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JXB Advance Access originally published online on December 12, 2003
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Journal of Experimental Botany, Vol. 55, No. 395, pp. 199-204, January 1, 2004
© 2004 Oxford University Press


Signalling in Abiotic Stress

The effects of manipulating phospholipase C on guard cell ABA-signalling

Received 12 May 2003; Accepted 8 October 2003

Lewis N. Mills1, Lee Hunt2, Calum P. Leckie3, Fiona L. Aitken2, Mark Wentworth2, Martin R. McAinsh1, Julie E. Gray2 and Alistair M. Hetherington1,*

1 Department of Biological Sciences, Lancaster Environment Centre, University of Lancaster, Lancaster LA1 4YQ, UK
2 Department of Molecular Biology and Biotechnology, University of Sheffield, Western Bank, Sheffield S10 2TN, UK
3 School of Cell and Molecular Biosciences, Medical School, University of Newcastle Upon Tyne, Framlington Place, Newcastle Upon Tyne NE2 4HH, UK

* To whom correspondence should be addressed. Fax: +44 (0)1524 843854. E-mail: A.Hetherington{at}lancaster.ac.uk

Studies using stably transformed tobacco plants containing very low levels of PI-PLC in their guard cells show that this enzyme plays a role in the events associated with the inhibition of stomatal opening by ABA, but not in the cellular reactions that are responsible for ABA-induced stomatal closure. However, Commelina communis guard cells microinjected with the InsP3 antagonist, heparin, fail to close on addition of ABA. There are three possible explanations for this apparent data mismatch. The differences may be indicative of species-specific signalling pathways, the presence of a PI-PLC isoform(s) that is not down-regulated in these transgenic lines and/or they may reflect differences between short-term (acute) administration of an inhibitor and long-term (chronic) effects of gene manipulation. It is possible that the guard cell is a robust signalling system that is able to adapt or compensate for the chronic loss of PI-PLC, but which is unable to adjust quickly to acute loss of this component. It would be interesting to investigate this possibility further using either transient manipulation of gene expression or through the use of an inducible promoter.

Key words: Abscisic acid, calcium ions, guard cell, phospholipase C, signalling, stomata.


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