Proteomics, Interdisciplinary Center for Biotechnology Research, University of Florida Gainesville, FL, USA.
Proteomics, Interdisciplinary Center for Biotechnology Research, University of Florida Gainesville, FL, USA ; Department of Biology, UF Genetics Institute, University of Florida Gainesville, FL, USA.
Front Plant Sci. 2014 Feb 26;5:63. doi: 10.3389/fpls.2014.00063. eCollection 2014.
In maize developing seeds, transfer cells are prominently located at the basal endosperm transfer layer (BETL). As the first filial cell layer, BETL is a gateway to sugars, nutrients and water from mother plant; and anchor of numerous functions such as sucrose turnover, auxin and cytokinin biosynthesis/accumulation, energy metabolism, defense response, and signaling between maternal and filial generations. Previous studies showed that basal developing endosperms of miniature1 (mn1) mutant seeds lacking the Mn1-encoded cell wall invertase II, are also deficient for hexose. Given the role of glucose as one of the key sugars in protein glycosylation and proper protein folding; we performed a comparative large scale glycoproteome profiling of total proteins of these two genotypes (mn1 mutant vs. Mn1 wild type) using 2D gel electrophoresis and glycosylation/total protein staining, followed by image analysis. Protein identification was done by LC-MS/MS. A total of 413 spots were detected; from which, 113 spots matched between the two genotypes. Of these, 45 showed >20% decrease/increase in glycosylation level and were selected for protein identification. A large number of identified proteins showed decreased glycosylation levels in mn1 developing endosperms as compared to the Mn1. Functional classification of proteins, showed mainly of post-translational modification, protein turnover, chaperone activities, carbohydrate and amino acid biosynthesis/transport, and cell wall biosynthesis. These proteins and activities were related to endoplasmic reticulum (ER) stress and unfolded protein response (UPR) as a result of the low glycolsylation levels of the mutant proteins. Overall, these results provide for the first time a global glycoproteome profile of maize BETL-enriched basal endosperm to better understand their role in seed development in maize.
在玉米发育的种子中,转移细胞主要位于胚乳基部转移层(BETL)。作为第一个亲代细胞层,BETL 是母株糖、养分和水进入的门户;也是蔗糖周转、生长素和细胞分裂素生物合成/积累、能量代谢、防御反应以及母代和子代世代之间信号传递等众多功能的锚定点。先前的研究表明,缺乏 Mn1 编码的细胞壁转化酶 II 的微型 1(mn1)突变体种子的胚乳基部发育不良,也缺乏己糖。鉴于葡萄糖作为糖基化和正确蛋白质折叠的关键糖之一的作用;我们使用二维凝胶电泳和糖基化/总蛋白染色,随后进行图像分析,对这两种基因型(mn1 突变体与 Mn1 野生型)的总蛋白进行了大规模比较糖蛋白组分析。通过 LC-MS/MS 进行蛋白质鉴定。共检测到 413 个斑点;其中,113 个斑点在两种基因型之间匹配。其中,45 个斑点的糖基化水平增加/减少超过 20%,被选为蛋白质鉴定。大量鉴定出的蛋白质在 mn1 发育的胚乳中的糖基化水平比 Mn1 低。蛋白质的功能分类主要为翻译后修饰、蛋白质周转、伴侣活性、碳水化合物和氨基酸合成/转运以及细胞壁生物合成。这些蛋白质和活性与内质网(ER)应激和未折叠蛋白反应(UPR)有关,因为突变蛋白的糖基化水平较低。总的来说,这些结果首次提供了玉米 BETL 丰富的胚乳基部的全局糖蛋白组图谱,以更好地理解它们在玉米种子发育中的作用。