College of Agronomy, Northwest A&F University, Yangling 712100, China.
BMC Genomics. 2014 Jun 12;15(1):466. doi: 10.1186/1471-2164-15-466.
The cotton (Gossypium spp.) fiber cell is an important unicellular model for studying cell differentiation. There is evidence suggesting that phosphorylation is a critical post-translational modification involved in regulation of a wide range of cell activities. Nevertheless, the sites of phosphorylation in G. hirsutum and their regulatory roles in fiber cell initiation are largely unknown. In this study, we employed a mass spectrometry-based phosphoproteomics to conduct a global and site-specific phosphoproteome profiling between ovules of a fuzzless-lintless (fl) Upland cotton (G. hirsutum) mutant and its isogenic parental wild type (WT) at -3 and 0 days post-anthesis (DPA).
A total of 830 phosphopeptides and 1,592 phosphorylation sites from 619 phosphoproteins were identified by iTRAQ (isobaric tags for relative and absolute quantitation). Of these, 76 phosphoproteins and 1,100 phosphorylation sites were identified for the first time after searching the P3DB public database using the BLAST program. Among the detected phosphopeptides, 69 were differentially expressed between the fl mutant and its WT in ovules at -3 and 0 DPA. An analysis using the Motif-X program uncovered 19 phosphorylation motifs, 8 of which were unique to cotton. A further metabolic pathway analysis revealed that the differentially phosphorylated proteins were involved in signal transduction, protein modification, carbohydrate metabolic processes, and cell cycle and cell proliferation.
Our phosphoproteomics-based research provides the first global overview of phosphorylation during cotton fiber initiation, and also offers a helpful dataset for elucidation of signaling networks in fiber development of G. hirsutum.
棉花(Gossypium spp.)纤维细胞是研究细胞分化的重要单细胞模型。有证据表明,磷酸化是一种关键的翻译后修饰,参与调节广泛的细胞活动。然而,棉属(G. hirsutum)中磷酸化的位点及其在纤维细胞起始中的调控作用在很大程度上尚不清楚。在这项研究中,我们采用基于质谱的磷酸化蛋白质组学方法,对无绒短绒(fl)陆地棉(G. hirsutum)突变体及其同基因亲本野生型(WT)在授粉后-3 天和 0 天(DPA)的胚珠之间进行了全局和特异性磷酸蛋白质组谱分析。
通过 iTRAQ(相对和绝对定量的同重同位素标记)共鉴定到 830 个磷酸肽和 619 个磷酸蛋白中的 1592 个磷酸化位点。其中,使用 BLAST 程序在 P3DB 公共数据库中搜索后,首次鉴定到 76 个磷酸蛋白和 1100 个磷酸化位点。在所检测的磷酸肽中,在授粉后-3 天和 0 天的 fl 突变体与其 WT 的胚珠之间有 69 个差异表达。使用 Motif-X 程序进行的分析揭示了 19 个磷酸化基序,其中 8 个是棉花特有的。进一步的代谢途径分析表明,差异磷酸化蛋白参与信号转导、蛋白质修饰、碳水化合物代谢过程以及细胞周期和细胞增殖。
我们基于磷酸化蛋白质组学的研究提供了棉花纤维起始过程中磷酸化的首次全面概述,也为阐明 G. hirsutum 纤维发育中的信号网络提供了有用的数据集。