Temporal wheat proteome remodeling by deoxynivalenol reveals novel detoxification signatures and strategies across cultivars.

IF 6.1 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Reid Buchanan, Kholoud Shaban, Boyan Liu, Norris Chan, Mitra Serajazari, Jennifer Geddes-McAlister
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引用次数: 0

Abstract

Fusarium head blight (FHB) is a globally devastating fungal disease resulting in reduced grain yield and quality, along with contamination of grains with dangerous mycotoxins. Consumption of such mycotoxins by humans through processed food or livestock through feed has downstream implications for human and animal health. This interconnectivity across the environment, animal, and human health defines the One Health problem of threatened food safety and security. In this study, we explore remodeling of the wheat proteome upon exposure to a common mycotoxin, deoxynivalenol (DON). We investigate cultivar-specific responses to DON exposure in FHB-susceptible (Norwell) and -resistant (Sumai#3) cultivars across a continuum of exposure (i.e., 24 and 120 hours post inoculation), and upon low (i.e., 0.1 mg/mL) and high (1.0 mg/mL) levels of the mycotoxin. This complex experimental design enables us to tease apart the dynamic relationship between each cultivar and DON tolerance. Specifically, we define precise proteins and broad categories of remodeling that are common (i.e., reduction in photosynthesis) and exclusive (i.e., glycosyltransferase) to the cultivars and align with anticipated protective mechanisms. Moreover, we adapted an in vitro DON tolerance expression system and determined that induction of an ubiquinol oxidase (UniProt ID: A0A3B6B5K8) provides heightened protection for yeast growth relative to the negative control, as well as increased protection compared to a well-defined DON detoxifying protein. Our study suggests a new avenue for identification and characterization of novel DON detoxifying proteins as putative biomarkers for selected breeding strategies. Such strategies support the production of wheat varieties with increased tolerance to DON for improved global food safety and security.

脱氧雪腐镰刀菌醇对小麦蛋白质组的时间重塑揭示了不同品种间新的解毒特征和策略。
赤霉病是一种全球性的破坏性真菌疾病,导致粮食产量和质量下降,并使粮食受到危险真菌毒素的污染。人类通过加工食品或牲畜通过饲料摄入这类真菌毒素,会对人类和动物健康产生下游影响。环境、动物和人类健康之间的这种相互联系定义了受威胁食品安全和保障的“同一个健康”问题。在这项研究中,我们探讨了小麦蛋白质组暴露于一种常见的霉菌毒素脱氧雪腐镰刀菌醇(DON)后的重塑。我们研究了fhb敏感(Norwell)和耐药(Sumai#3)品种在连续暴露(即接种后24和120小时)以及低(即0.1 mg/mL)和高(1.0 mg/mL)真菌毒素水平下对DON暴露的品种特异性反应。这种复杂的实验设计使我们能够梳理出每个品种与DON耐受性之间的动态关系。具体来说,我们定义了精确的蛋白质和广泛的重塑类别,这些重塑是常见的(即光合作用减少)和专有的(即糖基转移酶),并与预期的保护机制保持一致。此外,我们采用了体外DON耐受表达系统,并确定与阴性对照相比,诱导泛醇氧化酶(UniProt ID: A0A3B6B5K8)对酵母生长提供了更高的保护,与明确定义的DON解毒蛋白相比,也提供了更高的保护。我们的研究为鉴定和表征新的DON解毒蛋白作为选择育种策略的推定生物标志物提供了新的途径。这些战略支持生产对DON耐受性更高的小麦品种,以改善全球食品安全和保障。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular & Cellular Proteomics
Molecular & Cellular Proteomics 生物-生化研究方法
CiteScore
11.50
自引率
4.30%
发文量
131
审稿时长
84 days
期刊介绍: The mission of MCP is to foster the development and applications of proteomics in both basic and translational research. MCP will publish manuscripts that report significant new biological or clinical discoveries underpinned by proteomic observations across all kingdoms of life. Manuscripts must define the biological roles played by the proteins investigated or their mechanisms of action. The journal also emphasizes articles that describe innovative new computational methods and technological advancements that will enable future discoveries. Manuscripts describing such approaches do not have to include a solution to a biological problem, but must demonstrate that the technology works as described, is reproducible and is appropriate to uncover yet unknown protein/proteome function or properties using relevant model systems or publicly available data. Scope: -Fundamental studies in biology, including integrative "omics" studies, that provide mechanistic insights -Novel experimental and computational technologies -Proteogenomic data integration and analysis that enable greater understanding of physiology and disease processes -Pathway and network analyses of signaling that focus on the roles of post-translational modifications -Studies of proteome dynamics and quality controls, and their roles in disease -Studies of evolutionary processes effecting proteome dynamics, quality and regulation -Chemical proteomics, including mechanisms of drug action -Proteomics of the immune system and antigen presentation/recognition -Microbiome proteomics, host-microbe and host-pathogen interactions, and their roles in health and disease -Clinical and translational studies of human diseases -Metabolomics to understand functional connections between genes, proteins and phenotypes
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