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小立碗藓发育重编程的磷酸化蛋白质组学分析

Phospho-proteomic analysis of developmental reprogramming in the moss Physcomitrella patens.

作者信息

Wang Xiaoqin, Zhou Sa, Chen Lu, Quatrano Ralph S, He Yikun

机构信息

Key Laboratory of Urban Agriculture (North) of Ministry of Agriculture, Beijing University of Agriculture, Beijing 102206, China; College of Life Sciences, Capital Normal University, Beijing 100048, China; Department of Biology, Washington University in St. Louis, MO 63130, USA.

College of Life Sciences, Capital Normal University, Beijing 100048, China.

出版信息

J Proteomics. 2014 Aug 28;108:284-94. doi: 10.1016/j.jprot.2014.05.012. Epub 2014 Jun 16.

Abstract

UNLABELLED

One of the most common post-translational modifications is protein phosphorylation, which controls many activities of plant life. However, its role in the reprogramming of developmental pathways of plant cells remains elusive. Here, using Physcomitrella patens, we characterize the phospho-proteome for protonemata, protoplasts made therefrom, and protoplasts regenerated for 2d. Through a titanium dioxide (TiO2)-based phospho-peptide enrichment method and liquid chromatography-tandem mass spectrometry (LC-MS/MS), more than 2000 phospho-proteins were identified. Among the 519 proteins with functional annotation in fresh protoplasts and protoplasts regenerated for 2d, proteins involved in epigenetic modification, post-transcriptional gene regulation, hormone signal transduction, and meristem maintenance have been previously reported to be important for developmental reprogramming. Several novel transcription factors including SWI/SNF complex protein, SNF2 family protein and MADS-domain transcription factor appear to be important in developmental reprogramming plant cells. Phosphorylation of marker proteins such as somatic embryogenesis receptor kinase and NAC transcription factor, suggests that this post-translational modification is vital for the cell's ability to adjust its developmental program. Together, our study presents a more complete understanding of the plant cell's developmental reprogramming.

BIOLOGICAL SIGNIFICANCE

Protoplast regeneration is an ideal model system for investigating developmental reprogramming in plants. Here, for Physcomitrella patens, we characterize the phospho-proteome for protonemata, protoplasts made therefrom, and for protonemata regenerated from the protoplasts for 2d. Among the 519 proteins with functional annotation in fresh protoplasts and protoplasts regenerated for 2d, proteins involved in epigenetic modification, post-transcriptional gene regulation, hormone signal transduction, and meristem maintenance have been reported to be important for expression of developmental reprogramming. Together, our study presents a more complete understanding of the plant cell's developmental reprogramming.

摘要

未标记

蛋白质磷酸化是最常见的翻译后修饰之一,它控制着植物生命的许多活动。然而,其在植物细胞发育途径重编程中的作用仍不清楚。在这里,我们利用小立碗藓,对原丝体、由其制备的原生质体以及再生2天的原生质体的磷酸化蛋白质组进行了表征。通过基于二氧化钛(TiO2)的磷酸化肽富集方法和液相色谱-串联质谱(LC-MS/MS),鉴定出了2000多种磷酸化蛋白质。在新鲜原生质体和再生2天的原生质体中具有功能注释的519种蛋白质中,先前已报道参与表观遗传修饰、转录后基因调控、激素信号转导和分生组织维持的蛋白质对发育重编程很重要。包括SWI/SNF复合蛋白、SNF2家族蛋白和MADS结构域转录因子在内的几种新型转录因子似乎在植物细胞发育重编程中很重要。体细胞胚胎发生受体激酶和NAC转录因子等标记蛋白的磷酸化表明,这种翻译后修饰对于细胞调整其发育程序的能力至关重要。总之,我们的研究对植物细胞的发育重编程有了更全面的了解。

生物学意义

原生质体再生是研究植物发育重编程的理想模型系统。在这里,对于小立碗藓,我们表征了原丝体、由其制备的原生质体以及从原生质体再生2天的原丝体的磷酸化蛋白质组。在新鲜原生质体和再生2天的原生质体中具有功能注释的519种蛋白质中,先前已报道参与表观遗传修饰、转录后基因调控、激素信号转导和分生组织维持的蛋白质对发育重编程的表达很重要。总之,我们的研究对植物细胞的发育重编程有了更全面的了解。

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