Heintz Dimitri, Erxleben Anika, High Anthony A, Wurtz Virginie, Reski Ralf, Van Dorsselaer Alain, Sarnighausen Eric
Laboratoire de Spectrométrie de Masse Bio-Organique, CNRS, ECPM, Université Louis Pasteur, 25 rue Becquerel F67087, Strasbourg, Cedex 2, France.
J Proteome Res. 2006 Sep;5(9):2283-93. doi: 10.1021/pr060152e.
Cytokinin hormones are crucial regulators of a large number of processes in plant development. Recently, significant progress has been made toward the elucidation of the molecular details of cytokinin that has led to a model for signal transduction involving a phosphorylation cascade. However, the current knowledge of cytokinin action remains largely unknown and does not explain the different roles of this hormone. To gain further insights into this aspect of cytokinin action and the inducible phosphorelay, we have produced the first large-scale map of a phosphoproteome in the moss Physcomitrella patens. Using a protocol that we recently published (Heintz, D.; et al. Electrophoresis 2004, 25, 1149-1159) that combines IMAC, MALDI-TOF-MS, and LC-MS/MS, a total of 172 phosphopeptide sequences were obtained by a peptide de novo sequencing strategy. Specific P. patens EST and raw genomic databases were interrogated, and protein homology searches resulted in the identification of 112 proteins that were then classified into functional categories. In addition, the temporal dynamics of the phosphoproteome in response to cytokinin stimulation was studied at 2, 4, 6, and 15 min after hormone addition. We identified 13 proteins that were not previously known targets of cytokinin action. Among the responsive proteins, some were involved in metabolism, and several proteins of unknown function were also identified. We have mapped the time course of their activation in response to cytokinin and discussed their hypothetical biological significance. Deciphering these early induced phosphorylation events has shown that the cytokinin effect can be rapid (few minutes), and the duration of this effect can be variable. Also phosphorylation events can be differentially regulated. Taken together our proteomic study provides an enriched look of the multistep phosphorelay system mediating cytokinin response and suggests the existence of a multidirectional interaction between cytokinin and numerous other pathways.
细胞分裂素类激素是植物发育过程中大量生理过程的关键调节因子。最近,在阐明细胞分裂素分子细节方面取得了重大进展,这促成了一个涉及磷酸化级联反应的信号转导模型。然而,目前关于细胞分裂素作用的知识仍大多未知,无法解释这种激素的不同作用。为了进一步深入了解细胞分裂素作用的这一方面以及诱导型磷酸化信号转导,我们绘制了首个苔藓植物小立碗藓磷酸化蛋白质组的大规模图谱。使用我们最近发表的一种方法(海因茨,D.等人,《电泳》2004年,25卷,1149 - 1159页),该方法结合了固定化金属离子亲和色谱(IMAC)、基质辅助激光解吸电离飞行时间质谱(MALDI - TOF - MS)和液相色谱 - 串联质谱(LC - MS/MS),通过肽从头测序策略总共获得了172个磷酸肽序列。对特定的小立碗藓EST和原始基因组数据库进行了查询,并通过蛋白质同源性搜索鉴定出112种蛋白质,然后将其分类到功能类别中。此外,在添加激素后的2、4、6和15分钟研究了磷酸化蛋白质组对细胞分裂素刺激的时间动态变化。我们鉴定出13种以前未知的细胞分裂素作用靶点的蛋白质。在响应蛋白中,一些参与代谢,还鉴定出了几种功能未知的蛋白质。我们绘制了它们响应细胞分裂素激活的时间进程,并讨论了它们可能的生物学意义。对这些早期诱导的磷酸化事件的解析表明,细胞分裂素的作用可以很快(几分钟),而且这种作用的持续时间可能不同。此外,磷酸化事件可以受到不同的调节。综合来看,我们的蛋白质组学研究提供了对介导细胞分裂素响应的多步骤磷酸化信号转导系统更丰富的认识,并表明细胞分裂素与众多其他信号通路之间存在多向相互作用。