Citrus phloem specific transcriptional profiling through the development of a citrus tristeza virus expressed translating ribosome affinity purification system.

IF 4.7 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
James N Culver, Meinhart Vallar, Erik Burchard, Sophie Kamens, Sebastien Lair, Yiping Qi, Tamara D Collum, Christopher Dardick, Choaa A El-Mohtar, Elizabeth E Rogers
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Abstract

Background: The analysis of translationally active mRNAs, or translatome, is a useful approach for monitoring cellular and plant physiological responses. One such method is the translating ribosome affinity purification (TRAP) system, which utilizes tagged ribosomal proteins to isolate ribosome-associated transcripts. This approach enables spatial and temporal gene expression analysis by driving the expression of tagged ribosomal proteins with tissue- or development-specific promoters. In plants, TRAP has enhanced our understanding of physiological responses to various biotic and abiotic factors. However, its utility is hampered by the necessity to generate transgenic plants expressing the tagged ribosomal protein, making this approach particularly challenging in perennial crops such as citrus.

Results: This study involved the construction of a citrus tristeza virus (CTV) vector to express an immuno-tagged ribosome protein (CTV-hfRPL18). CTV, limited to the phloem, has been used for expressing marker and therapeutic sequences, making it suitable for analyzing citrus vascular tissue responses, including those related to huanglongbing disease. CTV-hfRPL18 successfully expressed a clementine-derived hfRPL18 peptide, and polysome purifications demonstrated enrichment for the hfRPL18 peptide. Subsequent translatome isolations from infected Nicotiana benthamiana and Citrus macrophylla showed enrichment for phloem-associated genes.

Conclusion: The CTV-hfRPL18 vector offers a transgene-free and rapid system for TRAP expression and translatome analysis of phloem tissues within citrus.

柑橘韧皮部特异性转录谱通过柑橘tristeza病毒表达翻译核糖体亲和纯化系统的开发。
背景:分析翻译活性mrna或翻译组是监测细胞和植物生理反应的一种有用方法。其中一种方法是翻译核糖体亲和纯化(TRAP)系统,该系统利用标记核糖体蛋白分离核糖体相关转录物。该方法通过驱动带有组织或发育特异性启动子的标记核糖体蛋白的表达,实现了空间和时间基因表达分析。在植物中,TRAP增强了我们对各种生物和非生物因素的生理反应的理解。然而,由于需要产生表达标记核糖体蛋白的转基因植物,使得这种方法在诸如柑橘等多年生作物中尤其具有挑战性,因此其实用性受到阻碍。结果:构建了柑橘tristeza病毒(CTV)表达免疫标记核糖体蛋白(CTV- hfrpl18)的载体。CTV仅限于韧皮部,已被用于表达标记和治疗序列,使其适用于分析柑橘维管组织反应,包括黄龙冰病相关的维管组织反应。CTV-hfRPL18成功表达了克莱门汀衍生的hfRPL18肽,多体纯化证实了hfRPL18肽的富集。随后从受感染的本烟和大叶柑橘中分离出的翻译组显示韧皮部相关基因富集。结论:CTV-hfRPL18载体为柑橘韧皮部TRAP的快速表达和翻译组分析提供了一个无转基因的系统。
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
Plant Methods
Plant Methods 生物-植物科学
CiteScore
9.20
自引率
3.90%
发文量
121
审稿时长
2 months
期刊介绍: Plant Methods is an open access, peer-reviewed, online journal for the plant research community that encompasses all aspects of technological innovation in the plant sciences. There is no doubt that we have entered an exciting new era in plant biology. The completion of the Arabidopsis genome sequence, and the rapid progress being made in other plant genomics projects are providing unparalleled opportunities for progress in all areas of plant science. Nevertheless, enormous challenges lie ahead if we are to understand the function of every gene in the genome, and how the individual parts work together to make the whole organism. Achieving these goals will require an unprecedented collaborative effort, combining high-throughput, system-wide technologies with more focused approaches that integrate traditional disciplines such as cell biology, biochemistry and molecular genetics. Technological innovation is probably the most important catalyst for progress in any scientific discipline. Plant Methods’ goal is to stimulate the development and adoption of new and improved techniques and research tools and, where appropriate, to promote consistency of methodologies for better integration of data from different laboratories.
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