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JXB Advance Access originally published online on January 22, 2007
Journal of Experimental Botany 2007 58(5):1035-1045; doi:10.1093/jxb/erl266
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© 2007 The Author(s).
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.This paper is available online free of all access charges (see
http://jxb.oxfordjournals.org/open_access.html for further details)


RESEARCH PAPER

Co-ordinated gene expression during phases of dormancy release in raspberry (Rubus idaeus L.) buds

Luca Mazzitelli1, Robert D. Hancock1, Sophie Haupt1, Paul G. Walker1, Simon D. A. Pont1, Jim McNicol3, Linda Cardle2, Jenny Morris2, Roberto Viola1 *, Rex Brennan2, Peter E. Hedley2 and Mark A. Taylor1,{dagger}

1Quality, Health and Nutrition, Scottish Crop Research Institute, Invergowrie, Dundee DD2 5DA, UK
2Genetics Programme, Scottish Crop Research Institute, Invergowrie, Dundee DD2 5DA, UK
3Biomathematics and Statistics Scotland, Scottish Crop Research Institute, Invergowrie, Dundee DD2 5DA, UK

{dagger} To whom correspondence should be addressed. E-mail: mtaylo{at}scri.sari.ac.uk

Bud break in raspberry (Rubus idaeus L.) is often poor and uneven, with many of the subapical buds remaining in a dormant state. In order to determine the dormancy status of raspberry buds, an empirical measure of bud burst in a growth-permissive environment following exposure to chilling (4 °C cold storage) was developed. For cv. Glen Ample, percentage bud burst in intact canes and isolated nodes was recorded after 14 d. Isolated nodes (a measure of endodormancy) achieved 100% bud burst after ~1500 h chilling whereas buds on intact plants (combined endo- and paradormancy) required an additional 1000 h chilling. A microarray approach was used to follow changes in gene expression that occurred during dormancy transition. The probes for the microarrays were obtained from endodormant and paradormant raspberry bud cDNA libraries. The expression profiles of 5300 clones from these libraries were subjected to principal component analysis to determine the most significant expression patterns. Sequence analysis of these clones, in many cases, enabled their functional categorization and the development of hypotheses concerning the mechanisms of bud dormancy release. Thus a set of novel candidates for key dormancy-related genes from raspberry buds have been identified. Bud dormancy is fundamental to the study of plant developmental processes and, in addition, its regulation is of significant economic importance to fruit and horticultural industries.

Key words: Dormancy, forcing, gene expression, microarray, raspberry buds


* Present address: IASMA, Via E. Mach, S. Michele all'Adige, I38010 [GenBank] , I-Trento, Italy.

Received 31 August 2006; Revised 8 November 2006 Accepted 9 November 2006


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