the situation in infected leaves, the
expression of AtSNAP33 in systemic leaves was fully SA
dependent. Thus, the expression of AtSNAP33 after pathogen attack is regulated by SA-dependent and SA-independent pathways. Mechanical stimulation also led to an increase of
AtSNAP33 transcripts.
1
This work was supported by the Swiss National
Foundation for Scientific Research (grant no. 31-39595.93 to
L.S.).
2
These authors contributed equally to this paper.
3
Present address: EMPA, Lerchenfeld 5, 9014 St-Gallen, Switzerland.
4
Present address: Biomerieux, Parc du Moulin à
Vent, Av. du Docteur Levy 33, 69693 Vernissieux cedex, France.
5
Present address: Institute of Plant Sciences, University
of Bern, Altenbergrain 21, 3013 Bern, Switzerland.
*
Corresponding author; e-mail Liliane.Sticher{at}unifr.ch; fax
41-26-300-97-40.
© 2003 American Society of Plant Biologists
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