Department of Plant Genetics, Breeding and Biotechnology, Institute of Biology, Faculty of Biology and Biotechnology, Warsaw University of Life Sciences, Nowoursynowska 159, 02-776 Warsaw, Poland.
Department of Botany, Institute of Biology, Faculty of Biology and Biotechnology, Warsaw University of Life Sciences, Nowoursynowska 159, 02-776 Warsaw, Poland.
Int J Mol Sci. 2021 Nov 10;22(22):12147. doi: 10.3390/ijms222212147.
Cyst nematodes are important herbivorous pests in agriculture that obtain nutrients through specialized root structures termed syncytia. Syncytium initiation, development, and functioning are a research focus because syncytia are the primary interface for molecular interactions between the host plant and parasite. The small size and complex development (over approximately two weeks) of syncytia hinder precise analyses, therefore most studies have analyzed the transcriptome of infested whole-root systems or syncytia-containing root segments. Here, we describe an effective procedure to microdissect syncytia induced by from tomato roots and to analyze the syncytial proteome using mass spectrometry. As little as 15 mm of 10-µm-thick sections dissected from 30 syncytia enabled the identification of 100-200 proteins in each sample, indicating that mass-spectrometric methods currently in use achieved acceptable sensitivity for proteome profiling of microscopic samples of plant tissues (approximately 100 µg). Among the identified proteins, 48 were specifically detected in syncytia and 7 in uninfected roots. The occurrence of approximately 50% of these proteins in syncytia was not correlated with transcript abundance estimated by quantitative reverse-transcription PCR analysis. The functional categories of these proteins confirmed that protein turnover, stress responses, and intracellular trafficking are important components of the proteome dynamics of developing syncytia.
胞囊线虫是农业中重要的食草性害虫,它们通过称为合胞体的专门根结构获取营养。合胞体的起始、发育和功能是研究的重点,因为合胞体是宿主植物和寄生虫之间分子相互作用的主要界面。合胞体体积小且发育复杂(大约两周),这阻碍了精确分析,因此大多数研究都分析了受侵染的整个根系系统或含有合胞体的根段的转录组。在这里,我们描述了一种从番茄根中微分离由 诱导的合胞体并用质谱法分析合胞体蛋白质组的有效方法。从 30 个合胞体中切取的 15 毫米长、厚 10 微米的切片,每个样品中鉴定出 100-200 种蛋白质,这表明目前使用的质谱方法对植物组织的微观样品的蛋白质组分析具有可接受的灵敏度(约 100 微克)。在鉴定出的蛋白质中,有 48 种特异性存在于合胞体中,7 种存在于未感染的根中。这些蛋白质中约有 50%的存在与通过定量反转录聚合酶链反应分析估计的转录丰度无关。这些蛋白质的功能类别证实,蛋白质周转、应激反应和细胞内运输是发育合胞体蛋白质组动力学的重要组成部分。