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SIPK conditions transcriptional responses unique to either bacterial or oomycete elicitation in tobacco.

Authors :
HALL, HARDY C.
SAMUEL, MARCUS A.
ELLIS, BRIAN E.
Source :
Molecular Plant Pathology. Sep2007, Vol. 8 Issue 5, p581-594. 14p. 2 Color Photographs, 2 Charts, 2 Graphs.
Publication Year :
2007

Abstract

The mitogen-activated protein kinase, SIPK (salicylic acid-induced protein kinase), is known to be rapidly activated in tobacco ( Nicotiana tabacum) by various elicitors. However, SIPK activation induced by the oomycete elicitor, β-megaspermin, is reported to require external calcium influx, whereas that induced by the bacterial elicitor, hrpZPsph, does not. This suggests that SIPK activation is involved in different elicitor-initiated signalling pathways, and raises the question of whether the role(s) of SIPK in mediating stress outcomes, including transcriptional re-programming, differs in an elicitor-specific manner. To examine this, we compared the impact of silencing SIPK on the transcript profile of tobacco suspension culture cells challenged with either hrpZPsph or β-megaspermin. SIPK-silencing was found to have a substantial impact on both hrpZPsph- and β-megaspermin-induced transcriptional responses, and these impacts included both common and elicitor-differentiated features. As well as revealing a role for SIPK in modulating expression of known redox- and defence-related genes in response to both elicitors, our analysis detected a substantial impact of SIPK silencing on transcription of 80S ribosomal subunit mRNAs. This novel observation suggests that SIPK may play a role in affecting translation efficiency as one mechanism for enacting rapid genome-wide, elicitor-specific physiological reprogramming during defence responses. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14646722
Volume :
8
Issue :
5
Database :
Academic Search Index
Journal :
Molecular Plant Pathology
Publication Type :
Academic Journal
Accession number :
26279540
Full Text :
https://doi.org/10.1111/j.1364-3703.2007.00424.x