Simpson Craig G, Fuller John, Maronova Monika, Kalyna Maria, Davidson Diane, McNicol Jim, Barta Andrea, Brown John W S
Genetics Programme, SCRI, Invergowrie, Dundee DD2 5DA, UK.
Plant J. 2008 Mar;53(6):1035-48. doi: 10.1111/j.1365-313X.2007.03392.x. Epub 2007 Dec 15.
Alternative splicing (AS) increases the proteomic and functional capacity of genomes through the generation of alternative mRNA transcripts from the same gene. AS is now estimated to occur in a third of Arabidopsis and rice genes, and includes genes involved in the control of growth and development, responses to stress and signalling. Regulation of AS reflects the interactions between positive and negative cis sequences in the precursor messenger RNA and a range of trans-acting factors. The levels and activities of these factors differ in different cells and growth conditions. To identify changes in AS in multiple genes simultaneously, we have established a reproducible RT-PCR panel that can analyse 96 alternative splicing events and accurately measure the ratio of alternatively spliced products. This procedure detected statistically significant changes in AS in different plant organs, in plants grown under different light and day-length conditions, and in plants overexpressing splicing factors. The system provides a convenient, medium-throughput means of monitoring changes in AS in multiple genes. It can readily be applied to much larger or targeted sets of gene transcripts to generate information on the significance and regulation of AS in plant growth and development, specific processes and responses to external stimuli.
可变剪接(AS)通过从同一基因产生可变的mRNA转录本,增加了基因组的蛋白质组和功能容量。目前估计,拟南芥和水稻中三分之一的基因会发生可变剪接,其中包括参与生长发育调控、应激反应和信号传导的基因。可变剪接的调控反映了前体信使RNA中正向和负向顺式序列与一系列反式作用因子之间的相互作用。这些因子的水平和活性在不同细胞和生长条件下有所不同。为了同时鉴定多个基因中可变剪接的变化,我们建立了一个可重复的RT-PCR检测板,该检测板可以分析96个可变剪接事件,并准确测量可变剪接产物的比例。该方法检测到了不同植物器官、在不同光照和日长条件下生长的植物以及过表达剪接因子的植物中可变剪接的统计学显著变化。该系统提供了一种方便的、中等通量的方法来监测多个基因中可变剪接的变化。它可以很容易地应用于更大或有针对性的基因转录本组,以生成关于可变剪接在植物生长发育、特定过程以及对外部刺激反应中的意义和调控的信息。