Pawłowski Tomasz A
Seed Biochemistry Laboratory, Institute of Dendrology Polish Academy of Sciences, Kórnik, Poland.
BMC Plant Biol. 2009 May 4;9:48. doi: 10.1186/1471-2229-9-48.
Seed dormancy is controlled by the physiological or structural properties of a seed and the external conditions. It is induced as part of the genetic program of seed development and maturation. Seeds with deep physiological embryo dormancy can be stimulated to germinate by a variety of treatments including cold stratification. Hormonal imbalance between germination inhibitors (e.g. abscisic acid) and growth promoters (e.g. gibberellins) is the main cause of seed dormancy breaking. Differences in the status of hormones would affect expression of genes required for germination. Proteomics offers the opportunity to examine simultaneous changes and to classify temporal patterns of protein accumulation occurring during seed dormancy breaking and germination. Analysis of the functions of the identified proteins and the related metabolic pathways, in conjunction with the plant hormones implicated in seed dormancy breaking, would expand our knowledge about this process.
A proteomic approach was used to analyse the mechanism of dormancy breaking in Norway maple seeds caused by cold stratification, and the participation of the abscisic (ABA) and gibberellic (GA) acids. Forty-four proteins showing significant changes were identified by mass spectrometry. Of these, eight spots were identified as water-responsive, 18 spots were ABA- and nine GA-responsive and nine spots were regulated by both hormones. The classification of proteins showed that most of the proteins associated with dormancy breaking in water were involved in protein destination. Most of the ABA- and GA-responsive proteins were involved in protein destination and energy metabolism.
In this study, ABA was found to mostly down-regulate proteins whereas GA up-regulated proteins abundance. Most of the changes were observed at the end of stratification in the germinated seeds. This is the most active period of dormancy breaking when seeds pass from the quiescent state to germination. Seed dormancy breaking involves proteins of various processes but the proteasome proteins, S-adenosylmethionine synthetase, glycine-rich RNA binding protein, ABI3-interacting protein 1, EF-2 and adenosylhomocysteinase are of particular importance. The effect of exogenously applied hormones was not a determining factor for total inhibition (ABA) or stimulation (GA) of Norway maple seed dormancy breaking and germination but proteomic data has proven these hormones play a role.
种子休眠受种子的生理或结构特性以及外部条件控制。它是种子发育和成熟遗传程序的一部分。具有深度生理胚休眠的种子可通过包括冷层积在内的多种处理刺激发芽。发芽抑制剂(如脱落酸)和生长促进剂(如赤霉素)之间的激素失衡是种子休眠打破的主要原因。激素状态的差异会影响发芽所需基因的表达。蛋白质组学为研究种子休眠打破和发芽过程中同时发生的变化以及对蛋白质积累的时间模式进行分类提供了机会。分析已鉴定蛋白质的功能和相关代谢途径,结合与种子休眠打破相关的植物激素,将扩展我们对这一过程的认识。
采用蛋白质组学方法分析冷层积导致挪威槭种子休眠打破的机制以及脱落酸(ABA)和赤霉素(GA)的参与情况。通过质谱鉴定出44种显示出显著变化的蛋白质。其中,8个斑点被鉴定为对水有反应,18个斑点对ABA有反应,9个斑点对GA有反应,9个斑点受两种激素调节。蛋白质分类显示,大多数与在水中休眠打破相关的蛋白质参与蛋白质转运。大多数对ABA和GA有反应的蛋白质参与蛋白质转运和能量代谢。
在本研究中,发现ABA主要下调蛋白质,而GA上调蛋白质丰度。大多数变化在层积结束时的发芽种子中观察到。这是休眠打破最活跃的时期,此时种子从静止状态进入发芽状态。种子休眠打破涉及各种过程的蛋白质,但蛋白酶体蛋白质、S-腺苷甲硫氨酸合成酶、富含甘氨酸的RNA结合蛋白、ABI3相互作用蛋白1、EF-2和腺苷同型半胱氨酸酶尤为重要。外源施用激素的效果不是挪威槭种子休眠打破和发芽完全抑制(ABA)或刺激(GA)的决定因素,但蛋白质组学数据已证明这些激素发挥了作用。