Mazzitelli Luca, Hancock Robert D, Haupt Sophie, Walker Paul G, Pont Simon D A, McNicol Jim, Cardle Linda, Morris Jenny, Viola Roberto, Brennan Rex, Hedley Peter E, Taylor Mark A
Quality, Health and Nutrition, Scottish Crop Research Institute, Invergowrie, Dundee DD2 5DA, UK.
J Exp Bot. 2007;58(5):1035-45. doi: 10.1093/jxb/erl266. Epub 2007 Jan 22.
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 degrees 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 approximately 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.
树莓(悬钩子属)的芽萌发往往较差且不均匀,许多亚顶端芽仍处于休眠状态。为了确定树莓芽的休眠状态,开发了一种经验方法,即测量在经历低温处理(4℃冷藏)后,在允许生长的环境中芽的萌发情况。对于“格伦安普尔”品种,在14天后记录完整茎和离体节段的芽萌发率。离体节段(一种内休眠的测量方法)在大约1500小时的低温处理后达到100%的芽萌发率,而完整植株上的芽(内休眠和外休眠共同作用)则需要额外1000小时的低温处理。采用微阵列方法跟踪休眠转变过程中发生的基因表达变化。微阵列的探针取自内休眠和外休眠的树莓芽cDNA文库。对来自这些文库的5300个克隆的表达谱进行主成分分析,以确定最显著的表达模式。在许多情况下,对这些克隆进行序列分析能够对其进行功能分类,并提出关于芽休眠解除机制的假设。因此,已鉴定出一组来自树莓芽的与休眠相关的关键基因的新候选基因。芽休眠是植物发育过程研究的基础,此外,其调控对水果和园艺产业具有重要的经济意义。