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本文引用的文献

1
Phosphoproteome analysis of B. cinerea in response to different plant-based elicitors.灰葡萄孢对不同植物源激发子响应的磷酸化蛋白质组分析。
J Proteomics. 2016 Apr 29;139:84-94. doi: 10.1016/j.jprot.2016.03.019. Epub 2016 Mar 18.
2
Proteomic profiling of Botrytis cinerea conidial germination.灰葡萄孢分生孢子萌发的蛋白质组学分析
Arch Microbiol. 2015 Mar;197(2):117-33. doi: 10.1007/s00203-014-1029-4. Epub 2014 Aug 21.
3
2-DE proteomic approach to the Botrytis cinerea secretome induced with different carbon sources and plant-based elicitors.利用 2-DE 蛋白质组学方法研究不同碳源和植物诱导子诱导的灰葡萄孢 secretome。
Proteomics. 2010 Jun;10(12):2270-80. doi: 10.1002/pmic.200900408.
4
Host-Pathogen Interactions: II. Parameters Affecting Polysaccharide-degrading Enzyme Secretion by Colletotrichum lindemuthianum Grown in Culture.宿主-病原体相互作用：II. 影响培养条件下菜豆炭疽病菌多糖降解酶分泌的参数
Plant Physiol. 1971 Jan;47(1):1-6. doi: 10.1104/pp.47.1.1.

不同植物源激发子诱导的磷酸化蛋白质组数据集。

Dataset of the phosphoproteome induced by different plant-based elicitors.

作者信息

Liñeiro Eva, Chiva Cristina, Cantoral Jesús M, Sabido Eduard, Fernández-Acero Francisco Javier

机构信息

Andalusian Center for Grape and Grapevine Research, CeiA3, Marine and Environmental Sciences Faculty, University of Cadiz, Puerto Real, 11510 Cádiz, Spain.

Proteomics Unit, Centre for Genomic Regulation (CRG), Dr. Aiguader, 88, 08003 Barcelona, Spain; Proteomics Unit, Universitat Pompeu Fabra (UPF), Dr. Aiguader, 88, 08003 Barcelona, Spain.

出版信息

Data Brief. 2016 Apr 22;7:1447-1450. doi: 10.1016/j.dib.2016.04.039. eCollection 2016 Jun.

DOI:10.1016/j.dib.2016.04.039
PMID:27761508
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5063813/
Abstract

Phosphorylation is one of the main post-translational modification (PTM) involved in signaling network in the ascomycete , one of the most relevant phytopathogenic fungus. The data presented in this article provided a differential mass spectrometry-based analysis of the phosphoproteome of under two different phenotypical conditions induced by the use of two different elicitors: glucose and deproteinized Tomate Cell Walls (TCW). A total 1138 and 733 phosphoproteins were identified for glucose and TCW culture conditions respectively. Raw data are deposited at the ProteomeXchange Consortium via the PRIDE partner repository with the data set identifier (PRIDE: http://www.ebi.ac.uk/pride/archive/projects/PXD003099). Further interpretation and discussion of these data are provided in our research article entitled "Phosphoproteome analysis of in response to different plant-based elicitors" (Liñeiro et al., 2016) [1].

摘要

磷酸化是子囊菌（一种最相关的植物病原真菌）信号网络中涉及的主要翻译后修饰（PTM）之一。本文所呈现的数据提供了基于差异质谱分析的在两种不同表型条件下的磷酸化蛋白质组分析，这两种条件是由使用两种不同的激发子诱导产生的：葡萄糖和脱蛋白番茄细胞壁（TCW）。分别在葡萄糖和TCW培养条件下鉴定出了总共1138个和733个磷酸化蛋白质。原始数据通过PRIDE合作伙伴存储库存于蛋白质组交换联盟，数据集标识符为（PRIDE: http://www.ebi.ac.uk/pride/archive/projects/PXD003099）。在我们题为“响应不同植物源激发子的[某种菌]磷酸化蛋白质组分析”（Liñeiro等人，2016年）[1]的研究文章中提供了对这些数据的进一步解读和讨论。